HEMATOLOGY

1. Caryopreciptate contains all of the following

except:
a. f VIII.
b. vWF
c. f V.
d. f XIII.
2. Thin blood film important in :
a. WBCs count
b. RBCs c0unt
c. Reticulocyte count#
d. Presence of sickle cell in blood
3. 3-FFP ALL CORRECT except:
a. storage 20-24c#
b. correct factors deficiency
c. storage period 12 month in -18c
d. resolve the effect of waffarin
4. Patient treated with heparin,which test
prolonged:
a-bleeding
b-PTT #
c-PT,.
5. All of these patient can't donate blood except:
a. fever
b. diarrhoea
c. Iron deficiency anaemia
d. HIV
6. temperature of storage platelets:
a. 15-20 C
b. 22-30 C #
c. 30-45 C
d. 37-50 C
140
7. worm antibody:
A- IgM
B- IgG #
C- IgA

8. these people can donate blood except:

A-blood pressure 130\90
B- Hb in male above 13 mg\dl
C-age above 18 years old
D-pregnant woman #
9. RBCs are destroyed by
A- RES #
B-plasma cell
C-NK-cells
10. international receptor from all blood groups:
a. group O Rh ve
b. group O Rh +ve
c. group AB Rh ve
d. group AB Rh +ve #
11. If father& mother have sickle cell trait What's
the like hood of the disease in
children:
a. 0%
b. 25% #
c. 50%
d. 100%
12. abnormal homozygotes (HbSS) diagnosed by:
A-hemoglobin electrophoresis #
B- gram stained smear
C-
13. PCV divided by RBC this is calculation of :
A- MCV#
B-MCH
C-MCHC
141
D-Hb
14. The serum antibodies that can be found in
individuals in O group is\are :
a. Anti A and B
b. Anti B only
c. Anti A only
d. None of the above

15. Life spin of red blood cell is;

a. 120 days
b. 40 days.
c. 180 days.
d. 1 day.
16. The general blood donor is :
a. A blood group.
b. B blood group.
c. O blood group.
d. AB blood group.
17. A person with A blood group can receive blood
from:
a. A blood group donor.
b. B blood group donor.
c. O blood group donor.
d. 1 AND 3
18. alpha thalathemia is:
a. alpha chain synthesis defect
b. gamma chain synthesis defect
c. beta hain synthesis defect
d. delta chain synthesis defect
19. iron deficiency anemia
a. Microcytic
b. macrocytic
142
c. normocytic
d. normochromic
20. philadelphia chromosome
a. AML
b. CLL
c. CML
d. ALL
21. ABO blood group include
a. a&b&o
b. a&b&o&ab
c. a&b&ab
d. a&b e-o

22. when we prepare FFP:

a. immediately
b. after 4 hrs
c. after6 hrs
d. any time before bag expired
23. which of tge following not made leucocyte
a. neutrophil
b. eosinophil
c. basophil
d. macrophage
24. Iron absorpstion in
a. duodenum
b. jejunum
c. stomach
25. to managed of sickle cell anaemia
a. chemotherapy
b. radiotherapy
c. folic acid
143
26. Increase lymphocyte in
a. acute leukaemia
b. cml
c. cll
27. anaemia diagnosis depend on
a. HB
b. RBC
c. red cell indices
d. HB electrophoresis
28. Plasma differ from serum due to contain:
a. fibrin
b. fibrinogen
c. plasminogen
d. thrombin
29. temperature of storage platelets:
a. 15-20 C
b. 22-30 C
c. 30-45 C

d. 37-50 C
30. these people can donate blood except:
a. blood pressure 130\90
b. Hb in male above 13 mg\dl
c. age above 18 years old
d. pregnant woman
31. international receptor from all blood groups:
a. group O Rh ve
b. group O Rh +ve
c. group AB Rh ve
d. group AB Rh +ve #
144
32. Systemic Lupus Erythromatosus diagnosed by:
a. heterophil antibody test
b. antinuclear antibody test
c. bence jones protein
d. examining giemsa stained smear
33. if fother& mother have sickle cell trait What's
the likely hood of the disease in children:
a. 0%
b. 25%
c. 50%
d. 100%
34. The main (most) Hb found in adult is:
a. Hb A
b. Hb A2
c. Hb F
35. Rh-ve patient means he dose not have:
a. E antigen
b. D antigen
c. B antigen
d. C antige
36. Heparin is:
a. Protein
b. Enzyme
c. Polysaccharide
d. Oligosaccharide

145
37. Thrombin time is:
a. Check for Extrinsic coagulation pathway (factors)
b. Intrinsic coagulation pathway (factors)
c. The conversion of prothrombin to fibrinogen in
addition of thrombin
38. ALL CELLS ARE NUCLEATED EXCEPT :a. LYMPH
b. MONOCYTES
c. RBCS
d. NEUTROPHIL
39. Thrombocytopenia case found in :
a. Aplastic anemia
b. Acetyl lymphoid leukemia
c. Hemorrhage
40. Lymphocytosis find in case of :
a. infection
b. virus
c. bacterial
d.
41. In parasitic infection, increase :
a. Eosinophil
b. basophile.
c. lymphocyte
42. PCV with total of RBCs, called :
a. MCV
b. MCH
c. MCHC
43. MCV 104 fl , vitaminB12 and folate are normal
a. Iron deficiency anemia
146
b. liver cirrhosis
c. auto haemolytic anemia
d. vitamin E deficiency
e. sideroblastic anemia.
44. father B blood G Mother A
a. 25%

b. 50%
c. 75%
d. 100%
45. patient with O Blood G What The safly blood g
we can donat
a. O
b. B
c. AB
d. A
46. Which if the following leukocyte normally not
found in blood film?
a. Basophile
b. Monocyte
c. Lymphocyte
d. Neutrophils
e. Eosinoph
47. Largest cells in blood film
a. Monocyte
b. Lymphocyte
C. Neutrophil
D. Eosinophil
48. Universal donor is :
a. O+?
b. Oc.
AB
d. A+
147
49. When analysis anemia of normocytic
normochromic to exclude hemolytic we
do :
a. CBC
b. Ferritin
c. Transferrin
d. Soluble transferrin
50. Decrease neutrophil , lymphocyte , :
a. Pure red cell aplasia )
b. Aplastic anemia

d. All of the above

51. Retics normal range in adult is :
a. 1-5
b. 0.1-0.2
c. 0.2-5
d. 0.2-2 %
52. ESR anticoagulant is :
a. EDTA
b. Sod-citrate
c. Sod-citrate + heparin
d. Li-heparin
53. Rh antigens are:
a. D, C, c, E, and e
b. D, d , C, c, E and e
c. d,C,c,E and e
d. D,d,C,c and e
54. which factor cause pt prolong:
a. IX
b. XII
c. XI
d. VIII
148
55. the evidence of anemia
a. Hb #
b. prephral blood picture
c. electrophoresis
56. plasma iron bind with :
a.ferritin
b.transferrin
c.haptoglobin
57. transmitter through blood transfusion ?
a. AIDS
b. Malaria
c. Cytomegalovirus
d. All above
58. Philadelphia chromosome is diagnostic for:
a. acute lymphoblastic leukemia

b.Acute myeloid leukemia

c. Chronic lymphocytic leukemia
d.chronic myeloid leukemia#
59. low megakarucyte in B.M found in :
a. A plastic anaemia
b. disseminated intravascular coagylation
c. idiopathic thrombocytopenic purpra(
d. thrombotic thrombocutopenic pyrpura(
60. MCV elevate in all except :
a. Iron diffiecincy anaemia
b. Megaloplastic anaemia
c. Pernicious anaemia
149
61. polymorphic non nucleated cell in blood :
a. Retic
b. Rbcs
c. Promylocye
d. Plts
62. ANTIBODY FOUND IN BLOOD GROUP AB
INDIVIDUALS :
a. ANTI-A
b. ANTI-AB
c. ANTI-B
d. NONE
63. Neutrophil is acommn White blood cell present
in blood and the percentage of
presence is :
a. 90%
b. 15%
c. 75%
64. Iron containing protein is
a. Thyroglbulin
b. Albumin
c. Hemoglobin
d. Globulin
e. Insulin

65. Hemophilia "A" man married to normal female

the incidence of his children
will be
a. Male carrier
b. Female carrier
c. Disease male
d. Disease girls
e. Normal all
150
66. The best useful test to differential between
Hemophilia "A" from Hemophilia
"B"
a. PTT
b. PT
c. Inheritance studies
67. Vitamin required for blood coagulation
a. Vitamin K
b. Pyridoxine
c. Vitamin E
d. Vitamin D
e. Pantothenic acid
68. In purpura
a. Hge in deep muscles
b. He in mucus membrane
c. Haemarthrosis
69. Blood donor in K.S.A. are all of the following
except
a. Hb% 12.5 - 16
b. Free from syphilis
c. Jaundice free
d. One year after delivery
70. Variation in RBCs size is
a. Macrocytosis
151
b. Anisocytosis
c. Microcytosis
d. Polychromasia

71. pretransfusion test that is performed using the

patient red cells and donor
plasma
a. Major x-matching
b. Minor x-matching
c. Antibody screen
d. Non of the above
72. Blood transfusion can transmit:
a. HIV
b. CMV
c. Hepatitis B virus
d. All of the above.
73. Estimation of G6PDH is a test to
a. Measure blood glucose
b. To diagnose hemolytic anemia
c. To diagnostic myocardial infraction
d. To diagnostic pancreatic disease
74. To measure G6PDH we use
a. Plasma
b. Whole blood
c. Serum
152
d. All of the above
75. variation in RBCs size?
a. microcytosis
b. macrocytosis
c. aniso cytosis
76. tests for platelets function includes :a. Bleeding time
b. RBCs count
c. WBCs count
d. Platelets count
77. causes of thrombocytosis includes
a. hemorrhage
b. hemolysis
c. trauma
d. all of the above

78. The end product of coagulation is

a. fibrinogen clot
b. prothrombin clot
c. fibrin clot
d. all of the above
79. The natural anticoagulant include
a. anti thrombinIII
b. protein C
c. protein S
d. all of the above
80. Synthesis of prothrombin group need to
a. vitamin A
b. vitamin K
c. vitamin D
153
d. vitamin B12
81. Causes of vitamin K deficiency include:
a. increase intake
b. increase utilization
c. decrease absorption
d. all of the above
82. hemophilia B which is caused by deficiency in
a. factor V
b. factor III
c. factor IX
d. factor VIII
83. hemophilia A which is caused by deficiency in
a. factor IX
b. factor VIII
c. factor IV
d. factor V
84. .are group of disorders
characterized by accumulation
malignant white cells in bone marrow& blood
a. leukemia
b. neutrophilia
c. DIC

d. neutropenia
85. Increase of total circulating leukocytes is called
a. leukocytopenea
b. leukocytosis
c. neutrophilia
d. neutropenia
86. Theis a reactive & excessive
leukocytosis usually characterized
by the presence of immature cells
154
a. leukocytosis
b. basophilia
c. Leukaemoid Reaction
d. lymphocytosis
87. The normal distribution of eosinophils is about
a. 1- 4 %
b. 4- 8 %
c. 10- 22%
d. 40-70 %
88. The normal distribution of basophils is about
a. 4- 8 %
b. 0- 1 %
c. 10- 15%
d. 40-75 %
89. The normal distribution of monocyte is about
a. 0- 1 %
b. 10- 12%
c. 40- 45%
d. 4- 8 %
90. abnormal bleeding may result from
a. neutrophilia
b. basophilia
c. thrombocytopenia
d. leukocytosis
91. causes of prolonged prothrombin time is.
a. vitamin K deficiency
b. some liver disease

c. factor V deficiency
d. all of the above
155
92. pathological causes of neutrophilia include
a. bacterial infection
b. new born
c. during pregnancy
d. delivery
93. heparin it is found in mast cells and..
a. Neutrophilia
b. Eosinophil
c. Basophils
d. all of the above
94. the clinical features of multiple myloma is
a. bone pain
b. malaria
c. night fever
d. nausia
95. the laboratory finding of lymphoma include
a. normocytic normochromic anemia
b. neutrophilia
c. ESR and CRB are raised
d. all of the above
96. neutropenia is seen in the following :
a. bacterial infection
b. viral infection
c. blood disease
d. all of the above
97. ( DIC ) means :
a. disseminated intra vascular coagulation
b. distructer intra vascular coagulation
c. detective intra vascular coagulation
d. decrease intra vascular coagulation
156
98. (VWF) means :
a. von willebrand female
b. volume willebrand disease

c. von wound factor

d. von willebrand factor
99. One of hemophilia types is
a. hemophilia K
b. hemophilia B
c. hemophilia N
d. hemophilia O
100. The normal range of prothrombin time ( PT ) is
:a. 12 15 sec
b. 20 25 sec
c. 5 10 sec
d. 7 9 sec
101. The normal range of Activated partial
thromboplastin time (APTT) is :a. 20 30 sec
b. 10 20 sec
c. 15 25 sec
d. 30 40 sec
102. all of the following is the natural anti
coagulant except
a. antithrombin III
b. warfarin
c. protein C
d. protein S
103. the acceptable minimum concentration of
heamoglobin for the donor is:
a. 12-15 g/dl
b. 10-5 g/dl
c. 9.5 g/dl
d. 15.5 g/dl
157
104. all of these are adverse donor reaction except
:
a. syncope
b. convulsions
c. hypertension

d. nausea and vomiting

105. the platelet are stored at :
a. 2 :6 c b. 20 :26 c c. 20 :50 c d. 120 :180 c
106. major cross match:
a. donors cells +patient serum
b. donors serum +patients cell
c. donors cells +donors serum
d. patients cells +patients serum
107. cold agglutination syndrome is due to :
a. IgG
b. IgM
c. IgA
d. Ig D
108. type of antibody is
a. IgA
b. IgG
c. IgM
d. all the above
109. secondary auto immune hemolytic anemia
include
a. viral infection
b. malaria
c. Typhoid
d. non the above
158
110. the procedure of cross matching is
a. saline technique
b. blood technique
c. major technique
d. miner technique
111. found in RBCS surface
a. antigen
b. antibody
c. a &b
d. all the above
112. ..found in serum
a. antigen

b. antibody
c. a &b
d. non of the above
113. Rh system include
a. D
b. A
c. H
d. N
114. the red cell freezing at .using liquid
nitrogen for 3 years
a. 190co
b. 37 co
c. 30 co
d. 40 co
115. the blood transfusion therapy include
a. RBCS & platelet
b. therapy
c. nitrogen
d. non the above
159
116. what is the type of donor
a. volunteer blood donor
b. Immunogene
c. hapaten
d. d-Adjuvant
117. keep the bag with red cells at
a. 4- 8 co
b. 4-6 co
c. 10 -13 co
d. 30 -40 co
118. store the plasma bag at
a. 70 co
b. 30 co
c. 40 co
d. 50 co
119. mean cell volume means
a. MCV

b. MCH
c. MCHC
d. all the above
120. what is the first blood group system was
discovered in 1901
a. Rh blood group system
b. ABO blood group system
c. duffy blood group system
d. KIDD blood group system
121. the only Ig that can cross the placenta:
a. IgE
b. IgD
c. IgM
d. IgG
160
122. Antibodies are secreted from:
a. B-lymphocyte
b. T-lymphocyte
c. monocyte
d. Macrophage
123. immunity through placenta is:
a. natural active immunity
b. Artificial active immunity
c. Natural passive immunity
d. Artificial passive immunity
124. the platelet are stored at :
a. 2 :6 c b. 20 :26 c c. 20 :50 c 125. the color of
anti-sera A:
a. yellow
b. colorless
c. blue
d. green
126. the color of anti-sera B is:
a. red
b. blue
c. yellow
d. colorless

127. patient with anti A antibodies in his serum ,his

blood group is :
a. group A
b. group B
c. group AB
d. group O
161
128. the red cells of a patient with neither A nor B
antigen on the surface ,his
blood group is
a. group A
b. group B
c. group AB
d. group O
129. duffy blood group like
a. ABO group
b. Kidd
c. Rh blood group
d. MNS blood group
130. blood group can be done by
a. slide method
b. centrifuged
c. auto cleave
d. allthe above
131. the blood donor must not be less than:
a. 30 years
b. 18 years
c. 40 years
d. 25 years
132. the clinical significance of Rh antigen :
a. blood transfusion
b. hemolytic disease of newborn
c. medical legal
d. all of the above
133. incomplete antibody :
a. IgM
b. IgA

c. Ig G
d. Ig D
162
134. in cross matching we use:
a. albumin
b. antihuman globulin
c. papain enzyme
d. all of the above
135. the temperature of the blood refrigerator is:
a. 6 9C b. 2 6 C c. 9 15 C d. 20 25 C
136. biochemical changes in the stored blood
RBCs:
a. RBCs change its shape
b. osmotic fragility is increased
c. loss of red cell membrane lipids
d. all of the above
137. the red cells in frozen state can be stored for
years by addition of:
a. oxygen
b. hydrogen
c. nitrogen
d. glycerol
138. dark red card on blood bag means:
a. group O +ve
b. group A +ve
c. group B +ve
d. group AB +ve
139. panel test is done to know:
a. viruses on the serum
b. antigen on the serum
c. antibodies on the serum
163
d. all of the above
140. complete antibody :
a. IgM
b. IgA
c. Ig G

d. Ig D
141. the ratio of the volume of cellular elements to
that of whole blood is:
a. MCV
b. MHC
c. MCHC
d. HCT
142. the normal value of mean corpuscular volume
is:
a. 27 32 pg
b. 80 90 fl
c. 33 38 %
d. non of the above
143. (PCV/RBCs count ) =
a. MCH
b. MCHC
c. MCV
d. HCT
144. the degradation of heme takes place in the
.particularly in the liver
and spleen
a. reticulocytes
b. erythrocytes
c. reticuloendothelial cells
d. non of the above
145. its function is to transport oxygen from the
lung to the tissue:
a. haptoglobin
164
b. hemoglobin
c. bilirubin
d. myoglobin
146. other blood groups include
a. ABO group
b. duffy blood group
c. a& b
d. non the above

147. life span of RBCS

a. 120 days
b. 150 days
c. c 170 days
d. d non of the above
148. -------------- have a lobulated nucleus , appear
very pale pink in stained
smear and elimination of bacteria by using
enzymes .
a. Neutrophiles
b. Eosinophiles
c. Lymphocytes
d. Basophiles
149. If RBCs are lost through bleeding or destroyed
too rabidly , RBCs
production in the --------------------- is stimulated .
a. Stomach
b. Bone marrow
c. Intestine
d. Non of above
150. The average number of WBCs is
-----------------which are categorized as
granulocytes and agranulocytes .
a. 2 - 4 _ 105 / mm3
b. 2 - 4 _ 108 / mm3
c. 4 - 11 _ 103 / mm3
d. Non of above
165
151. - -------------- have a characteristic bilobed
nucleus, their cytoplasm filled
with large , refractile granules that stain red in
blood smear .
a. Neutrophiles
b. Eosinophiles
c. Lymphocytes
d. Basophiles

152. The sedimented erythrocytes ( RBCs )

constitute about ----------------of
blood volume .
a. 45 %
b. 55 %
c. 75 %
d. 95 %
153. The initial exposure to the Rh antigen during
the first pregnancy does
not cause erythroblastosis fetalis because ---------is produced and cannot cross
the placenta .
a. Ig M
b. Ig G
c. Ig E
d. Non of above
154. Acute blood loss usually results in a
------------------ anemia , which is
dramatic and often traumatic .
a. Normochromic
b. Normocytic
c. Hypochromic
d. ( a & b )
155. -------------- their nucleus is kidney-shaped or
oval and act as macrophages
for bacterial phagocytosis and clean-up dead cell
debris .
a. Neutrophiles
b. Eosinophiles
c. Monocytes
d. Basophiles
166
156. - ------------ promotes blood clotting and help to
prevent blood loss from
damaged blood vessels.
a. R.B.Cs
b. W.B.Cs

c. Platelets
d. Anemia
157. ---------- is the prototype of the congenital
hemoglobinopathies and the
abnormal hemoglobin is designated Hb S.
a. Thalassemia
b. G6PD
c. Sickle cell
d. Non of above
158. The normal adult blood volume measures
-------------------a. 7 9 L
b. 3 5 L
c. 5 6 L
d. Non of above
159. The symptoms of ----------------- is shown as
pallor of skin , increased
pulse rate , palpitations , dizziness and fatigue .
a. Acute anemia
b. Sever anemia
c. Chronic anemia
d. ( a & b )
160. ----------- is a specialized connective tissue
consisting of cells and plasma .
a. The cell
b. Blood
c. Plasma
d. Serum
167
161. ------------------- a reduction in the number of
platelets in blood leads to
increased susceptibility to bleeding .
a. Leukocytopenia
b. Erythrocytopenia
c. Thrombocytopenia
d. Non of above

162. ------------------It contains erythrocytes

( RBCs ),leukocytes ( WBCs ) and
platelets . which sitting on the top of the
erythrocytes layer .
a. Sediment
b. Supernatant
c. Buffy coat
d. Non of above
163. The --------------- fraction above the packed
RBCs consists of plasma .
a. Sediment
b. Supernatant
c. Buffy coat
d. Non of above
164. -------- is the fluid component of blood , it
contains salts and organic
compounds.
a. The cell
b. Blood
c. Plasma
d. Serum
165. In the absence of anticoagulant , the fluid
portion of blood is called
--------------- , which is essentially fibrinogen free
plasma .
a. The cell
b. Blood
c. Plasma
d. Serum
168
166. The blood smear gives the physician
information concerning ----------a. Morphology of the RBCs and platelets
b. Presence of abnormal inclusion bodies
c. Immature cell types
d. All of above

167. ----------- they are non nucleated , biconcave

shaped cells , lake
organelles and consist of a plasma membrane .
a. Erythrocytes
b. Leukocytes
c. Platelets
d. Non of above
168. -------------- is the reduction in the amount of
circulating Hb , RBCs , or
both .
a. Erythrocytes
b. Leukocytes
c. Platelets
d. Anemia
169. ------------------- is red cell enzyme defect , the
affected persons are often
women who are susceptible to drugs .
a. Thalassemia
b. G6PD
c. Sickle cell
d. Non of above
170. -------------- asymmetric, unequal long
projections from the red cell
surface , often with small bulbous ends and seen in
liver disease
a. Ovalocyte
b. Elliptocyte
c. Acanthocyte
d. Echinocyte
169
171. - ------------------ is an antibody induced
hemolytic disease in the
newborn that is caused by blood group
incompatibility between mother and
fetus .
a. Erythroblastosis fetalis
b. Spherocytosis

c. Pernicious anemia
d. Non of above
172. The -------------- is the primary site responsible
for the destruction of
elliptocytes and spherocytes .
a. Liver
b. Bone marrow
c. Spleen
d. Non of above
173. Subsequent exposure to D antigen during the
second or third pregnancy
leads to a strong ------------ response (which can
cross placenta)
a. Ig M
b. Ig G
c. Ig E
d. Non of above
174. -------------------is a failure or decrease in
synthesis of the B-chain of
hemoglobin and RBCs are deformed and
hypochromic .
a. Thalassemia
b. G6PD
c. Sickle cell
d. Non of above
175. --------------- it is a curved cell with sharp ends
and seen in congenital
hemoglobinopathies ( Hb S )
a. Ovalocyte
b. Elliptocyte
c. Acanthocyte
d. Sickle cell
170
176. -------------------is a failure or decrease in
synthesis of the hemoglobin
molecule and RBCs are deformed and hypochromic
.

a. Thalassemia
b. G6PD
c. Sickle cell
d. Non of above
171
HEMATOLOGY ANSWER
181. C
182. C
183. A
184. B
185. B
186. B
187. B
188. D
189. A
190. D
191. B
192. A
193. A
194. A
195. A
196. C
197. D
198. A
199. S
200. C
201. B
202. A
203. D
204. A
205. C
206. C
207. A
208. B
209. B
210. D
211. B

212.
213.
214.
215.
216.
217.
218.
219.
220.
221.
222.
223.
224.
225.
226.
227.
228.
229.
230.
231.
172
232.
233.
234.
235.
236.
237.
238.
239.
240.
241.
242.
243.
244.
245.
246.
247.

B
B
A
B
C
A
C
A
B
A
A
B
A
A
A
A
B
A
B
D
B
A
A
A
B
D
D
A
A
D
D
C
C
B
C
A

248.
249.
250.
251.
252.
253.
254.
255.
256.
257.
258.
259.
260.
261.
262.
263.
264.
265.
266.
267.
268.
269.
270.
271.
272.
273.
274.
275.
276.
277.
278.
279.
280.
281.
282.
283.
284.

B
D
B
B
D
B
B
C
A
D
C
D
B
C
C
B
A
B
C
A
B
D
C
D
A
C
A
D
B
A
D
B
A
D
B
A
C

285.
173
286.
287.
288.
289.
290.
291.
292.
293.
294.
295.
296.
297.
298.
299.
300.
301.
302.
303.
304.
305.
306.
307.
308.
309.
310.
311.
312.
313.
314.
315.
316.
317.
318.
319.
320.

B
A
B
D
A
A
A
B
A
A
A
A
B
B
A
B
D
A
C
B
C
C
B
D
B
A
B
D
C
D
B
D
D
A
C
A

321.
322.
323.
324.
325.
326.
327.
328.
329.
330.
331.
332.
333.
334.
335.
336.
337.
338.
339.
174
340.
341.
342.
343.
344.
345.
346.
347.
348.
349.
350.
351.
352.
353.
354.
355.
356.

D
B
C
C
B
B
A
A
B
C
B
A
A
D
C
C
C
C
D
B
C
C
B
C
D
D
A
D
B
C
A
C
B
A
D
A

175