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1.
G-6-PD deficiency in newborns.
Handa, V; Mukherjee, R A; Patel, R Z; Oza, R M.
J Indian Med Assoc ; 1985 Jul; 83(7): 225-6
Article in English | IMSEAR | ID: sea-96898

Subject(s)
Bilirubin/blood , Glucosephosphate Dehydrogenase Deficiency/complications , Humans , India , Infant, Newborn , Jaundice, Neonatal/etiology
2.
The Oh (Bombay group) phenotype.
Handa, V; Oza, R M; Patel, R Z; Zanzarukiya, B B; Mukherjee, R A.
J Indian Med Assoc ; 1984 Dec; 82(12): 446-7
Article in English | IMSEAR | ID: sea-96347

Subject(s)
ABO Blood-Group System/genetics , Adolescent , Humans , Phenotype
3.
Hemoglobin electrophoresis in agar gel--a modified method for routine use.
Giri, D D; Patra, S B; Patel, R Z.
Indian J Pathol Microbiol ; 1984 Jul; 27(3): 179-83
Article in English | IMSEAR | ID: sea-72743

Subject(s)
Blood Protein Electrophoresis/methods , Electrophoresis/methods , Electrophoresis, Agar Gel/methods , Hemoglobins/analysis , Hemoglobins, Abnormal/analysis , Humans , Hydrogen-Ion Concentration
4.
Hemoglobinopathies in childhood (a study of 51 cases).
Giri, D D; Patra, S B; Patel, R Z.
Indian J Pathol Microbiol ; 1984 Apr; 27(2): 81-9
Article in English | IMSEAR | ID: sea-74231

Subject(s)
Adolescent , Anemia, Hemolytic/epidemiology , Child , Child, Preschool , Female , Hemoglobinopathies/epidemiology , Hemoglobins, Abnormal/analysis , Humans , India , Infant , Infant, Newborn , Male
5.
Double heterozygous hemoglobinopathies--diagnostic importance of parent studies.
Patra, S B; Giri, D D; Patel, R Z; Modi, U J; Amin, N S.
Indian Pediatr ; 1983 Jul; 20(7): 485-8
Article in English | IMSEAR | ID: sea-13115

Subject(s)
Anemia, Sickle Cell/genetics , Child , Hemoglobin E/genetics , Hemoglobinopathies/genetics , Hemoglobins, Abnormal/genetics , Genetic Carrier Screening , Humans , Parents
6.
HbE-beta thalassemia.
Giri, D D; Patra, S B; Patel, R Z; Modi, U J; Amin, N S.
Indian Pediatr ; 1982 Dec; 19(12): 1031-4
Article in English | IMSEAR | ID: sea-14561

Subject(s)
Child, Preschool , Electrophoresis, Agar Gel , Hemoglobin E/genetics , Hemoglobins, Abnormal/genetics , Humans , Male , Thalassemia/genetics
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