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Biomedical subjects

H M Bhatia

Publications and source records attributed to H M Bhatia.

At least 73 records · Page 4Linked to original sources
PubMed1979

A new red cell phenotype I-i-: red cells lacking both I and i antigens.

When blood samples from 5,864 healthy Indian blood donors were tested with anti-I, seven samples failed to react or reacted only weakly. Further studies with a number of anti-I and anti-i sera suggested that these samples had the phenotype I-i- and reacted weakly with anti-IT. In one family, the I-i- phenotype was present in three generations.

Absorption↗
PubMed1979

Distribution of subtypes of hepatitis B surface antigen in Western India.

HBsAg subtype distribution of 105 positive samples showed 91.4% as ay type. The ay was predominant in different disease conditions, healthy carriers and posttransfusion hepatitis. The prevalence of ay in the Bombay sample is in contrast to the predominance of ad reported from North India. These findings may suggest multifocal infection in different regions of India.

Carrier State↗
PubMed1977

A population genetic study of the Kota in the Nilgiri Hills, South India.

A population genetic study among the Kota of the Nilgiri Hills, South India, involved tests for abnormal haemoglobins, 5 red cell antigen systems, 4 serum protein and 13 red cell enzymes systems. Twelve systems are invariant in the Kota. The most distinctive characteristics are extremely low frequency of the A1 gene and complete absence of A2 in the ABO system, r(cde) in the Rh system, LDH cal-1 among the enzyme systems as well as absence of abnormal haemoglobins. A comparison of gene frequencies in those systems, which show variation, suggests that the Kota are more similar to the Toda than to any other tribal or caste population of the area. Genetic distance as well principal component analysis also reveals that the Toda and Kota are close to each other, in agreement with tradition.

Blood Group Antigens↗
PubMed1976

Population genetic studies in kerala and the nilgiris (South West India).

A total of nearly 1,000 persons belonging to a number of caste, religious and tribal groupings in Kerala and the Nilgiri Hills of South India have been tested for genetic variation in 4 blood group, 5 serum protein and 17 enzyme systems as well as haemoglobin. The distribution of blood groups, serum protein and enzyme groups is similar to that reported for other South Indian populations. Abnormal haemoglobins were detected in several populations. Abnormal haemoglobins were detected in several populations, HbS being present in more than 20% of the Irula and Kurumba in the Nilgiri Hills. In the Kerala populations there were 4 examples of Hb AD and 1 of Hb AE. Genetic distance estimates using the gene frequency data indicate that the closest groups are the Nayar and Izhava and the Brahmin and Nayar. The tribal populations are approximately twice as far from the Nayar as they are from the Izhava. The Todas of the Nilgiri Hills are somewhat closer to the Brahmin of Kerala than they are to the other tribal populations.

ABO Blood-Group System↗
PubMed1976

Genetic studies among the endogamous groups of Lohanas of North and West India.

Four groups of Lohanas, belonging to the Gujarati, Sindhi and Punjabi were studied for various genetic markers. Lohanas have higher B than A and low Rh(D) negative (1.65-4.64%). The Hp1 gene ranges from 0.1557 to 0.2639; Gm1 is lower (0.34-0.55) than in other populations in Southern India. G-6-PD deficiency was prevalent in 3-8%. All the four groups have a high incidence of the thalassaemia trait and possess Hb-D. Hb, J, and L were also observed in two groups. Data was analysed for intergroup differences.

ABO Blood-Group System↗
PubMed1976

Genetic studies among endogamous groups of Saraswats in Western India.

Three groups of Saraswat Brahmans in Western India and a group of Goan Catholics ethnologically related to Saraswats were studied for various genetic markers. Saraswats have higher A than B with an Rh(D)-negative incidence ranging from 10 to 17%. All the groups have low incidence of G-6-PD deficiency (up to 1%). Incidence of thalassaemia trait ranges from 1 to 6%. Gm(1) was present in 85-87%. Intergroup differences suggest genetic closeness between the various groups with genetic distance ranging from 0.8 to 1.5. Genetic relationship between Goan Catholics and Chitrapur Saraswats confirms the ethnological and historical evidence of relationship between the two groups.

ABO Blood-Group System↗