Suchergebnisse - "Jamwal, Manu"

PubPharm (74)

51

Deciphering molecular heterogeneity of Indian families with hereditary spherocytosis using targeted next-generation sequencing : First South Asian study

enthalten in: British journal of haematology | 2020

von Aggarwal, A. | Jamwal, M. | Sharma, P. | +4

CommentIn: Int J Lab Hematol. 2021 Oct;43(5):e242-e243. - PMID 33470548

52

Phenotypic and genetic heterogeneity arising from a novel substitution at amino acid position Val205 in GATA1 related X-linked thrombocytopenia with dyserythropoietic anemia

enthalten in: Blood cells, molecules & diseases | 2020

von Jamwal, M. | Aggarwal, A. | Sharma, P. | +3

53

Laboratory Approach to Hemolytic Anemia

enthalten in: Indian journal of pediatrics | 2020

von Jamwal, M. | Sharma, P. | Das, R.

54

Deciphering molecular heterogeneity of Indian families with hereditary spherocytosis using targeted next‐generation sequencing : First South Asian study

enthalten in: British Journal of Haematology | 2020

von Aggarwal, A. | Jamwal, M. | Sharma, P. | +4

55

Laboratory Approach to Hemolytic Anemia

enthalten in: Indian journal of pediatrics | 2019

von Jamwal, M. | Sharma, P. | Das, R.

56

A novel germline RUNX1 mutation with co-occurrence of somatic alterations in a case of myeloid neoplasm with familial thrombocytopenia : first report from India

enthalten in: Leukemia & lymphoma | 2019

von Rajpal, S. | Jain, A. | Jamwal, M. | +5

57

A nonsense variant in the Hexokinase 1 gene (HK1) causing severe non-spherocytic haemolytic anaemia : genetic analysis exemplifies ambiguity due to multiple Isoforms

enthalten in: British journal of haematology | 2019

von Jamwal, M. | Aggarwal, A. | Palodi, A. | +4

58

First report of homocystinuria-megaloblastic anaemia, cobalamin E complementation type, in an Indian child

enthalten in: Pathology | 2019

von Jamwal, M. | Aggarwal, A. | Sharma, P. | +4

59

A nonsense variant in the Hexokinase 1 gene ( HK1) causing severe non‐spherocytic haemolytic anaemia : genetic analysis exemplifies ambiguity due to multiple Isoforms

enthalten in: British Journal of Haematology | 2019

von Jamwal, M. | Aggarwal, A. | Palodi, A. | +4

60

Adult onset hereditary hemochromatosis is associated with a novel recurrent Hemojuvelin (HJV) gene mutation in north Indians

enthalten in: Blood cells, molecules & diseases | 2018

von Dhillon, B. | Chopra, G. | Jamwal, M. | +6