Suchergebnisse - "Jamwal, Manu"

PubPharm (74)

61

Homozygous KLF1 mutation c.901C>T (p.Arg301Cys) resulting in mild thalassemia intermedia in an Indian : A next-generation sequencing diagnosis

enthalten in: Blood cells, molecules & diseases | 2018

von Rani, N. | Jamwal, M. | Kaur, J. | +5

62

Coagulation F13A1 V34L, fibrinogen and homocysteine versus conventional risk factors in the pathogenesis of MI in young persons

enthalten in: Acta cardiologica | 2018

von Vishwajeet, V. | Jamwal, M. | Sharma, P. | +4

63

Overhydrated stomatocytosis associated with a complex RHAG genotype including a novel de novo mutation

enthalten in: Journal of clinical pathology | 2018

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

64

Optimal Reference Gene Selection for Expression Studies in Human Reticulocytes

enthalten in: The Journal of molecular diagnostics : JMD | 2018

von Aggarwal, A. | Jamwal, M. | Viswanathan, G. | +5

65

First report of Mediterranean stomatocytosis/macrothrombocytopenia in an Indian family : a diagnostic dilemma

enthalten in: Pathology | 2017

von Jamwal, M. | Aggarwal, A. | Maitra, A. | +6

66

Next-generation sequencing unravels homozygous mutation in glucose-6-phosphate isomerase, GPIc.1040G>A (p.Arg347His) causing hemolysis in an Indian infant

enthalten in: Clinica chimica acta; international journal of clinical chemistry | 2017

von Jamwal, M. | Aggarwal, A. | Das, A. | +6

67

Next-generation sequencing unravels homozygous mutation in glucose-6-phosphate isomerase, GPIc.1040G>A (p.Arg347His) causing hemolysis in an Indian infant

enthalten in: Clinica chimica acta | 2017

von Jamwal, M. | Aggarwal, A. | Das, A. | +6

68

Next-generation sequencing unravels homozygous mutation in glucose-6-phosphate isomerase, GPIc.1040G>A (p.Arg347His) causing hemolysis in an Indian infant

enthalten in: Clinica chimica acta | 2017

von Jamwal, M. | Aggarwal, A. | Das, A. | +6

69

First report of Mediterranean stomatocytosis/macrothrombocytopenia in an Indian family: a diagnostic dilemma

enthalten in: Pathology | 2017

von Jamwal, M. | Aggarwal, A. | Maitra, A. | +6

70

Disease-modifying influences of coexistent G6PD-deficiency, Gilbert syndrome and deletional alpha thalassemia in hereditary spherocytosis : A report of three cases

enthalten in: Clinica chimica acta; international journal of clinical chemistry | 2016

von Jamwal, M. | Aggarwal, A. | Kumar, V. | +5