Suchergebnisse - "Mandal, Kausik"

PubPharm (158)

91

Molecular Testing of MECP2 Gene in Rett Syndrome Phenotypes in Indian Girls

enthalten in: Indian pediatrics | 2018

von Lallar, M. | Rai, A. | Srivastava, P. | +4

92

Molecular Testing of MECP2 Gene in Rett Syndrome Phenotypes in Indian Girls

enthalten in: Indian pediatrics | 2018

von Lallar, M. | Rai, A. | Srivastava, P. | +4

93

Molecular Testing of MECP2 Gene in Rett Syndrome Phenotypes in Indian Girls

enthalten in: Indian pediatrics | 2018

von Lallar, M. | Rai, A. | Srivastava, P. | +4

94

Study of the association of forkhead box P3 (FOXP3) gene polymorphisms with unexplained recurrent spontaneous abortions in Indian population

enthalten in: Journal of genetics | 2018

von Mishra, S. | Srivastava, A. | Mandal, K. | +1

95

Study of the association of forkhead box P3 (FOXP3) gene polymorphisms with unexplained recurrent spontaneous abortions in Indian population

enthalten in: Journal of genetics | 2018

von Mishra, S. | Srivastava, A. | Mandal, K. | +1

96

Next Generation Sequencing in Diagnosis of MLPA Negative Cases Presenting as Duchenne/ Becker Muscular Dystrophies

enthalten in: Indian journal of pediatrics | 2018

von Singh, B. | Mandal, K. | Lallar, M. | +4

97

Phenotypic characterization of derivative 22 syndrome : case series and review

enthalten in: Journal of genetics | 2018

von Saxena, D. | Srivastava, P. | Tuteja, M. | +2

98

Connexin 26 (GJB2) Mutations Associated with Non-Syndromic Hearing Loss (NSHL)

enthalten in: Indian journal of pediatrics | 2018

von Mishra, S. | Pandey, H. | Srivastava, P. | +2

99

Phenotypic characterization of derivative 22 syndrome: case series and review

enthalten in: Journal of genetics | 2018

von Saxena, D. | Srivastava, P. | Tuteja, M. | +2

100

Phenotypic characterization of derivative 22 syndrome: case series and review

enthalten in: Journal of genetics | 2018

von Saxena, D. | Srivastava, P. | Tuteja, M. | +2