R. Mathur

Molecular Characterization of Mutations in Indian Children with Congenital Adrenal Hyperplasia due to Steroid 21-Hydroxylase Deficiency

M. Kabra, P. Menon, I. Verma, 2001, Journal of pediatric endocrinology & metabolism : JPEM.

Cytogenetic causes for recurrent spontaneous abortions - An experience of 742 couples (1484 cases)

M. Kabra, P. Menon, I. Verma, 2005 .

Detection of complex chromosomal rearrangements in a woman with repeated spontaneous abortions

M. Kabra, S. Dubey, R. Mathur, 2001, Acta obstetricia et gynecologica Scandinavica.

Prenatal diagnosis and treatment of steroid 21-hydroxylase deficiency (congenital adrenal hyperplasia)

M. Kabra, R. Mathur, 2000, Indian journal of pediatrics.

Rapid prenatal karyotyping using foetal blood obtained by cordocentesis.

M. Kabra, A. Kriplani, D. Deka, 2002, The National medical journal of India.

Recent advances in chromosome breakage syndromes and their diagnosis.

M. R. Chowdhury, R. Mathur, G. Singh, 2000, Indian pediatrics.

Utility of XY-amelogenin gene primers for detection of sex chromosomes.

I. Verma, R. Mathur, M. Chowdhury, 1998, The Indian journal of medical research.