Kavita A. Khatod

Pune, MH, India

Last Updated: 09/26/2026

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Found 9 publications

Clinical application of a novel next generation sequencing assay for CYP21A2 gene in 310 cases of 21- hydroxylase congenital adrenal hyperplasia from India.

Clinical application of a novel next generation sequencing assay for CYP21A2 gene in 310 cases of 21- hydroxylase congenital adrenal hyperplasia from India.

Journal: Endocrine

Published: May 02, 2020

Use of two complementary new molecular techniques, next-generation sequencing and droplet digital PCR, for diagnosis of an F8 gene deletion and subsequent carrier analysis in a family with haemophilia A: A Case Report.

Use of two complementary new molecular techniques, next-generation sequencing and droplet digital PCR, for diagnosis of an F8 gene deletion and subsequent carrier analysis in a family with haemophilia A: A Case Report.

Journal: Haemophilia : the official journal of the World Federation of Hemophilia

Published: May 08, 2018

Association of Fat Mass and Obesity-associated Gene Variant with Lifestyle Factors and Body Fat in Indian Children.

Association of Fat Mass and Obesity-associated Gene Variant with Lifestyle Factors and Body Fat in Indian Children.

Journal: Indian journal of endocrinology and metabolism

Published: May 02, 2017

Molecular genetics of growth hormone deficient children: correlation with auxology and response to first year of growth hormone therapy.

Molecular genetics of growth hormone deficient children: correlation with auxology and response to first year of growth hormone therapy.

Journal: Journal of pediatric endocrinology & metabolism : JPEM

Published: September 28, 2016

Influence of Vitamin D Receptor Gene Fok1 Polymorphism on Bone Mass Accrual Post Calcium and Vitamin D Supplementation.

Influence of Vitamin D Receptor Gene Fok1 Polymorphism on Bone Mass Accrual Post Calcium and Vitamin D Supplementation.

Journal: Indian journal of pediatrics

Published: December 15, 2014

Molecular characterization in a case of isolated growth hormone deficiency and further prenatal diagnosis of an unborn sibling.

Molecular characterization in a case of isolated growth hormone deficiency and further prenatal diagnosis of an unborn sibling.

Journal: Indian journal of human genetics

Published: February 06, 2014

Clinical applicability of rapid detection of SRY and DYS14 genes in patients with disorders of sex development using an indigenously developed 5' exonuclease based assay.

Clinical applicability of rapid detection of SRY and DYS14 genes in patients with disorders of sex development using an indigenously developed 5' exonuclease based assay.

Journal: Journal of pediatric endocrinology & metabolism : JPEM

Published: October 27, 2013

Detection of carrier status and mutations in family members of a child with complete deletion of the DAX1 gene using multiplex ligation-dependent probe amplification.

Detection of carrier status and mutations in family members of a child with complete deletion of the DAX1 gene using multiplex ligation-dependent probe amplification.

Journal: Indian journal of pediatrics

Published: March 11, 2013

Entire DAX1 gene deletion in an Indian boy with adrenal hypoplasia congenita.

Entire DAX1 gene deletion in an Indian boy with adrenal hypoplasia congenita.

Journal: Indian journal of pediatrics

Published: April 28, 2012

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Last Updated: 09/26/2026