K. Khatod

发表

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

A. Khadilkar, V. Khadilkar, V. Ekbote, 2017, Journal of pediatric endocrinology & metabolism : JPEM.

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

S. Chiplonkar, A. Khadilkar, V. Khadilkar, 2017, Indian journal of endocrinology and metabolism.

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

S. Chiplonkar, N. Sanwalka, A. Khadilkar, 2015, The Indian Journal of Pediatrics.

Vitamin D receptor gene polymorphisms and bone mass indices in post-menarchal Indian adolescent girls

S. Chiplonkar, N. Sanwalka, A. Khadilkar, 2012, Journal of Bone and Mineral Metabolism.

HBB gene mutation spectrum in an Indian cohort of 1530 cases using an in-house targeted next-generation sequencing assay

V. Ramanan, P. Majethia, Priyanka V. Gangodkar, 2020, Journal of Hematopathology.

Allele-Specific Binding of CTCF to the Multipartite Imprinting Control Region KvDMR1

Victor V Lobanenkov, Jong-Yeon Shin, E. Pugacheva, 2007, Molecular and Cellular Biology.

Silencing of CDKN1C (p57KIP2) is associated with hypomethylation at KvDMR1 in Beckwith–Wiedemann syndrome

C. Junien, W. Reik, V. D. Der Kaloustian, 2003, Journal of medical genetics.

Silencing of CDKN 1 C ( p 57 KIP 2 ) is associated with hypomethylation at KvDMR 1 in Beckwith – Wiedemann syndrome

C. Junien, W. Reik, E. Maher, 2003 .

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

K. Ganesan, N. Gupta, D. Dayal, 2020, Endocrine.

Silencing of CDKN1C ( p57 KIP2 ) is associated with hypomethylation at KvDMR1 in Beckwith–Wiedemann syndrome

C. Junien, W. Reik, N. Diaz-Meyer, 2003 .

Targeted NGS analysis of the canonical genes in 274 Indian patients with suspected myeloproliferative neoplasms: An Indian diagnostic laboratory’s perspective

Priyanka V. Gangodkar, Vijay Ramanan, M. Agarwal, 2022, Indian Journal of Pathology and Oncology.

Entire DAX1 Gene Deletion in an Indian Boy with Adrenal Hypoplasia Congenita

A. Khadilkar, V. Khadilkar, R. Jahagirdar, 2013, The Indian Journal of Pediatrics.

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

A. Khadilkar, V. Khadilkar, C. Datar, 2013, Indian journal of human genetics.

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

Priyanka V. Gangodkar, M. Agarwal, Siddharth Anand, 2018, Haemophilia : the official journal of the World Federation of Hemophilia.