Detalhe da pesquisa
1.
Mother-to-son transmission of a luteinizing hormone receptor activating mutation in a prepubertal child with testotoxicosis.
J Pediatr Endocrinol Metab
; 22(3): 275-9, 2009 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-19492585
2.
Molecular diagnosis of 5alpha-reductase-2 gene mutation in two Indian families with male pseudohermaphroditism.
Asian J Androl
; 10(5): 815-8, 2008 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-18097518
3.
Gender identity of children and young adults with 5alpha-reductase deficiency.
J Pediatr Endocrinol Metab
; 21(2): 173-9, 2008 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-18422030
4.
Apparent male gender identity in a patient with complete androgen insensitivity syndrome.
Arch Sex Behav
; 38(6): 873-5, 2009 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-19636694
5.
Prenatal treatment of mothers with fetuses at risk for congenital adrenal hyperplasia: How relevant is it to Indian context?
Indian J Endocrinol Metab
; 17(3): 373-5, 2013 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-23869292
6.
Pubertal development among girls with classical congenital adrenal hyperplasia initiated on treatment at different ages.
Indian J Endocrinol Metab
; 16(4): 599-603, 2012 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-22837923
7.
Phenotypical, biological, and molecular heterogeneity of 5α-reductase deficiency: an extensive international experience of 55 patients.
J Clin Endocrinol Metab
; 96(2): 296-307, 2011 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-21147889
8.
Genomics revolution on andrology: genetic testing for male infertility.
Asian J Androl
; 12(3): 449-50, 2010 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-20436514
9.
Mutations within the transcription factor PROP1 are rare in a cohort of patients with sporadic combined pituitary hormone deficiency (CPHD).
Clin Endocrinol (Oxf)
; 63(1): 10-8, 2005 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-15963055