V C SHAH
Overview
Explore the profile of V C SHAH including associated specialties, affiliations and a list of published articles.
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76
Citations
53
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Recent Articles
1.
Multani A, Sheth F, SHAH V, Chinoy N, Pathak S
Early Hum Dev
. 1996 Jul;
45(3):229-33.
PMID: 8855396
The Harlequin fetus is a distinct genetic entity with a strikingly grotesque appearance. Three siblings (two males, one female) with Harlequin Ichthyosis, a rare form of congenital disorder, born to...
2.
3.
SHAH V, Smart V
Cell Biol Int
. 1996 Jan;
20(1):3-6.
PMID: 8936401
The precise location of the SRY gene on the human Y chromosome has been revealed through studies of sex reversal cases involving deletion, cross-linking and mutations of the SRY gene....
4.
Sheth F, Multani A, Sheth J, Radhakrishna U, SHAH V, Chinoy N
Urol Int
. 1996 Jan;
56(1):57-60.
PMID: 8903559
A 21-year-old phenotypic male with ambiguous external genitalia and hypospadias was referred for cytogenetic studies. Exploratory laparotomy revealed presence of a small atropic uterus, unilateral gonadal dysgenesis with fallopian tubes...
5.
Sheth F, Multani A, SHAH V, Chinoy N
Indian J Pediatr
. 1995 May;
62(3):369-72.
PMID: 10829893
No abstract available.
6.
Sheth F, Radhakrishna U, Multani A, SHAH V, Chinoy N
Indian J Pediatr
. 1994 Mar;
61(2):189-92.
PMID: 7927618
No abstract available.
7.
Sane A, Chokshi S, Mishra V, Barad D, SHAH V, Nagpal S
Panminerva Med
. 1993 Sep;
35(3):131-3.
PMID: 8090526
In continuation of our studies on stress situations in female reproductive life span, serum lipid peroxide levels in terms of malondialdehyde (nmol/ml) have been determined in females [(n = 40)...
8.
Radhakrishna U, Multani A, Solanki J, SHAH V, Chinoy N
J Med Genet
. 1993 Apr;
30(4):296-9.
PMID: 8487274
Preaxial polydactyly was observed in up to five generations of an Indian family living in a village in the Rajkot district (Gujarat). Among the 71 affected members, 45 were males...
9.
Multani A, Radhakrishna U, Sheth F, SHAH V, Chinoy N
Ann Genet
. 1992 Jan;
35(2):105-9.
PMID: 1524406
A 32-year-old phenotypic female with a history of nine consecutive abortions each in the first trimester was referred for cytogenetic studies. She was found to have 45,XX,t(22;22) (p11.1;q11.1) chromosomal pattern....
10.
Radhakrishna U, SHAH V, Chinoy N
Jinrui Idengaku Zasshi
. 1991 Sep;
36(3):251-5.
PMID: 1753438
A 5-year-old male with ambiguous external genitalia, hypospadias and microphallus without an urethral orifice was referred for cytogenetic studies. Exploratory laparotomy revealed presence of an infantile uterus and unilateral gonadal...