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Jinrui Idengaku Zasshi. the Japanese Journal of Human Genetics
|
September 1, 1991
Unilateral gonadal dysgenesis with both testis and fallopian tube on the same side in a 45,X/46,X inv (Y) mosaic male
U Radhakrishna, V C Shah, N J Chinoy
Cytogenetic and Genome Research
|
November 20, 2002
Search for the second Peutz-Jeghers syndrome locus: exclusion of the STK13, PRKCG, KLK10, and PSCD2 genes on chromosome 19 and the STK11IP gene on chromosome 2
K Buchet-Poyau, H Mehenni, U Radhakrishna, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology
|
April 13, 2019
Placental DNA methylation changes in detection of tetralogy of Fallot
R Bahado-Singh, S Vishweswaraiah, N K Mishra, et al.
American Journal of Medical Genetics
|
December 11, 1996
An autosomal dominant triphalangeal thumb: polysyndactyly syndrome with variable expression in a large Indian family maps to 7q36
U Radhakrishna, J L Blouin, J V Solanki, et al.
Annales De Genetique
|
January 1, 1991
A triple-X female with long arm deletion of one of the X-chromosomes associated with primary amenorrhoea: 47,XX, +del(X) (q27.3)
U Radhakrishna, V C Shah, H N Highland, et al.
Annales De Genetique
|
January 1, 1992
Translocation t(22;22)(p11.1;q11.1) and NOR studies in a female with a history of repeated fetal loss
A S Multani, U Radhakrishna, F J Sheth, et al.
Journal of Medical Genetics
|
April 1, 1993
Polydactyly: a study of a five generation Indian family
U Radhakrishna, A S Multani, J V Solanki, et al.
Urologia Internationalis
|
January 1, 1996
Incomplete gonadal dysgenesis
F J Sheth, A S Multani, J J Sheth, et al.
European Journal of Human Genetics : EJHG
|
February 15, 2001
An apparently dominant bipolar affective disorder (BPAD) locus on chromosome 20p11.2-q11.2 in a large Turkish pedigree
U Radhakrishna, S Senol, H Herken, et al.
American Journal of Human Genetics
|
March 1, 1997
Mapping one form of autosomal dominant postaxial polydactyly type A to chromosome 7p15-q11.23 by linkage analysis
U Radhakrishna, J L Blouin, H Mehenni, et al.
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Search research articles
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Showing results (1-10 of 23) with videos related to
Sort By:
Page
of 3
Jinrui Idengaku Zasshi. the Japanese Journal of Human Genetics
|
September 1, 1991
Unilateral gonadal dysgenesis with both testis and fallopian tube on the same side in a 45,X/46,X inv (Y) mosaic male
U Radhakrishna, V C Shah, N J Chinoy
Cytogenetic and Genome Research
|
November 20, 2002
Search for the second Peutz-Jeghers syndrome locus: exclusion of the STK13, PRKCG, KLK10, and PSCD2 genes on chromosome 19 and the STK11IP gene on chromosome 2
K Buchet-Poyau, H Mehenni, U Radhakrishna, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology
|
April 13, 2019
Placental DNA methylation changes in detection of tetralogy of Fallot
R Bahado-Singh, S Vishweswaraiah, N K Mishra, et al.
American Journal of Medical Genetics
|
December 11, 1996
An autosomal dominant triphalangeal thumb: polysyndactyly syndrome with variable expression in a large Indian family maps to 7q36
U Radhakrishna, J L Blouin, J V Solanki, et al.
Annales De Genetique
|
January 1, 1991
A triple-X female with long arm deletion of one of the X-chromosomes associated with primary amenorrhoea: 47,XX, +del(X) (q27.3)
U Radhakrishna, V C Shah, H N Highland, et al.
Annales De Genetique
|
January 1, 1992
Translocation t(22;22)(p11.1;q11.1) and NOR studies in a female with a history of repeated fetal loss
A S Multani, U Radhakrishna, F J Sheth, et al.
Journal of Medical Genetics
|
April 1, 1993
Polydactyly: a study of a five generation Indian family
U Radhakrishna, A S Multani, J V Solanki, et al.
Urologia Internationalis
|
January 1, 1996
Incomplete gonadal dysgenesis
F J Sheth, A S Multani, J J Sheth, et al.
European Journal of Human Genetics : EJHG
|
February 15, 2001
An apparently dominant bipolar affective disorder (BPAD) locus on chromosome 20p11.2-q11.2 in a large Turkish pedigree
U Radhakrishna, S Senol, H Herken, et al.
American Journal of Human Genetics
|
March 1, 1997
Mapping one form of autosomal dominant postaxial polydactyly type A to chromosome 7p15-q11.23 by linkage analysis
U Radhakrishna, J L Blouin, H Mehenni, et al.
Page
of 3