Search research articles
Contact Us
Filters
Showing results (11-20 of 30) with videos related to
Page
of 3
Sort By:
Genes, Chromosomes & Cancer
|
May 1, 1994
Malignant rhabdoid tumor of the kidney: involvement of chromosome 22
V Shashi, M A Lovell, C von Kap-herr, et al.
Journal of Intellectual Disability Research : JIDR
|
June 8, 2013
Association of the family environment with behavioural and cognitive outcomes in children with chromosome 22q11.2 deletion syndrome
T M Allen, J Hersh, K Schoch, et al.
Clinical Genetics
|
September 17, 2003
Ring chromosome 17: phenotype variation by deletion size
V Shashi, J R White, M J Pettenati, et al.
Journal of Intellectual Disability Research : JIDR
|
September 3, 2011
Social skills and associated psychopathology in children with chromosome 22q11.2 deletion syndrome: implications for interventions
V Shashi, A Veerapandiyan, K Schoch, et al.
American Journal of Human Genetics
|
March 21, 2000
A unique form of mental retardation with a distinctive phenotype maps to Xq26-q27
V Shashi, M N Berry, S Shoaf, et al.
Journal of Natural Science, Biology, and Medicine
|
March 27, 2015
Awareness and practice concerning oral cancer among Ayurveda and Homeopathy practitioners in Davangere District: A speciality-wise analysis
Ravikumar S Kulkarni, P Dupare Arun, Raj Rai, et al.
Gynecologic Oncology
|
December 1, 1994
Interphase fluorescence in situ hybridization for trisomy 12 on archival ovarian sex cord-stromal tumors
V Shashi, W L Golden, C von Kap-Herr, et al.
American Journal of Human Genetics
|
June 1, 1996
Molecular analysis of recombination in a family with Duchenne muscular dystrophy and a large pericentric X chromosome inversion
V Shashi, W L Golden, P S Allinson, et al.
Journal of Intellectual Disability Research : JIDR
|
July 26, 2014
A tale worth telling: the impact of the diagnosis experience on disclosure of genetic disorders
J Goodwin, K Schoch, V Shashi, et al.
Clinical Genetics
|
March 18, 2006
Cognitive correlates of a functional COMT polymorphism in children with 22q11.2 deletion syndrome
V Shashi, M S Keshavan, T D Howard, et al.
Page
of 3
Search research articles
Search
Showing results (11-20 of 30) with videos related to
Sort By:
Page
of 3
Genes, Chromosomes & Cancer
|
May 1, 1994
Malignant rhabdoid tumor of the kidney: involvement of chromosome 22
V Shashi, M A Lovell, C von Kap-herr, et al.
Journal of Intellectual Disability Research : JIDR
|
June 8, 2013
Association of the family environment with behavioural and cognitive outcomes in children with chromosome 22q11.2 deletion syndrome
T M Allen, J Hersh, K Schoch, et al.
Clinical Genetics
|
September 17, 2003
Ring chromosome 17: phenotype variation by deletion size
V Shashi, J R White, M J Pettenati, et al.
Journal of Intellectual Disability Research : JIDR
|
September 3, 2011
Social skills and associated psychopathology in children with chromosome 22q11.2 deletion syndrome: implications for interventions
V Shashi, A Veerapandiyan, K Schoch, et al.
American Journal of Human Genetics
|
March 21, 2000
A unique form of mental retardation with a distinctive phenotype maps to Xq26-q27
V Shashi, M N Berry, S Shoaf, et al.
Journal of Natural Science, Biology, and Medicine
|
March 27, 2015
Awareness and practice concerning oral cancer among Ayurveda and Homeopathy practitioners in Davangere District: A speciality-wise analysis
Ravikumar S Kulkarni, P Dupare Arun, Raj Rai, et al.
Gynecologic Oncology
|
December 1, 1994
Interphase fluorescence in situ hybridization for trisomy 12 on archival ovarian sex cord-stromal tumors
V Shashi, W L Golden, C von Kap-Herr, et al.
American Journal of Human Genetics
|
June 1, 1996
Molecular analysis of recombination in a family with Duchenne muscular dystrophy and a large pericentric X chromosome inversion
V Shashi, W L Golden, P S Allinson, et al.
Journal of Intellectual Disability Research : JIDR
|
July 26, 2014
A tale worth telling: the impact of the diagnosis experience on disclosure of genetic disorders
J Goodwin, K Schoch, V Shashi, et al.
Clinical Genetics
|
March 18, 2006
Cognitive correlates of a functional COMT polymorphism in children with 22q11.2 deletion syndrome
V Shashi, M S Keshavan, T D Howard, et al.
Page
of 3