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The Journal of Clinical Endocrinology and Metabolism|June 16, 2005
Androgen receptor CAGn repeat length influences phenotype of 47,XXY (Klinefelter) syndromeAndrew R Zinn, Purita Ramos, Frederick F Elder, et al.
The Journal of Pediatrics|April 16, 2008
Effect of ascertainment and genetic features on the phenotype of Klinefelter syndromeMartha P D Zeger, Andrew R Zinn, Najiba Lahlou, et al.
Behavioral and Brain Functions : BBF|May 23, 2007
A Turner syndrome neurocognitive phenotype maps to Xp22.3Andrew R Zinn, David Roeltgen, Gerry Stefanatos, et al.
American Journal of Medical Genetics. Part A|February 13, 2008
Cognitive and motor development during childhood in boys with Klinefelter syndromeJudith L Ross, David P Roeltgen, Gerry Stefanatos, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|October 24, 2007
EFHC2 SNP rs7055196 is not associated with fear recognition in 45,X Turner syndromeAndrew R Zinn, Harvey Kushner, Judith L Ross
American Journal of Medical Genetics. Part A|December 12, 2002
Mesomelic and rhizomelic short stature: The phenotype of combined Leri-Weill dyschondrosteosis and achondroplasia or hypochondroplasiaJudith L Ross, Gary Bellus, Charles I Scott, et al.
American Journal of Medical Genetics. Part A|March 31, 2007
Compound heterozygosity of SHOX-encompassing and downstream PAR1 deletions results in Langer mesomelic dysplasia (LMD)Angel Campos-Barros, Sara Benito-Sanz, Judith L Ross, et al.
Developmental Disabilities Research Reviews|December 17, 2009
An extra X or Y chromosome: contrasting the cognitive and motor phenotypes in childhood in boys with 47,XYY syndrome or 47,XXY Klinefelter syndromeJudith L Ross, Martha P D Zeger, Harvey Kushner, et al.
American Journal of Medical Genetics|July 13, 2002
Complete SHOX deficiency causes Langer mesomelic dysplasiaAndrew R Zinn, Fanglin Wei, Ling Zhang, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|June 5, 2019
Y chromosome gene copy number and lack of autism phenotype in a male with an isodicentric Y chromosome and absent NLGN4Y expressionJudith L Ross, Luke Bloy, Timothy P L Roberts, et al.
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