Thomas Jefferson University

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Zinn, Andrew
One or more keywords matched the following items that are connected to Zinn, Andrew
Item TypeName
Concept Phenotype
Academic Article Mesomelic and rhizomelic short stature: The phenotype of combined Leri-Weill dyschondrosteosis and achondroplasia or hypochondroplasia.
Academic Article A Turner syndrome neurocognitive phenotype maps to Xp22.3.
Academic Article The physical phenotype of girls and women with Turner syndrome is not X-imprinted.
Academic Article An extra X or Y chromosome: contrasting the cognitive and motor phenotypes in childhood in boys with 47,XYY syndrome or 47,XXY Klinefelter syndrome.
Academic Article Effect of ascertainment and genetic features on the phenotype of Klinefelter syndrome.
Academic Article The phenotype of short stature homeobox gene (SHOX) deficiency in childhood: contrasting children with Leri-Weill dyschondrosteosis and Turner syndrome.
Academic Article Behavioral and social phenotypes in boys with 47,XYY syndrome or 47,XXY Klinefelter syndrome.
Academic Article Phenotypic expansion of the supernumerary derivative (22) chromosome syndrome: VACTERL and Hirschsprung's disease.
Academic Article Androgen receptor CAGn repeat length influences phenotype of 47,XXY (Klinefelter) syndrome.
Academic Article Screening and familial characterization of copy-number variations in NR5A1 in 46,XY disorders of sex development and premature ovarian failure.
Academic Article Y chromosome gene copy number and lack of autism phenotype in a male with an isodicentric Y chromosome and absent NLGN4Y expression.
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