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One or more keywords matched the following items that are connected to
Zinn, Andrew
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Concept
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Chromosome Aberrations
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Concept
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Chromosome Deletion
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Concept
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Chromosome Mapping
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Concept
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Chromosomes, Human, Pair 22
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Concept
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Chromosomes, Human, Pair 9
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Concept
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X Chromosome Inactivation
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Concept
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Chromosome Breakpoints
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Academic Article
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Maternal X chromosome, visceral adiposity, and lipid profile.
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Academic Article
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Cognition and the sex chromosomes: studies in Turner syndrome.
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Academic Article
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Cryptic chromosomal abnormalities identified in children with congenital heart disease.
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Academic Article
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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.
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Academic Article
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Submicroscopic chromosomal copy number variations identified in children with hypoplastic left heart syndrome.
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Academic Article
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Compound heterozygosity of SHOX-encompassing and downstream PAR1 deletions results in Langer mesomelic dysplasia (LMD).
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Academic Article
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Phenotypic expansion of the supernumerary derivative (22) chromosome syndrome: VACTERL and Hirschsprung's disease.
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Academic Article
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Androgen receptor CAGn repeat length influences phenotype of 47,XXY (Klinefelter) syndrome.
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Academic Article
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Refined mapping of X-linked reticulate pigmentary disorder and sequencing of candidate genes.
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Academic Article
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Screening and familial characterization of copy-number variations in NR5A1 in 46,XY disorders of sex development and premature ovarian failure.
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Academic Article
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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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Academic Article
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Sex-chromosome dosage effects on gene expression in humans.
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