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One or more keywords matched the following items that are connected to Zinn, Andrew
Item TypeName
Concept Chromosome Aberrations
Concept Chromosome Deletion
Concept Chromosome Mapping
Concept Chromosomes, Human, Pair 22
Concept Chromosomes, Human, Pair 9
Concept Chromosomes, Human, X
Concept Chromosomes, Human, Y
Concept X Chromosome Inactivation
Concept Chromosome Breakpoints
Academic Article The physical phenotype of girls and women with Turner syndrome is not X-imprinted.
Academic Article Maternal X chromosome, visceral adiposity, and lipid profile.
Academic Article Cognition and the sex chromosomes: studies in Turner syndrome.
Academic Article Cryptic chromosomal abnormalities identified in children with congenital heart disease.
Academic Article EFHC2 SNP rs7055196 is not associated with fear recognition in 45,X Turner syndrome.
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 Submicroscopic chromosomal copy number variations identified in children with hypoplastic left heart syndrome.
Academic Article Compound heterozygosity of SHOX-encompassing and downstream PAR1 deletions results in Langer mesomelic dysplasia (LMD).
Academic Article Phenotypic expansion of the supernumerary derivative (22) chromosome syndrome: VACTERL and Hirschsprung's disease.
Academic Article Increased prevalence of ADHD in Turner syndrome with no evidence of imprinting effects.
Academic Article Androgen receptor CAGn repeat length influences phenotype of 47,XXY (Klinefelter) syndrome.
Academic Article Refined mapping of X-linked reticulate pigmentary disorder and sequencing of candidate genes.
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.
Academic Article Sex-chromosome dosage effects on gene expression in humans.
Academic Article UBE2A deficiency syndrome: Mild to severe intellectual disability accompanied by seizures, absent speech, urogenital, and skin anomalies in male patients.
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  • Chromosomes