This page shows the details of why an item matched the keywords from your search.
One or more keywords matched the following items that are connected to
Zinn, Andrew
Item Type | Name |
Concept
|
Chromosomes, Human, Pair 22
|
Concept
|
Chromosomes, Human, Pair 9
|
Concept
|
Chromosomes, Human, X
|
Concept
|
Chromosomes, Human, Y
|
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
|
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
|
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
|
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.
|