Topic: Child
Journal: American Journal of Human Genetics
Documents
A list of abstracts that contain a topic of "Child" and a journal name of "American Journal of Human Genetics".
Loss-of-function Mutations in Euchromatin Histone Methyl Transferase 1 (Ehmt1) Cause the 9q34 Subtelomeric Deletion Syndrome.
PMID: 16826528
Genome Scan for Tourette Disorder in Affected-sibling-pair and Multigenerational Families.
PMID: 17304708
Clinical and Molecular Phenotype of Aicardi-goutieres Syndrome.
PMID: 17846997
A Common Haplotype of the Glucokinase Gene Alters Fasting Glucose and Birth Weight: Association in Six Studies and Population-genetics Analyses.
PMID: 17186458
Mutations in Cytokine Receptor-like Factor 1 (Crlf1) Account for Both Crisponi and Cold-induced Sweating Syndromes.
PMID: 17436251
Oligonucleotide Microarray Analysis of Genomic Imbalance in Children with Mental Retardation.
PMID: 16909388
Copy-number Variations Measured by Single-nucleotide-polymorphism Oligonucleotide Arrays in Patients with Mental Retardation.
PMID: 17847001
