Genetics of Parkinson's disease
Genetics and substance abuse
Genes and tobacco dependence
Searching for human genes involved in alcohol dependence
Intoxicating Genes
Developmental eye disease - a genome era paradigm
Genetic landmarks through philately - The Habsburg jaw
Associations of angiotensinogen gene mutations with hypertension and myocardial infarction in a gulf population
Pallister-Killian syndrome [i(12p)]: first pre-natal diagnosis using cordocentesis in the second trimester confirmed by in situ hybridization
Unusual clinical features in an Angelman syndrome patient with uniparental disomy due to a translocation 15q15q
An unusual fragile X sibship: female compound heterozygote and male with a partially methylated full mutation
Autosomal recessive familial exudative vitreoretinopathy: evidence for genetic heterogeneity
Mexican geneticists' opinions on disclosure issues
t(1;18)(q32.1;q22.1) associated with genitourinary malformations
Identification and characterization of a de novo partial trisomy 10p by comparative genomic hybridization (CGH)
Presence of the AZF region in a female with an idic(Y)(q11)
Autosomal dominant carpal tunnel syndrome
X-inactivation pattern in the liver of a manifesting female with ornithine transcarbamylase (OTC) deficiency
Molecular analysis of two pre-mutations in myotonic dystrophy
Failure to identify the ryanodine receptor G1021A mutation in a large North American population with malignant hyperthermia
Variants of B cell lymphoma 6 (BCL6) and marked atopy
Fragile X and Rett syndromes in Puerto Rico
Fragile X syndrome, mental retardation and macroorchidism
I1307K APC and hMLH1 mutations in a non-Jewish family with hereditary non-polyposis colorectal cancer
Two sisters with different chromosomal microdeletions: Rubinstein-Taybi syndrome and 22q deletion syndrome