Related Experiment Videos
A familial syndrome of deafness, alopecia, and hypogonadism
The Journal of Pediatrics
|March 1, 1973
Abstract
No abstract available in PubMed .
Related Concept Videos
Articles linked to this work by shared authors, journal, and citation graph.
Duane syndrome associated with features of the cat-eye syndrome and mosaicism for a supernumerary chromosome probably derived from number 22.
Journal of pediatric ophthalmology and strabismus·2014
Education and testing strategy for large-scale cystic fibrosis carrier screening.
Journal of genetic counseling·2013
Haplotypes at the DRD2 locus and severe alcoholism.
American journal of medical genetics·2000
A new locus for autosomal dominant cataract on chromosome 12q13.
Investigative ophthalmology & visual science·2000
Linkage analysis and loss of heterozygosity for chromosome arm 1p in familial breast cancer.
Genes, chromosomes & cancer·1999
Prenatal Exposure to Delta 9-Tetrahydrocannabinol and Child Neurodevelopment: A Critical Windows Analysis.
The Journal of pediatrics·2026
Decoding Parenting Style and Emotional Connection in Infants With Cerebral Palsy: A Prospective, Multicenter Study.
The Journal of pediatrics·2026
Delayed diagnosis of familial glucocorticoid deficiency type 4 in a child with epilepsy: a case report and literature review.
Journal of pediatric endocrinology & metabolism : JPEM·2026
[Low-frequency trisomy 21 mosaicism diagnosed following conflicting prenatal testing].
Ugeskrift for laeger·2026
Reduced insulin/IGF-1 signaling extends reproductive span through somatic gonadal collagen-mediated maintenance of oocyte and embryo quality in Caenorhabditis elegans.
Cell communication and signaling : CCS·2026