Related Experiment Videos
Craniosynostosis in the Ullrich-Turner syndrome
American Journal of Medical Genetics
|August 1, 1991
Abstract
No abstract available in PubMed .
Related Concept Videos
Articles linked to this work by shared authors, journal, and citation graph.
Trend in body mass index during childhood in 460 girls with idiopathic central precocious puberty.
Endocrine connections·2025
Etiology, histology, and long-term outcome of bilateral testicular regression: a large Belgian series.
Human reproduction open·2024
Primary ovarian insufficiency in RMND1 mitochondrial disease.
Mitochondrion·2022
[Nephrogenic syndrome of inappropriate antidiuresis: Early diagnosis avoids severe hyponatremia complications].
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie·2017
Hearing loss is part of the clinical picture of ENPP1 loss of function mutation.
Hormone research in paediatrics·2013
Defects of blastogenesis.
American journal of medical genetics·2002
Malformations of the craniofacial region: evolutionary, embryonic, genetic, and clinical perspectives.
American journal of medical genetics·2002
Limb anomalies: Developmental and evolutionary aspects.
American journal of medical genetics·2002
Molecular etiology of gut malformations and diseases.
American journal of medical genetics·2002
Ectodermal dysplasia with acanthosis nigricans (Lelis syndrome).
American journal of medical genetics·2002
Three cases of tetrasomy 9p.
American journal of medical genetics·2002
Clinical, Genetic, and Endocrine Features of Bardet-Biedl Syndrome in a Pediatric and Adult Cohort.
American journal of medical genetics. Part A·2026
Cross-trait genetic analysis maps shared polygenic architecture between primary aldosteronism and blood pressure to adrenal cell states.
Journal of translational medicine·2026
Genetic Variation in ADHD-Related Risk Genes in an Indigenous Population of the Amazon.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics·2026