Related Experiment Videos
Detection of Y-specific sequences in patients with Turner syndrome
American Journal of Medical Genetics
|October 26, 2002
Abstract
No abstract available in PubMed .
Related Concept Videos
Articles linked to this work by shared authors, journal, and citation graph.
Common data elements for arthrogryposis multiplex congenita: An international framework.
Developmental medicine and child neurology·2024
Personal journeys to and in human genetics and dysmorphology.
American journal of medical genetics. Part A·2024
Perspectives on the future of dysmorphology.
American journal of medical genetics. Part A·2022
Lethal respiratory course and additional features expand the phenotypic spectrum of PIEZO2-related distal arthrogryposis type 5.
American journal of medical genetics. Part A·2022
Examining the Vanishing Twin Hypothesis of Neural Tube Defects: Application of an Epigenetic Predictor for Monozygotic Twinning.
Twin research and human genetics : the official journal of the International Society for Twin Studies·2021
The contributions of careful clinical observations: A legacy.
American journal of medical genetics. Part A·2021
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
A catalytically competent sperm PLCzeta variant causes fertilization failure through protein insufficiency.
Journal of assisted reproduction and genetics·2026
Mass Spectrometry in Authentication and Forensic Approaches for Determining the Origin of Hazardous Chemicals.
Mass spectrometry reviews·2026