Related Experiment Videos
Dysgenetic male pseudohermaphroditism in a 45,X/46,X,del(Y)(q11.1) mosaic infant
American Journal of Medical Genetics
|March 1, 1987
Abstract:
We describe an infant with dysgenetic male pseudohermaphroditism and the karyotype 45,X/46,X,del(Y)(q11.1). Histologic examination of the resected gonads showed cortical dysplasia indicative of incipient gonadoblastoma.
Related Concept Videos
Articles linked to this work by shared authors, journal, and citation graph.
Redefining the risks of prenatally ascertained supernumerary marker chromosomes: a collaborative study.
Journal of medical genetics·2006
Prenatal diagnosis of 22q11.2 deletion when ultrasound examination reveals a heart defect.
Genetics in medicine : official journal of the American College of Medical Genetics·2001
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
Age-related variation in oxygen transport but stable mixed venous oxygen saturation in anaesthetised children.
European journal of anaesthesiology·2026
Remote Patient Monitoring for Neonates Discharged Home on Nasogastric Tube Feeds: A Multicenter Survey of Practices, Eligibility Criteria, and Implementation Barriers.
Telemedicine journal and e-health : the official journal of the American Telemedicine Association·2026