Related Experiment Videos
[The late forms of retinoblastoma: a snare for genetic counseling]
Abstract
No abstract available in PubMed .
Related Concept Videos
Articles linked to this work by shared authors, journal, and citation graph.
Prader-Willi syndrome and polygonosomal abnormalities in males:about a Prader-Willi/47,XYY patient.
Annales de genetique·2001
A new mutation in the six-domain of SIX3 gene causes holoprosencephaly.
European journal of human genetics : EJHG·2000
Gastric carcinoma in Sotos syndrome (cerebral gigantism).
Annales de genetique·1999
Unusual fan shaped ossification in a female fetus with radiological features of boomerang dysplasia.
Journal of medical genetics·1999
High prevalence of cervical intra-epithelial neoplasia in women treated for pelvic inflammatory disease.
European journal of obstetrics, gynecology, and reproductive biology·1998
[Ultrasonic prenatal diagnosis of the Jarcho-Levin syndrome].
Journal de genetique humaine·1989
[Genetic mapping of chromosome X: known localizations].
Journal de genetique humaine·1989
[Animal models of gene therapy].
Journal de genetique humaine·1989
[Frontonasal dysplasia or the median cleft face syndrome: a case report].
Journal de genetique humaine·1989
[Linkage disequilibrium and DNA markers associated with the gene for cystic fibrosis].
Journal de genetique humaine·1989
[F.G. syndrome: a rare and/or extremely polymorphic syndrome?].
Journal de genetique humaine·1989
Caregiver's perspectives toward genome sequencing in children with neurodevelopmental disorders: Integrating genomic information into pediatric care.
Current problems in pediatric and adolescent health care·2026
Father and son with a pathogenic variant c.614dup p.(Gln206Thrfs*20) in the NR5A1 gene: a case report.
Frontiers in pediatrics·2026
Pediatric Spinal Cord Astrocytoma With Granular Cell-Like Morphology and KIAA1549::BRAF Fusion.
Neuropathology : official journal of the Japanese Society of Neuropathology·2026
KCTD1 p.Gly62Asp Variant in Scalp-Ear-Nipple Syndrome: Phenotypic and Structural Insights.
The Journal of craniofacial surgery·2026
Schizophrenia-associated polygenic liability and structural genomic risk demonstrate broadly distributed neuropsychiatric associations in the All of Us Research Program.
medRxiv : the preprint server for health sciences·2026