No evidence of unbalanced growth-related gene inheritance in a series of overgrowth syndrome patients [4]

American Journal of Medical Genetics

Volumn 99, Issue 2, 2001, Pages 166-167

  Faivre, Laurence ^a   Vekemans, Michel ^a   Sanlaville, Damien ^a   Munnich, Arnold ^a   Cormier Daire, Valérie ^a  

^a HÔPITAL NECKER ENFANTS MALADES   (France)

Author keywords

[No Author keywords available]

Indexed keywords

MICROSATELLITE DNA; SOMATOSTATIN RECEPTOR;

BECKWITH WIEDEMANN SYNDROME; CHROMOSOME MOSAICISM; GENE DOSAGE; GENE DUPLICATION; GENE LOCUS; GIGANTISM; HUMAN; INHERITANCE; LETTER; PHENOTYPE; PRIORITY JOURNAL; SIMPSON GOLABI BEHMEL SYNDROME; SOTOS SYNDROME; TRISOMY; TRISOMY 20; WEAVER SYNDROME;

CHROMOSOME MAPPING; GROWTH DISORDERS; HUMANS; SYNDROME;

EID: 0035281864     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/1096-8628(2000)9999:999<00::AID-AJMG1140>3.0.CO;2-O     Document Type: Letter

References (10)

1. SHOX mutations in dyschondrosteosis (Léri-Weill syndrome)
2. A comprehensive genetic map on the human genome based on 5,264 microsatellites
3. Syndrome of the month: Beckwith-Wiedeman syndrome
4. Apparent Sotos syndrome (cerebral gigantism) in a child with trisomy 20p11.2-p12.1 mosaicism
5. Partial trisomy 15(q25qter) in two brothers
6. Molecular genetics of Wiedemann-Beckwith syndrome
7. Clinical and molecular aspects of the Simpson-Golabi-Behmel syndrome
8. Translocations involving 4p16.3 in three families: Deletion causing the Pitt-Rogers-Danks syndrome and duplication resulting in a new overgrowth syndrome
9. No evidence for uniparental disomy as a common cause of Sotos syndrome
10. Partial duplication of the long arm of chromosome 15: Confirmation of a causative role in craniosynostosis and definition of a 15q25-qter trisomy syndrome