Mosaic trisomy 8 as a cause of velopharyngeal insufficiency [1]

American Journal of Medical Genetics

Volumn 108, Issue 4, 2002, Pages 337-338

  Vantrappen, Greet ^a   Rommel, Nathalie ^b   Cremers, Cor W R J ^a   Fryns, Jean Pierre ^a   Devriendt, Koen ^a  

^a UNIVERSITY HOSPITALS LEUVEN   (Belgium)

^b RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

CASE REPORT; CLINICAL FEATURE; FEMALE; HUMAN; IMAGE ANALYSIS; LETTER; MALE; PALATOPHARYNGEAL INCOMPETENCE; PATHOGENESIS; PHARYNGOGRAPHY; PHARYNX RECONSTRUCTION; PRESCHOOL CHILD; PRIORITY JOURNAL; SPEECH THERAPY; TRISOMY 8;

CHROMOSOMES, HUMAN, PAIR 8; FEMALE; HUMANS; INFANT, NEWBORN; MALE; MOSAICISM; SPEECH DISORDERS; TRISOMY; VELOPHARYNGEAL INSUFFICIENCY;

EID: 0036532247     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.10270     Document Type: Letter

References (7)

1. A chromosomal duplication map of malformations: Regions of suspected haplo- and triplolethality- and tolerance of segmental aneuploidy-in humans
2. The oro-facial manifestations of trisomy 8 mosaicism: A case report
3. Presence of 22qll deletion in postadenoidectomy velopharyngeal insufficiency
4. Retrospective analysis of feeding and speech disorders in 50 patients with velo-cardio-facial syndrome
5. Velocardiofacial syndrome
6. Prevalence of 22qll region deletions in patients with velopharyngeal insufficiency