Autosomal dominant isolated velopharyngeal insufficiency [2]

Clinical Genetics

Volumn 61, Issue 1, 2002, Pages 74-76

  Vantrappen, Greet ^a   Rommel, N ^b   Wellens, W ^b   Cremers, C W R J ^b   Fryns, J P ^b   Devriendt, K ^b  

^a UNIVERSITY HOSPITALS LEUVEN   (Belgium)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; AUTOSOMAL DOMINANT INHERITANCE; CASE REPORT; CHILD; CHROMOSOME 22Q; CHROMOSOME ANALYSIS; CHROMOSOME DELETION; FAMILY HISTORY; FEMALE; HUMAN; LETTER; MALE; PALATOPHARYNGEAL INCOMPETENCE; PHARYNX RECONSTRUCTION; PRIORITY JOURNAL; SIBLING; SPEECH DISORDER; SPEECH THERAPY;

CHILD; CHILD, PRESCHOOL; FEMALE; GENES, DOMINANT; HUMANS; MALE; MIDDLE AGED; PALATE, SOFT; PEDIGREE; SPEECH DISORDERS; VELOPHARYNGEAL INSUFFICIENCY;

EID: 0036461426     PISSN: 00099163     EISSN: None     Source Type: Journal    
DOI: 10.1034/j.1399-0004.2002.610115.x     Document Type: Letter

References (4)

1. Andres R, Bixler D, Shanks J et al. Dominant inheritance of velopharyngeal incompetence. Clin Genet 1981: 19: 443-447.
2. Zori RT, Boyar FZ, Williams WN et al. Prevalence of 22q11 region deletions in patients with velopharyngeal insufficiency. Am J Med Genet 1998: 28: 7 (1): 8-11.
3. Shprintzen RJ. Velocardiofacial syndrome. Otolaryngol Clin North Am 2000: 33: 1217-1240.
4. Ryan A, Goodship JA, Wilson D et al. Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study. J Med Genet 1997: 34: 798-804.