Velopharyngeal incompetence and chromosome 22q11 deletion

Lancet

Volumn 357, Issue 9258, 2001, Pages 774-

  Boorman, John G ^a   Varma, Sanjay ^a   Mackie Ogilvie, Caroline ^b  

^a QUEEN VICTORIA HOSPITAL   (United Kingdom)

^b GUY'S AND ST THOMAS' NHS FOUNDATION TRUST   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; CHROMOSOME DELETION; CLINICAL FEATURE; CONGENITAL HEART MALFORMATION; FACIES; HUMAN; MAJOR CLINICAL STUDY; NEUROLOGIC DISEASE; PALATOPHARYNGEAL INCOMPETENCE; PHENOTYPE; PRESCHOOL CHILD; PRIORITY JOURNAL; SCHOOL CHILD;

EID: 0035835975     PISSN: 01406736     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0140-6736(00)04183-0     Document Type: Article

References (5)

1. Minimum prevalence of chromosome 22q11 deletions
2. Fetal echocardiography as a predictor of chromosomal abnormality
3. Deletions and microdeletions of 22q11.2 in velo-cardio-facial syndrome
4. Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: A European collaborative study
5. Prevalence of 22q11 region deletions in patients with velopharyngeal insufficiency