No justification of routine screening for 22q11 deletions in patients with overt cleft palate

Clinical Genetics

Volumn 64, Issue 3, 2003, Pages 216-219

  Ruiter, E M ^a   Bongers, E M H F ^a   Smeets, D F C M ^a   Kuijpers Jagtman, A M ^a   Hamel, B C J ^a  

^a RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

Author keywords

Cleft palate; Deletion 22q11; Screening; Velo cardio facial syndrome; Velopharyngeal insufficiency

Indexed keywords

ARTICLE; CHILD GROWTH; CHROMOSOME 22Q; CHROMOSOME ANALYSIS; CHROMOSOME DELETION; CLEFT PALATE; CLINICAL FEATURE; EARLY DIAGNOSIS; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; FOLLOW UP; GENETIC SCREENING; HEALTH CENTER; HUMAN; MAJOR CLINICAL STUDY; MALE; MEDICAL LITERATURE; NETHERLANDS; NEWBORN; PREVALENCE; PRIORITY JOURNAL; SYMPTOM; VELOCARDIOFACIAL SYNDROME;

ABNORMALITIES, MULTIPLE; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 22; CLEFT PALATE; FEMALE; GENETIC SCREENING; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INCIDENCE; INFANT; INFANT, NEWBORN; MALE; NEONATAL SCREENING; NETHERLANDS; PREVALENCE; SYNDROME; UNNECESSARY PROCEDURES;

EID: 0042914406     PISSN: 00099163     EISSN: None     Source Type: Journal    
DOI: 10.1034/j.1399-0004.2003.00134.x     Document Type: Article

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