The Velocardiofacial syndrome: A review

Genetic Counseling

Volumn 13, Issue 2, 2002, Pages 105-113

  Vogels, A ^a   Fryns, J P ^a  

^a CENTER FOR HUMAN GENETICS   (Belgium)

Author keywords

22q11 deletion; Behavioural phenotype; Clinical phenotype; COMT; Microdeletion; Mouse models; PRODH; VECF REPS; Velocardiofacial syndrome

Indexed keywords

ANIMAL MODEL; CHROMOSOME 22Q; CHROMOSOME DELETION; CLINICAL FEATURE; CROSSING OVER; GENE CLUSTER; GENE DOSAGE; GENETIC PREDISPOSITION; MISSENSE MUTATION; MOLECULAR GENETICS; PHENOTYPE; REVIEW; VELOCARDIOFACIAL SYNDROME; ANIMAL; BRANCHIAL ARCH; CHROMOSOME 22; CONGENITAL MALFORMATION; DISEASE MODEL; FACE; GENETICS; HUMAN; MOUSE; MULTIPLE MALFORMATION SYNDROME; PARATHYROID GLAND; PATHOLOGY; SYNDROME; THORACIC AORTA; THYMUS;

ABNORMALITIES, MULTIPLE; ANIMAL; AORTA, THORACIC; BRANCHIAL REGION; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 22; DISEASE MODELS, ANIMAL; FACE; HUMAN; MICE; PARATHYROID GLANDS; SYNDROME; THYMUS GLAND; ANIMALS; HUMANS;

EID: 0035985762     PISSN: 10158146     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Review

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