Small deletion - Large effect;Kleine Deletion - Große Auswirkung

HNO

Volumn 52, Issue 3, 2004, Pages 258-260

  Luerssen K ^a   Pruggmayer, M ^a   Ptok, M ^a  

^a HANNOVER MEDICAL SCHOOL   (Germany)

Author keywords

Deletion 22q11; DiGeorge symdrome; Genetic examination; Shprintzen's syndrome; Velocardiofacial syndrome

Indexed keywords

ARTICLE; CHROMOSOME 22Q; CLEFT PALATE; CONGENITAL HEART MALFORMATION; DIGEORGE SYNDROME; EARLY DIAGNOSIS; FACE DYSMORPHIA; FLUORESCENCE IN SITU HYBRIDIZATION; GENETIC ANALYSIS; HUMAN; LEARNING DISORDER; MIDDLE EAR MALFORMATION; MONOSOMY; PHENOTYPE; PROGNOSIS; VELOCARDIOFACIAL SYNDROME; CHILD; CHROMOSOME 22; CHROMOSOME DELETION; CRANIOFACIAL MALFORMATION; DIFFERENTIAL DIAGNOSIS; FACIES; GENETICS; SYNDROME;

CHILD; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 22; CLEFT PALATE; CRANIOFACIAL ABNORMALITIES; DIAGNOSIS, DIFFERENTIAL; DIGEORGE SYNDROME; FACIES; HEART DEFECTS, CONGENITAL; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; SYNDROME;

EID: 4344634968     PISSN: 00176192     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00106-003-0954-3     Document Type: Article

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