Role of rare cases in deciphering the mechanisms of congenital anomalies: CHARGE syndrome research

Congenital Anomalies

Volumn 51, Issue 1, 2011, Pages 12-15

  Kosaki, Kenjiro ^a  

^a KEIO UNIVERSITY SCHOOL OF MEDICINE   (Japan)

Author keywords

CHARGE syndrome; CHD7; Dysmorphology; London Dysmorphology Database; Methimazole embryopathy

Indexed keywords

BIRTH DEFECT; CHD7 GENE; CHICK EMBRYO; COLOBOMA; DIGEORGE SYNDROME; EAR MALFORMATION; EMBRYO; FACE ASYMMETRY; FACIAL NERVE PARALYSIS; GENE; GENE EXPRESSION; GENE MUTATION; GENETIC ANALYSIS; GENETIC CORRELATION; GENOMIC IN SITU HYBRIDIZATION; HUMAN; KALLMANN SYNDROME; MENTAL DEFICIENCY; NONHUMAN; PHENOTYPE; PRIORITY JOURNAL; REVIEW; SYNDROME CHARGE;

ANIMALS; CHARGE SYNDROME; CHICK EMBRYO; DNA HELICASES; DNA-BINDING PROTEINS; FEMALE; HUMANS; IN SITU HYBRIDIZATION; MALE; MATERNAL EXPOSURE; METHIMAZOLE; NEURAL CREST; PREGNANCY; PRENATAL EXPOSURE DELAYED EFFECTS;

ANIMALIA;

EID: 79951805635     PISSN: 09143505     EISSN: 17414520     Source Type: Journal    
DOI: 10.1111/j.1741-4520.2010.00309.x     Document Type: Review

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