A new case of syndromic craniosynostosis with cryptic 19p13.2-p13.13 deletion

American Journal of Medical Genetics, Part A

Volumn 149, Issue 11, 2009, Pages 2564-2568

  Lysy, Philippe A ^a   Ravoet, Marie ^a   Wustefeld, Sandrine ^a   Bernard, Pierre ^a   Nassogne, Marie Cécile ^a   Wyns, Elisabeth ^a   Sibille, Catherine ^a  

^a CLINIQUES UNIVERSITAIRES SAINT LUC   (Belgium)

Author keywords

[No Author keywords available]

Indexed keywords

ARTERY THROMBOSIS; ARTHROGRYPOSIS; CHROMOSOME 19Q; CHROMOSOME ABERRATION; CHROMOSOME DELETION; CLINICAL EXAMINATION; CLINODACTYLY; CRANIOFACIAL SYNOSTOSIS; ELECTROENCEPHALOGRAPHY; EXOPHTHALMOS; FLUORESCENCE IN SITU HYBRIDIZATION; GENE MUTATION; HEART ATRIUM SEPTUM DEFECT; HUMAN; HYPERTELORISM; INTRAUTERINE GROWTH RETARDATION; LETTER; LOW SET EAR; NUCHAL TRANSLUCENCY MEASUREMENT; NUCLEAR MAGNETIC RESONANCE IMAGING; PRENATAL PERIOD; PRIORITY JOURNAL; PSYCHOMOTOR DEVELOPMENT; RESPIRATORY DISTRESS; STRABISMUS; SYSTOLIC HEART MURMUR;

CHROMOSOME DELETION; COMPARATIVE GENOMIC HYBRIDIZATION; CRANIOSYNOSTOSES; FEMALE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT; INFANT, NEWBORN; MUTATION; PREGNANCY; SKULL; SYNDROME;

EID: 70449435863     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.33056     Document Type: Letter

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