Genotypic and phenotypic analyses of Korean patients with syndromic craniosynostosis

Clinical Genetics

Volumn 76, Issue 3, 2009, Pages 287-291

  Yu, Je ^a   Jeong, S Y ^a   Yang, J A ^a   Park, M S ^a   Kim, H J ^a   Yoon, S H ^b  

^a Department of Pediatrics ^*  (South Korea)

^b Ajou University School of Medicine   (South Korea)

Author keywords

[No Author keywords available]

Indexed keywords

FIBROBLAST GROWTH FACTOR RECEPTOR 2; FIBROBLAST GROWTH FACTOR RECEPTOR 3;

ACROCEPHALOSYNDACTYLY; AMINO ACID SUBSTITUTION; ARNOLD CHIARI MALFORMATION; BEARE STEVENSON CUTIS GYRATA SYNDROME; BRACHYCEPHALY; CHILD; CLEFT PALATE; CLINICAL ARTICLE; CONGENITAL HYDROCEPHALUS; CRANIOFACIAL SYNOSTOSIS; CROUZON SYNDROME; EXOPHTHALMOS; FEMALE; GENOTYPE; GENOTYPE PHENOTYPE CORRELATION; HUMAN; INFANT; KOREA; LETTER; LIMB MALFORMATION; MALE; MISSENSE MUTATION; MUENKE SYNDROME; MUTATIONAL ANALYSIS; NUCLEIC ACID BASE SUBSTITUTION; PERCEPTION DEAFNESS; PHENOTYPE; PRIORITY JOURNAL; SEQUENCE ANALYSIS; STRABISMUS; SYNDACTYLY; SYNDROME; VERTEBRA MALFORMATION;

ABNORMALITIES, MULTIPLE; ASIAN CONTINENTAL ANCESTRY GROUP; CHILD; CHILD, PRESCHOOL; CRANIOSYNOSTOSES; FEMALE; GENOTYPE; HUMANS; INFANT; INFANT, NEWBORN; KOREA; MALE; MUTATION; PHENOTYPE; RECEPTOR, FIBROBLAST GROWTH FACTOR, TYPE 2; SYNDROME;

EID: 70350162083     PISSN: 00099163     EISSN: 13990004     Source Type: Journal    
DOI: 10.1111/j.1399-0004.2009.01201.x     Document Type: Letter

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