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Volumn 7, Issue 3, 2004, Pages 222-224

A three-day-old female with Carpenter's syndrome

Author keywords

Acrocephalopolysyndactyly; Carpenter's syndrome; Congenital anomaly

Indexed keywords

ACROCEPHALOPOLYSYNDACTYLY TYPE 2; ACROCEPHALOSYNDACTYLY; ARTICLE; AUTOSOMAL RECESSIVE INHERITANCE; CASE REPORT; CAUSE OF DEATH; CLINICAL FEATURE; CONSANGUINEOUS MARRIAGE; CRANIOFACIAL MALFORMATION; ECHOGRAPHY; FACE DYSMORPHIA; FEMALE; FOOT MALFORMATION; FRONTAL BOSSING; GESTATION PERIOD; HAND MALFORMATION; HUMAN; IRAN; KARYOTYPE; MICROGNATHIA; NEONATAL RESPIRATORY DISTRESS SYNDROME; NEWBORN; PRENATAL DIAGNOSIS; SYNDACTYLY;

EID: 7944237343     PISSN: 10292977     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (2)

References (8)
  • 1
    • 0032112010 scopus 로고    scopus 로고
    • A case of a four-day-old male with Carpenter's syndrome with transposition of great arteries
    • Balci S, Haytoglu T, Ozer S. A case of a four-day-old male with Carpenter's syndrome with transposition of great arteries. Turk J Pediatr. 1998; 40: 461-466.
    • (1998) Turk. J. Pediatr. , vol.40 , pp. 461-466
    • Balci, S.1    Haytoglu, T.2    Ozer, S.3
  • 2
    • 1842289791 scopus 로고    scopus 로고
    • A case of Carpenter's syndrome diagnosed in a 20-week-old fetus with postmortem examination
    • Balci S, Onol B, Eryilmaz M, Haytoglu T. A case of Carpenter's syndrome diagnosed in a 20-week-old fetus with postmortem examination. Clin Genet. 1997; 51: 412-416.
    • (1997) Clin. Genet. , vol.51 , pp. 412-416
    • Balci, S.1    Onol, B.2    Eryilmaz, M.3    Haytoglu, T.4
  • 6
    • 0023472543 scopus 로고
    • Acrocephalopolysyndactyly type II - Carpenter's syndrome: Clinical spectrum and an attempt at unification with Goodman and Summit syndromes
    • Cohen DM, Green JG, Miller J, Gorlin RJ, Reed JA. Acrocephalopolysyndactyly type II - Carpenter's syndrome: clinical spectrum and an attempt at unification with Goodman and Summit syndromes. Am J Med Genet. 1987; 28: 311-324.
    • (1987) Am. J. Med. Genet. , vol.28 , pp. 311-324
    • Cohen, D.M.1    Green, J.G.2    Miller, J.3    Gorlin, R.J.4    Reed, J.A.5
  • 7
    • 0018577709 scopus 로고
    • Craniosynostosis and syndromes with raniosynostosis: Incidence, genetics, penetrance, variability, and new syndrome updating
    • Cohen MM Jr. Craniosynostosis and syndromes with raniosynostosis: incidence, genetics, penetrance, variability, and new syndrome updating. Birth Defects Orig Artic Ser. 1979; 15: 13-63.
    • (1979) Birth. Defects. Orig. Artic. Ser. , vol.15 , pp. 13-63
    • Cohen Jr., M.M.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.