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Volumn 148, Issue 1, 2000, Pages 55-69

Chromosomal microdeletion syndrome;Chromosomale mikrodeletionssyndrome

Author keywords

[No Author keywords available]

Indexed keywords

CHROMOSOME 22Q; CHROMOSOME ANALYSIS; CHROMOSOME DELETION; CYTOGENETICS; DIGEORGE SYNDROME; FLUORESCENCE IN SITU HYBRIDIZATION; HAPPY PUPPET SYNDROME; HUMAN; MILLER DIEKER SYNDROME; PRADER WILLI SYNDROME; REVIEW; SMITH MAGENIS SYNDROME; VELOCARDIOFACIAL SYNDROME; WILLIAMS BEUREN SYNDROME;

EID: 0034107262     PISSN: 00269298     EISSN: None     Source Type: Journal    
DOI: 10.1007/s001120050015     Document Type: Review
Times cited : (2)

References (8)
  • 5
    • 0032916681 scopus 로고    scopus 로고
    • Williams-Beuren syndrome: An update and review for the primary physician
    • Lashkari A, Smith AK, Graham JM (1999) Williams-Beuren syndrome: an update and review for the primary physician. Clin Pediatr 38:189-208
    • (1999) Clin Pediatr , vol.38 , pp. 189-208
    • Lashkari, A.1    Smith, A.K.2    Graham, J.M.3
  • 6
    • 0031132215 scopus 로고    scopus 로고
    • Chromosome 22q11 deletion syndrome: An update and review for the primary pediatrician
    • Thomas JA, Graham JM (1997) Chromosome 22q11 deletion syndrome: an update and review for the primary pediatrician. Clin Pediatr 36:253-266
    • (1997) Clin Pediatr , vol.36 , pp. 253-266
    • Thomas, J.A.1    Graham, J.M.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.