메뉴 건너뛰기
Journal of the American Academy of Child and Adolescent Psychiatry
Volumn 37, Issue 11, 1998, Pages 1131-1132
Smith-Magenis syndrome [9]
Author keywords

[No Author keywords available]
Indexed keywords

CONNECTIVE TISSUE DISEASE; CYTOGENETICS; GENETIC DISORDER; HUMAN; LETTER; PRIORITY JOURNAL; SMITH MAGENIS SYNDROME;
EID: 0031736347     PISSN: 08908567     EISSN: None     Source Type: Journal    
DOI: 10.1097/00004583-199811000-00010     Document Type: Letter
Times cited : (6)
References (5)
  • 1
    • 0025218940 scopus 로고
    • Five cases demonstrating the distinctive behavioral features of chromosome deletion 17 (p.11.2 2p 11.2) (Smith-Magenis syndrome)
    • AF Colley MA Leversha LE Voullaire JG Rogers Five cases demonstrating the distinctive behavioral features of chromosome deletion 17 (p.11.2 2p 11.2) (Smith-Magenis syndrome) J Paediatr Child Health 26 1990 17 21
    • (1990) J Paediatr Child Health , vol.26 , pp. 17-21
    • Colley, AF1    Leversha, MA2    Voullaire, LE3    Rogers, JG4
  • 2
    • 0028123806 scopus 로고
    • The spasmodic upper-body squeeze: characteristic behavior in Smith-Magenis syndrome
    • BM Finucane D Konar B Haas-Givler MB Kurtz CI Scott Jr The spasmodic upper-body squeeze: characteristic behavior in Smith-Magenis syndrome Dev Med Child Neurol 36 1994 78 83
    • (1994) Dev Med Child Neurol , vol.36 , pp. 78-83
    • Finucane, BM1    Konar, D2    Haas-Givler, B3    Kurtz, MB4    Scott, CI5
  • 3
    • 0026347929 scopus 로고
    • Molecular analysis of the Smith-Magenis syndrome: a possible contiguous-gene syndrome associated with del(17)(p 11.2)
    • F Greenberg V Guzzetta R Montes de Oca-Luna Molecular analysis of the Smith-Magenis syndrome: a possible contiguous-gene syndrome associated with del(17)(p 11.2) Am J Hum Genet 49 1991 1207 1218
    • (1991) Am J Hum Genet , vol.49 , pp. 1207-1218
    • Greenberg, F1    Guzzetta, V2    Montes de Oca-Luna, R3
  • 4
    • 0022543280 scopus 로고
    • Interstitial deletion of (17)(p11.2p 11.2) in nine patients
    • ACM Smith L McGavran J Robinson Interstitial deletion of (17)(p11.2p 11.2) in nine patients Am J Med Genet 24 1986 393 414
    • (1986) Am J Med Genet , vol.24 , pp. 393-414
    • Smith, ACM1    McGavran, L2    Robinson, J3
  • 5
    • 0001403971 scopus 로고
    • Deletion of the 17 short arm in two patients with facial clefts
    • ACM Smith L McGavran G Waldstein Deletion of the 17 short arm in two patients with facial clefts Am J Hum Genet 34 suppl 1982 A4l0
    • (1982) Am J Hum Genet , vol.34 , Issue.suppl , pp. A4l0
    • Smith, ACM1    McGavran, L2    Waldstein, G3

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.