메뉴 건너뛰기




Volumn 143, Issue 13, 1999, Pages 682-686

Trisomy 9p: Clinical picture and importance of examination of family;Trisomie 9p: Klinisch beeld en het belang van familieonderzoek

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; BRACHYCEPHALY; CASE REPORT; CHROMOSOME TRANSLOCATION; CLINICAL FEATURE; CLINODACTYLY; FACE MALFORMATION; FAMILY PLANNING; FEMALE; GENETIC COUNSELING; HUMAN; HYPERTELORISM; INFANT; MALE; MENTAL DEFICIENCY; PARTIAL TRISOMY 9; PRENATAL DIAGNOSIS; RISK ASSESSMENT;

EID: 0033608695     PISSN: 00282162     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (3)

References (18)
  • 2
    • 0026647257 scopus 로고
    • High prevalence of the fra(X) syndrome cannot be explained by a high mutation rate
    • Smits A, Smeets D, Hamel B, Dreesen J. Oost B van. High prevalence of the fra(X) syndrome cannot be explained by a high mutation rate. Am J Med Genet 1992;43:345-52.
    • (1992) Am J Med Genet , vol.43 , pp. 345-352
    • Smits, A.1    Smeets, D.2    Hamel, B.3    Dreesen, J.4    Van Oost, B.5
  • 3
    • 0017179589 scopus 로고
    • Partial and complete trisomy 9: Delineation of a trisomy 9 syndrome
    • Sutherland GR, Carter RF, Morris LL, Partial and complete trisomy 9: delineation of a trisomy 9 syndrome. Hum Genet 1976;32:1 33-40.
    • (1976) Hum Genet , vol.32 , pp. 133-140
    • Sutherland, G.R.1    Carter, R.F.2    Morris, L.L.3
  • 4
    • 0017620566 scopus 로고
    • The distal 9p trisomy syndrome: A major clinical-cytogenetic entity
    • Centerwall WR. The distal 9p trisomy syndrome: a major clinical-cytogenetic entity. Birth Defects Orig Artic Ser 1977;13:165-77.
    • (1977) Birth Defects Orig Artic Ser , vol.13 , pp. 165-177
    • Centerwall, W.R.1
  • 7
    • 0020475051 scopus 로고
    • Diagnostiek en preventie van chromosoomafwijkingen
    • Sachs ES, Hemel JO van. Diagnostiek en preventie van chromosoomafwijkingen. Ned Tijdschr Geneeskd 1982;126:2236-44.
    • (1982) Ned Tijdschr Geneeskd , vol.126 , pp. 2236-2244
    • Sachs, E.S.1    Van Hemel, J.O.2
  • 9
    • 0014914222 scopus 로고
    • Sur quatre cas de trisomie pour le bras court du chromosome 9. Individualisation d'une nouvelle entite morbide
    • Rethoré MO, Larget-Piet L, Abonyi D, Boeswillwald M, Berger R, Carpentier S, et al. Sur quatre cas de trisomie pour le bras court du chromosome 9. Individualisation d'une nouvelle entite morbide. Ann Genet 1970;13:217-32.
    • (1970) Ann Genet , vol.13 , pp. 217-232
    • Rethoré, M.O.1    Larget-Piet, L.2    Abonyi, D.3    Boeswillwald, M.4    Berger, R.5    Carpentier, S.6
  • 11
    • 0021921021 scopus 로고
    • The phenotypic and cytogenetic spectrum of partial trisomy 9
    • Wilson GN, Raj A, Baker D. The phenotypic and cytogenetic spectrum of partial trisomy 9. Am J Med Genet 1985;20:277-82.
    • (1985) Am J Med Genet , vol.20 , pp. 277-282
    • Wilson, G.N.1    Raj, A.2    Baker, D.3
  • 12
    • 0019872401 scopus 로고
    • Ecn zwakzinnige man met vele aangeboren afwijkingen, epilepsie en trisomie 9p en partiële monosomie 17q
    • Linden GJ van der, Dumoré-Balek A, Veenema H, Geraedts JPM. Ecn zwakzinnige man met vele aangeboren afwijkingen, epilepsie en trisomie 9p en partiële monosomie 17q. Ned Tijdschr Geneeskd 1981;125:540-3.
    • (1981) Ned Tijdschr Geneeskd , vol.125 , pp. 540-543
    • Van Der Linden, G.J.1    Dumoré-Balek, A.2    Veenema, H.3    Geraedts, J.P.M.4
  • 14
    • 0018414643 scopus 로고
    • Trisomy 9p. A chromosome aberration with distinct radiologic findings
    • Schinzel A. Trisomy 9p. a chromosome aberration with distinct radiologic findings. Radiology 1979;130:125-33.
    • (1979) Radiology , vol.130 , pp. 125-133
    • Schinzel, A.1
  • 16
    • 0017288520 scopus 로고
    • Familial 'partial 9p' trisomy: Six cases and four carriers in three generations
    • Centerwall WR, Miller KS, Reeves LM, Familial 'partial 9p' trisomy: six cases and four carriers in three generations. J Med Genet 1976;13:57-61.
    • (1976) J Med Genet , vol.13 , pp. 57-61
    • Centerwall, W.R.1    Miller, K.S.2    Reeves, L.M.3
  • 18
    • 0020039076 scopus 로고
    • Genetic risks for familial reciprocal translocations with special emphasis on those leading to 9p. top and 12p trisomies
    • Stene J, Stengel-Rutkowski S. Genetic risks for familial reciprocal translocations with special emphasis on those leading to 9p. top and 12p trisomies. Ann Hum Genet 1982:46(Pt 1):41-74.
    • (1982) Ann Hum Genet , vol.46 , Issue.PT 1 , pp. 41-74
    • Stene, J.1    Stengel-Rutkowski, S.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.