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Volumn 132 A, Issue 2, 2005, Pages 223-225

Mosaic trisomy 22: Report of a patient with normal intelligence [6]

Author keywords

[No Author keywords available]

Indexed keywords

CHROMOSOME BANDING PATTERN; CHROMOSOME MOSAICISM; CLINICAL FEATURE; CYTOGENETICS; DERMATOGLYPHICS; FAMILY HISTORY; HUMAN; INCIDENCE; INTELLIGENCE; LETTER; LYMPHOCYTE CULTURE; PREGNANCY; PRIORITY JOURNAL; SPONTANEOUS ABORTION; TRISOMY; TRISOMY 22;

EID: 11844255395     PISSN: 15524825     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.a.30401     Document Type: Letter
Times cited : (16)

References (20)
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    • Mosaic Trisomy 22: A case presentation and literature review of Trisomy 22 phenotypes
    • Crowe CA, Schwartz S, Black CJ, Jaswaney V. 1997. Mosaic Trisomy 22: A case presentation and literature review of Trisomy 22 phenotypes. Am J Med Genet 71:406-413.
    • (1997) Am J Med Genet , vol.71 , pp. 406-413
    • Crowe, C.A.1    Schwartz, S.2    Black, C.J.3    Jaswaney, V.4
  • 7
    • 33646217346 scopus 로고    scopus 로고
    • Clinical diagnosis of Down syndrome using dermatoglyphics: A wonderful but underused method
    • Lacassie Y. 2004. Clinical diagnosis of Down syndrome using dermatoglyphics: A wonderful but underused method. Genet Med 6:297 (108A).
    • (2004) Genet Med , vol.6 , pp. 297
    • Lacassie, Y.1
  • 8
    • 0023807569 scopus 로고
    • Trisomy 22 mosaicism with normal blood chromosomes
    • Lessick ML, Szego K, Wong PWK. 1988. Trisomy 22 mosaicism with normal blood chromosomes. Clin Pediatr 27:451-454.
    • (1988) Clin Pediatr , vol.27 , pp. 451-454
    • Lessick, M.L.1    Szego, K.2    Wong, P.W.K.3
  • 9
    • 0025295061 scopus 로고
    • Trisomy 22 mosaicism limited to skin fibroblasts in a mentally retarded, dysmorphic girl
    • Lund HT, Tranebjaerg L. 1990. Trisomy 22 mosaicism limited to skin fibroblasts in a mentally retarded, dysmorphic girl. Acta Paediatr Scand 79:714-718.
    • (1990) Acta Paediatr Scand , vol.79 , pp. 714-718
    • Lund, H.T.1    Tranebjaerg, L.2
  • 12
    • 33646223182 scopus 로고
    • Trisomy 22 mosaicism: Part of the differential diagnosis of Noonan and Turner's syndrome phenotype
    • Pagon RA, Hall JG, Hoehn H. 1977. Trisomy 22 mosaicism: Part of the differential diagnosis of Noonan and Turner's syndrome phenotype. Am J Med Genet 29:85A.
    • (1977) Am J Med Genet , vol.29
    • Pagon, R.A.1    Hall, J.G.2    Hoehn, H.3
  • 13
    • 0018340524 scopus 로고
    • Abnormal skin fibroblast cytogenetics in four dysmorphic patients with normal lymphocyte chromosomes
    • Pagon RA, Hall JG, Davenport SLH, Aase J, Norwood TH, Hoehn WH. 1979. Abnormal skin fibroblast cytogenetics in four dysmorphic patients with normal lymphocyte chromosomes. Am J Med Genet 31:54-61.
    • (1979) Am J Med Genet , vol.31 , pp. 54-61
    • Pagon, R.A.1    Hall, J.G.2    Davenport, S.L.H.3    Aase, J.4    Norwood, T.H.5    Hoehn, W.H.6
  • 15
  • 16
    • 0019422087 scopus 로고
    • Incomplete Trisomy 22. III. Mosaic-Trisomy 22 and the problem of full Trisomy 22
    • Schinzel A. 1981. Incomplete Trisomy 22. III. Mosaic-Trisomy 22 and the problem of full Trisomy 22. Hum Genet 56:269-273.
    • (1981) Hum Genet , vol.56 , pp. 269-273
    • Schinzel, A.1
  • 19
    • 0029950129 scopus 로고    scopus 로고
    • Confined placental mosaicism for trisomies 2, 3, 7, 8, 9, 16 and 22: Their incidence, likely origins, and mechanisms for cell lineage compartmentalization
    • Wolstenholme J. 1996. Confined placental mosaicism for trisomies 2, 3, 7, 8, 9, 16 and 22: Their incidence, likely origins, and mechanisms for cell lineage compartmentalization. Prenat Diagn 16:511-524.
    • (1996) Prenat Diagn , vol.16 , pp. 511-524
    • Wolstenholme, J.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.