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Volumn 119 A, Issue 2, 2003, Pages 234-237

Male patient with non-mosaic deleted Y-chromosome and clinical features of Turner syndrome

Author keywords

Deleted Ychromosome; Male Turner; Marker Y chromosome; Turner syndrome

Indexed keywords

ARTICLE; CASE REPORT; CHILD; CHROMOSOME DELETION; CHROMOSOME MARKER; CHROMOSOME REARRANGEMENT; CLINICAL FEATURE; GENETIC ASSOCIATION; GENOTYPE; HUMAN; MALE; MOSAICISM; PHENOTYPE; PRIORITY JOURNAL; SEX CHROMOSOMAL INHERITANCE; SHORT STATURE; TURNER SYNDROME; X CHROMOSOME INACTIVATION; Y CHROMOSOME;

EID: 0042823484     PISSN: 15524825     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.a.10147     Document Type: Article
Times cited : (10)

References (11)
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    • (1965) J Med Genet , vol.2 , pp. 142
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  • 4
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    • The distribution of chromosomal genotypes associated with Turner syndrome: Livebirth prevalence rates and evidence for diminished fetal mortality and severity in genotypes associated with structural X abnormalities or mosaicism
    • Hook EB, Warburton D. 1983. The distribution of chromosomal genotypes associated with Turner syndrome: Livebirth prevalence rates and evidence for diminished fetal mortality and severity in genotypes associated with structural X abnormalities or mosaicism. Hum Genet 64:24-27.
    • (1983) Hum Genet , vol.64 , pp. 24-27
    • Hook, E.B.1    Warburton, D.2
  • 6
    • 0030960829 scopus 로고    scopus 로고
    • Development and clinical application of an innovative fluorescence in situ hybridization technique which detects submicroscopic rearrangements involving telomeres
    • Knight SJ, Horsley SW, Regan R, Lawrie NM, Maher EJ, Cardy DL, Flint J, Kearney L. 1997. Development and clinical application of an innovative fluorescence in situ hybridization technique which detects submicroscopic rearrangements involving telomeres. Eur J Hum Genet 5:1-8.
    • (1997) Eur J Hum Genet , vol.5 , pp. 1-8
    • Knight, S.J.1    Horsley, S.W.2    Regan, R.3    Lawrie, N.M.4    Maher, E.J.5    Cardy, D.L.6    Flint, J.7    Kearney, L.8
  • 8
    • 0029033299 scopus 로고
    • Clinical features of nine males with molecularly defined deletions of the Y chromosome long arm
    • Salo P, Ignatius J, Simola KO, Tahvanainen E, Kaariainen H. 1995. Clinical features of nine males with molecularly defined deletions of the Y chromosome long arm. J Med Genet 32:711-715.
    • (1995) J Med Genet , vol.32 , pp. 711-715
    • Salo, P.1    Ignatius, J.2    Simola, K.O.3    Tahvanainen, E.4    Kaariainen, H.5
  • 9
    • 0033005691 scopus 로고    scopus 로고
    • Two male patients with ring Y: Definition of an interval in Yq contributing to Turner syndrome
    • Tzancheva M, Kaneva R, Kumanov P, Williams G, Tyler-Smith C. 1999. Two male patients with ring Y: definition of an interval in Yq contributing to Turner syndrome. J Med Genet 36:549-553.
    • (1999) J Med Genet , vol.36 , pp. 549-553
    • Tzancheva, M.1    Kaneva, R.2    Kumanov, P.3    Williams, G.4    Tyler-Smith, C.5
  • 10
    • 0032103696 scopus 로고    scopus 로고
    • Turner syndrome and haploinsufficiency
    • Zinn AR, Ross JL. 1998. Turner syndrome and haploinsufficiency. Curr Opin Genet Dev 8:322-327.
    • (1998) Curr Opin Genet Dev , vol.8 , pp. 322-327
    • Zinn, A.R.1    Ross, J.L.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.