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Volumn 63, Issue 3, 1998, Pages 901-905

Swyer syndrome and 46,XY partial gonadal dysgenesis associated with 9p deletions in the absence of monosomy-9p syndrome [3]

Author keywords

[No Author keywords available]

Indexed keywords

CHROMOSOME 9P; GENE DELETION; GENOTYPE; GONADAL DYSGENESIS; HUMAN; LETTER; LONG PHILTRUM; MENTAL DEFICIENCY; NUCLEOTIDE REPEAT; PARTIAL MONOSOMY; PRIORITY JOURNAL; WEBBED NECK;

EID: 0032231944     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/302023     Document Type: Letter
Times cited : (67)

References (15)
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  • 3
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    • Monosomie 9p2
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    • (1970) Clin Genet , vol.1 , pp. 27-57
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  • 6
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    • R Ion L Telvi JL Chaussain JP Barbet M Nunes A Safar MO Rethore Failure of testicular development associated with a rearrangement of 9p24.1 proximal to the SNF2 gene Hum Genet 102 1998 151 156
    • (1998) Hum Genet , vol.102 , pp. 151-156
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  • 8
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    • T Ogata K Muroya N Matsuo J Hata Y Fukushima Y Suzuki Impaired male sex development in an infant with molecularly defined 9p partial monosomy: implication for a testis forming gene (s) on 9p J Med Genet 34 1997 331 334
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  • 10
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    • A Schinzel Catalogue of unbalanced chromosome aberrations in man 1984 De Gruyter New York
    • (1984)
    • Schinzel, A1
  • 11
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    • (1997) Ann Hum Genet , vol.61 , pp. 222
    • Schwartz, S1    Crowe, CA2    Conroy, JM3    Haren, JM4    Micale, MA5    Becker, LA6
  • 12
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    • A conserved gene from the human sex-determining region encodes a protein with homology to a conserved DNA-binding motif
    • AH Sinclair P Berta MS Palmer R Hawkins BL Griffiths MJ Smith JW Foster A conserved gene from the human sex-determining region encodes a protein with homology to a conserved DNA-binding motif Nature 346 1990 240 244
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  • 14
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    • aMutations and sequence variants in the testis determining region of the Y chromosome in individuals with a 46,XY female phenotype
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  • 15
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.