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Journal Abstract Search

331 related items for PubMed ID: 2370045

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  • 7. Molecular definition of Xq common-deleted region in patients affected by premature ovarian failure.
    Marozzi A, Manfredini E, Tibiletti MG, Furlan D, Villa N, Vegetti W, Crosignani PG, Ginelli E, Meneveri R, Dalprà L.
    Hum Genet; 2000 Oct; 107(4):304-11. PubMed ID: 11129329
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  • 8. Ovarian differentiation and gonadal failure.
    Simpson JL, Rajkovic A.
    Am J Med Genet; 1999 Dec 29; 89(4):186-200. PubMed ID: 10727994
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  • 14. Structural anomalies of the X chromosome: personal observation and review of non-mosaic cases.
    Wyss D, DeLozier CD, Daniell J, Engel E.
    Clin Genet; 1982 Feb 29; 21(2):145-59. PubMed ID: 7044622
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  • 15. Structural aberrations of the X chromosome in man.
    Davidenkova EF, Verlinskaja DK, Mashkova MV.
    Hum Genet; 1978 Apr 24; 41(3):269-79. PubMed ID: 649155
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  • 16. Further dicentric X isochromosomes and deletions, and a new structure i(X)(pter to q2102 to pter).
    Daniel A, Saville T, Southall DB.
    J Med Genet; 1979 Aug 24; 16(4):278-84. PubMed ID: 490580
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  • 17. [Chromosome X with partial long arm deletion. Three cases].
    Teyssier M, Charrin C.
    J Gynecol Obstet Biol Reprod (Paris); 1992 Aug 24; 21(4):413-7. PubMed ID: 1624728
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  • 18. Del (X)(p21.2) in a mother and two daughters with variable ovarian function.
    Zinn AR, Ouyang B, Ross JL, Varma S, Bourgeois M, Tonk V.
    Clin Genet; 1997 Oct 24; 52(4):235-9. PubMed ID: 9383030
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