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Journal Abstract Search

71 related items for PubMed ID: 6680431

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  • 6. Craniosynostosis in the Ullrich-Turner syndrome.
    Heinrichs C, Elmer C, Derasse M, Perlmutter N, Vamos E.
    Am J Med Genet; 1991 Aug 01; 40(2):252. PubMed ID: 1760044
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  • 7. Monosomy X associated with fra(17p12) and 22p-.
    Izakovic V.
    Clin Genet; 1984 Aug 01; 26(2):165-6. PubMed ID: 6467670
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  • 10. Growth-promoting strategies in Turner's syndrome.
    Saenger P.
    J Clin Endocrinol Metab; 1999 Dec 01; 84(12):4345-8. PubMed ID: 10599686
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  • 14. [Turner syndrome caused by deletion of the long arm of the X chromosome associated with adrenogenital syndrome caused by partial deficiency of 21-hydroxylase].
    del Arbol JL, Soto Más JA, Fernández-Abril JA, Raya Muñoz J, Martínez Tormo F, Gómez Rodríguez J, Gómez Capilla JA, Peña Yáñez A.
    Rev Clin Esp; 1983 Oct 15; 171(1):67-71. PubMed ID: 6606833
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  • 15. Growth curves in untreated Ullrich-Turner syndrome: French reference standards 1-22 years.
    Sempé M, Hansson Bondallaz C, Limoni C.
    Eur J Pediatr; 1996 Oct 15; 155(10):862-9. PubMed ID: 8891555
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  • 16. Prevalence of the 45, X karyotype among Turner syndrome patients.
    Beiguelman B, Pinto Júnior W, Barcelos KA.
    Genet Couns; 1996 Oct 15; 7(3):231-2. PubMed ID: 8897046
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  • 17. [Normal 46,XX daughter born to a 45,X/46,X,del(X)(q25) deletion (author's transl)].
    de Grouchy J, Thibaud E, Turleau C, Roubin M, Rose F, Cachin O, Rappaport R.
    Ann Genet; 1981 Oct 15; 24(4):229-30. PubMed ID: 6977304
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  • 18. Human genetics. A father's imprint on his daughter's thinking.
    McGuffin P, Scourfield J.
    Nature; 1997 Jun 12; 387(6634):652-3. PubMed ID: 9192882
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  • 20. A clinical and cytogenetic study of Turner syndrome.
    Suri M, Kabra M, Jain U, Sanders V, Saxena R, Shukla A, Singh GV, Verma IC.
    Indian Pediatr; 1995 Apr 12; 32(4):433-42. PubMed ID: 8635807
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