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Journal Abstract Search

166 related items for PubMed ID: 6491641

  • 1. [The 49,XYYYY syndrome: apropos of a case detected at birth and followed for 2 1/2 years].
    Plauchu H, Charrin C, Kossmann JC.
    J Genet Hum; 1984 Sep; 32(4):299-306. PubMed ID: 6491641
    [Abstract] [Full Text] [Related]

  • 2. A 49,XXXYY male.
    Salamanca-Gòmez F, Cortès R, Sànchez J, Armendares S.
    Am J Med Genet; 1981 Sep; 10(4):351-5. PubMed ID: 7199254
    [No Abstract] [Full Text] [Related]

  • 3. [Sex chromosome aberration with the 48 XYYY karyotype. A case report of the phenotype of a rare sex chromosome aneuploidy].
    Stein A, Heilbronner H, Jungmann J.
    Z Kinder Jugendpsychiatr; 1994 Jun; 22(2):130-4. PubMed ID: 8053267
    [Abstract] [Full Text] [Related]

  • 4. [Tetra-X syndrome with epilepsy, mental retardation and multiple dysmorphias].
    Fehlow P, Miosge W, Walther F.
    Klin Padiatr; 1993 Jun; 205(2):127-9. PubMed ID: 8487481
    [Abstract] [Full Text] [Related]

  • 5. [Two new cases of partial monosomy 11q with breakpoint in 11q24 (author's transl)].
    Laurent C, Biemont MC, Veyron M, Guilhot J, Guibaud P.
    Ann Genet; 1979 Jun; 22(4):239-41. PubMed ID: 317789
    [No Abstract] [Full Text] [Related]

  • 6. Mosaic 46, XY/47,XY, + der(18)t(Y;18)(q11.22;q11.2) karyotype, moderate mental retardation and non-specific dysmorphism.
    Fryns JP, Kleczkowska A, Van Den Berghe H.
    Genet Couns; 1990 Jun; 1(2):173-7. PubMed ID: 2081001
    [No Abstract] [Full Text] [Related]

  • 7. Sensorineural deafness in the FG syndrome: report on four new cases.
    Neri G, Blumberg B, Miles PV, Opitz JM.
    Am J Med Genet; 1984 Oct; 19(2):369-77. PubMed ID: 6542310
    [Abstract] [Full Text] [Related]

  • 8. [Chromosome X-linked mental retardation and marfanoid syndrome].
    Fryns JP, Buttiens M, van den Berghe H.
    J Genet Hum; 1988 Jan; 36(1-2):123-8. PubMed ID: 3379374
    [Abstract] [Full Text] [Related]

  • 9. The 49XXXXX syndrome. Report of a case with 48XXXX/49XXXXX mosaicism.
    Cirillo Silengo M, Davi GF, Franceschini P.
    Acta Paediatr Scand; 1979 Sep; 68(5):769-71. PubMed ID: 525347
    [Abstract] [Full Text] [Related]

  • 10. A third patient with median cleft upper lip, mental retardation and pugilistic facies (W syndrome): corroboration of a hitherto private syndrome.
    Bottani A, Schinzel A.
    Clin Dysmorphol; 1993 Jul; 2(3):225-31. PubMed ID: 8287184
    [Abstract] [Full Text] [Related]

  • 11. [48,XXYY syndrome in a boy with essential tremor. Comparison with 120 cases from the literature].
    Donati F, Gasser S, Mullis P, Braga S, Vassella F.
    Monatsschr Kinderheilkd; 1992 Apr; 140(4):216-9. PubMed ID: 1614446
    [Abstract] [Full Text] [Related]

  • 12. XYY syndrome and other Y chromosome polysomies. Mental status and psychosocial functioning.
    Fryns JP, Kleczkowska A, Kubień E, Van den Berghe H.
    Genet Couns; 1995 Apr; 6(3):197-206. PubMed ID: 8588846
    [Abstract] [Full Text] [Related]

  • 13. A chromosomal survey of an institution for the mentally retarded. Study of 476 karyotypes with banding techniques and clinical assessment of patients with chromosome anomalies.
    Nielsen KB, Dyggve HV, Knudsen H, Olsen J.
    Dan Med Bull; 1983 Feb; 30(1):5-13. PubMed ID: 6831943
    [No Abstract] [Full Text] [Related]

  • 14. [Multiple abnormalities in a child with male karyotype due to familial partial Xp duplication].
    Reichenbach H, Holland H, Thamm B, Theile T.
    Kinderarztl Prax; 1993 Oct; 61(7-8):291-5. PubMed ID: 8271681
    [Abstract] [Full Text] [Related]

  • 15. [FG syndrome in 2 half brothers].
    Wieg C, Meinecke P.
    Monatsschr Kinderheilkd; 1991 Oct; 139(10):687-9. PubMed ID: 1961207
    [Abstract] [Full Text] [Related]

  • 16. Isochromosome-formation in chromosome 9.
    Miller K, Arslan-Kirchner M.
    Ann Genet; 1994 Oct; 37(2):78-81. PubMed ID: 7985983
    [Abstract] [Full Text] [Related]

  • 17. Kabuki syndrome in son and low grade mosaic 45,X/46,XX in mother.
    Van Hagen JM, Kwee ML, Madan K, Nieuwint AW, Pals G, ten Kate LP.
    Genet Couns; 1996 Oct; 7(3):201-6. PubMed ID: 8897041
    [Abstract] [Full Text] [Related]

  • 18. MCA/MR syndrome in two female siblings: new entity or variant examples of Coffin-Lowry versus Atkin-Flaitz syndromes?
    Jans A, Ippel EF, Dijkstra PF, Bijlsma JB.
    Genet Couns; 1992 Oct; 3(3):139-43. PubMed ID: 1388932
    [Abstract] [Full Text] [Related]

  • 19. 49,XYYYY. A case report.
    Sirota L, Zlotogora Y, Shabtai F, Halbrecht I, Elian E.
    Clin Genet; 1981 Feb; 19(2):87-93. PubMed ID: 7471512
    [Abstract] [Full Text] [Related]

  • 20. [Orofaciodigital syndrome. Apropos of an 11th case in the same family].
    Vissian L, Vaillaud JC.
    Ann Dermatol Syphiligr (Paris); 1972 Feb; 99(1):5-20. PubMed ID: 5053179
    [No Abstract] [Full Text] [Related]

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