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Journal Abstract Search

117 related items for PubMed ID: 7400886

  • 1. Embryonic testicular regression syndrome: variable phenotypic expression in siblings.
    Josso N, Briard ML.
    J Pediatr; 1980 Aug; 97(2):200-4. PubMed ID: 7400886
    [Abstract] [Full Text] [Related]

  • 2. Embryonic testicular regression syndrome and severe mental retardation in sibs.
    de Grouchy J, Gompel A, Salomon-Bernard Y, Kuttenn F, Yaneva H, Paniel JB, Le Merrer M, Roubin M, Doussau de Bazignan M, Turleau C.
    Ann Genet; 1985 Aug; 28(3):154-60. PubMed ID: 3879148
    [Abstract] [Full Text] [Related]

  • 3. Management of phenotypic female patients with an XY karyotype.
    Portuondo JA, Neyro JL, Barral A, Gonzalez-Gorospe F, Benito JA.
    J Reprod Med; 1986 Jul; 31(7):611-5. PubMed ID: 3091820
    [Abstract] [Full Text] [Related]

  • 4. Clinical and pathologic spectrum of 46,XY gonadal dysgenesis: its relevance to the understanding of sex differentiation.
    Berkovitz GD, Fechner PY, Zacur HW, Rock JA, Snyder HM, Migeon CJ, Perlman EJ.
    Medicine (Baltimore); 1991 Nov; 70(6):375-83. PubMed ID: 1956279
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  • 5. A new familial syndrome of 46,XY gonadal dysgenesis with anomalies of ectodermal and mesodermal structures.
    Brosnan PG, Lewandowski RC, Toguri AG, Payer AF, Meyer WJ.
    J Pediatr; 1980 Oct; 97(4):586-90. PubMed ID: 6158563
    [Abstract] [Full Text] [Related]

  • 6. Embryonic testicular regression sequence: a part of the clinical spectrum of 46,XY gonadal dysgenesis.
    Marcantonio SM, Fechner PY, Migeon CJ, Perlman EJ, Berkovitz GD.
    Am J Med Genet; 1994 Jan 01; 49(1):1-5. PubMed ID: 8172233
    [Abstract] [Full Text] [Related]

  • 7. Agonadism with positive H-Y antigen.
    Kinoshita K, Shiina Y, Bando M, Seino K, Yamada K.
    Clin Genet; 1984 Jul 01; 26(1):61-4. PubMed ID: 6467658
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  • 9. 45,X/46,XY mosaicism. A clinical review and report of ten cases.
    Knudtzon J, Aarskog D.
    Eur J Pediatr; 1987 May 01; 146(3):266-71. PubMed ID: 3595646
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  • 11. [Diagnosis and management of 46,XY mixed gonadal dysgenesis and disorder of sexual differentiation].
    Verkauskas G, Macianskyte D, Janciauskas D, Preiksa RT, Verkauskiene R, Jaubert F.
    Medicina (Kaunas); 2009 May 01; 45(5):357-64. PubMed ID: 19535881
    [Abstract] [Full Text] [Related]

  • 12. Low birth-weight, microcephalic malformation syndrome in a 46,XX girl and her 46,XY sister with agonadism: third report of the Kennerknecht syndrome or autosomal recessive Seckel-like syndrome with previously undescribed genital anomalies.
    Silengo M, Del Monaco A, Linari A, Lala R.
    Am J Med Genet; 2001 Jul 01; 101(3):275-8. PubMed ID: 11424145
    [Abstract] [Full Text] [Related]

  • 13. [The male 46,XY karyotype in a female phenotype].
    Luptáková Z, Baxová A, Hnilicová S, Durovcíková D, Dibarborová K, Dósová M, Karczubová M, Matúsková M.
    Bratisl Lek Listy; 1985 Jun 01; 83(6):605-19. PubMed ID: 4016550
    [No Abstract] [Full Text] [Related]

  • 14. [Study on familial 46, XY gonadal dysgenesis and high risk of gonadal tumors. III. Establishment of a fibroblast cell line (TGD-8F) on individual with 46, XY gonadal dysgenesis].
    E Z.
    Zhonghua Zhong Liu Za Zhi; 1983 Jan 01; 5(1):29-30. PubMed ID: 6851828
    [No Abstract] [Full Text] [Related]

  • 15. XY gonadal dysgenesis: genetic heterogeneity based upon clinical observations, H-Y antigen status and segregation analysis.
    Simpson JL, Blagowidow N, Martin AO.
    Hum Genet; 1981 Jan 01; 58(1):91-7. PubMed ID: 7286997
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  • 18. The X linked recessive form of XY gonadal dysgenesis with a high incidence of gonadal germ cell tumours: clinical and genetic studies.
    Mann JR, Corkery JJ, Fisher HJ, Cameron AH, Mayerová A, Wolf U, Kennaugh AA, Woolley V.
    J Med Genet; 1983 Aug 01; 20(4):264-70. PubMed ID: 6620326
    [Abstract] [Full Text] [Related]

  • 19. [Morphological characteristics indicating testicular differentiation in various forms of the streak-gonad syndrome].
    Gaál M, László J, Bösze P.
    Morphol Igazsagugyi Orv Sz; 1983 Jan 01; 23(1):41-7. PubMed ID: 6682481
    [No Abstract] [Full Text] [Related]

  • 20. [Swyer syndrome. Apropos of a new case of pure gonadal dysgenesis with Karyotype 46 XY].
    Cossard F, Saurel J, Berger-Pauquet M, Brun G.
    J Gynecol Obstet Biol Reprod (Paris); 1984 Jan 01; 13(2):151-6. PubMed ID: 6736590
    [Abstract] [Full Text] [Related]

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