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Journal Abstract Search

141 related items for PubMed ID: 2077135

  • 1. Incest and mental handicap.
    Jancar J, Johnston SJ.
    J Ment Defic Res; 1990 Dec; 34 ( Pt 6)():483-90. PubMed ID: 2077135
    [Abstract] [Full Text] [Related]

  • 2. [Genetic risks of children of incestuous and consanguineous unions].
    Seemanová E.
    Z Arztl Fortbild (Jena); 1986 Dec; 80(19):799-802. PubMed ID: 3811414
    [No Abstract] [Full Text] [Related]

  • 3. A study of children of incestuous matings.
    Seemanová E.
    Hum Hered; 1971 Dec; 21(2):108-28. PubMed ID: 5127404
    [No Abstract] [Full Text] [Related]

  • 4. Primordial osteodysplastic dwarfism type I in association with corneal clouding: evidence for autosomal recessive inheritance.
    Van Maldergem L, Gillerot Y, Godhaird M, Nemec E, Koulischer L.
    Clin Genet; 1990 Nov; 38(5):359-61. PubMed ID: 2282715
    [Abstract] [Full Text] [Related]

  • 5. Xerodermic idiocy or De Sanctis Cacchione syndrome. A description of an 8-year-old patient with xeroderma pigmentosum, mental retardation, and dwarfism.
    Friedman A, Naveh Y, Haim S.
    Clin Pediatr (Phila); 1973 Jan; 12(1):56-8. PubMed ID: 4683062
    [No Abstract] [Full Text] [Related]

  • 6. The Dyggve-Melchior-Clausen syndrome in adult siblings.
    Bonafede RP, Beighton P.
    Clin Genet; 1978 Jul; 14(1):24-30. PubMed ID: 679519
    [Abstract] [Full Text] [Related]

  • 7. Genetic syndromes associated with cerebral palsy.
    Fisher RL, Russman BS.
    Clin Orthop Relat Res; 1974 Jul; (99):2-11. PubMed ID: 4825718
    [No Abstract] [Full Text] [Related]

  • 8. New autosomal recessive syndrome of mental retardation, epilepsy, short stature, and skeletal dysplasia.
    Gurrieri F, Sammito V, Bellussi A, Neri G.
    Am J Med Genet; 1992 Oct 01; 44(3):315-20. PubMed ID: 1488978
    [No Abstract] [Full Text] [Related]

  • 9. Children of incest.
    Baird PA, McGillivray B.
    J Pediatr; 1982 Nov 01; 101(5):854-7. PubMed ID: 7131177
    [Abstract] [Full Text] [Related]

  • 10. Osteodysplastic variant of primordial dwarfism.
    Shebib S, Hugosson C, Sakati N, Nyhan WL.
    Am J Med Genet; 1991 Aug 01; 40(2):146-50. PubMed ID: 1897566
    [Abstract] [Full Text] [Related]

  • 11. Recurrence risks in severe undiagnosed mental deficiency.
    Bundey S, Carter CO.
    J Ment Defic Res; 1974 Jun 01; 18(2):115-34. PubMed ID: 4475697
    [No Abstract] [Full Text] [Related]

  • 12. An autosomal recessive form of spastic cerebral palsy (CP) with microcephaly and mental retardation.
    Rajab A, Yoo SY, Abdulgalil A, Kathiri S, Ahmed R, Mochida GH, Bodell A, Barkovich AJ, Walsh CA.
    Am J Med Genet A; 2006 Jul 15; 140(14):1504-10. PubMed ID: 16761294
    [Abstract] [Full Text] [Related]

  • 13. Oto-palato-digital syndrome: comparison of clinical and radiographic manifestations in males and females.
    Gall JC, Stern AM, Poznanski AK, Garn SM, Weinstein ED, Hayward JR.
    Am J Hum Genet; 1972 Jan 15; 24(1):24-36. PubMed ID: 5012690
    [No Abstract] [Full Text] [Related]

  • 14. Autosomal recessive microcephaly with severe psychomotor retardation.
    Scheffer IE, Baraitser M, Wilson J, Godfrey C, Brett EM.
    Neuropediatrics; 1992 Feb 15; 23(1):53-6. PubMed ID: 1565220
    [Abstract] [Full Text] [Related]

  • 15. Telomeric tandem translocation tan (14; 15) (q32; q26) and absence of IgA in an incestuous child.
    Koulischer L, Lambotte C.
    Ann Genet; 1974 Sep 15; 17(3):189-92. PubMed ID: 4548820
    [No Abstract] [Full Text] [Related]

  • 16. Rhombencephalosynapsis with facial anomalies and probable autosomal recessive inheritance: a case report.
    Romanengo M, Tortori-Donati P, Di Rocco M.
    Clin Genet; 1997 Sep 15; 52(3):184-6. PubMed ID: 9377810
    [Abstract] [Full Text] [Related]

  • 17. Partial monosomy of 7q32 in a case of de novo rcp(7;15)(q32;q15).
    D'Alessandro E, Ligas C, Lo Re ML, Marcanio MP, Gentile T, Del Porto G.
    J Med Genet; 1994 May 15; 31(5):413-5. PubMed ID: 8064823
    [Abstract] [Full Text] [Related]

  • 18. New autosomal recessive syndrome of mental retardation, coarse face, microcephaly, epilepsy and skeletal abnormalities.
    Battaglia A, Ferrari AR, Orsitto E, Gibilisco G, Neri G.
    Clin Dysmorphol; 1996 Jan 15; 5(1):41-7. PubMed ID: 8867658
    [Abstract] [Full Text] [Related]

  • 19. Johanson-Blizzard syndrome in a large inbred kindred with three involved members.
    Mardini MK, Ghandour M, Sakati NA, Nyhan WL.
    Clin Genet; 1978 Nov 15; 14(5):247-50. PubMed ID: 709902
    [Abstract] [Full Text] [Related]

  • 20. [Dyggve-Melchior-Clausen dysplasia (apropos of a case)].
    Sbihi A, Benharbit R, Lahrichi A, Lahrech MT.
    Maghrib Tibbi; 1980 Dec 15; 2(4):367-74. PubMed ID: 7345231
    [No Abstract] [Full Text] [Related]

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