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PUBMED FOR HANDHELDS

Journal Abstract Search

87 related items for PubMed ID: 2090119

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2. Autosomal recessive Robinow syndrome.
    Teebi AS.
    Am J Med Genet; 1990 Jan; 35(1):64-8. PubMed ID: 2301471
    [Abstract] [Full Text] [Related]

  • 3. A new autosomal recessive disorder resembling Weaver syndrome.
    Teebi AS, Sundareshan TS, Hammouri MY, al-Awadi SA, al-Saleh QA.
    Am J Med Genet; 1989 Aug; 33(4):479-82. PubMed ID: 2596508
    [Abstract] [Full Text] [Related]

  • 4. Multiple lentigines syndrome in a Nigerian family.
    Kubeyinje EP, Onunu AN, Obasohan AO.
    Trop Geogr Med; 1993 Aug; 45(3):135-7. PubMed ID: 8362457
    [Abstract] [Full Text] [Related]

  • 5. Roberts syndrome: study of 4 new Rgyptian cases with comparison of clinical and cytogenetic findings.
    Temtamy SA, Ismail S, Helmy NA.
    Genet Couns; 2006 Aug; 17(1):1-13. PubMed ID: 16719272
    [Abstract] [Full Text] [Related]

  • 6. Fallot complex, severe mental, and growth retardation: a new autosomal recessive syndrome?
    Bindewald B, Ulmer H, Müller U.
    Am J Med Genet; 1994 Apr 01; 50(2):173-6. PubMed ID: 8010348
    [Abstract] [Full Text] [Related]

  • 7. Phenotypic variability in children with growth hormone deficiency associated with posterior pituitary ectopia.
    Simon D, Hadjiathanasiou C, Garel C, Czernichow P, Léger J.
    Clin Endocrinol (Oxf); 2006 Apr 01; 64(4):416-22. PubMed ID: 16584514
    [Abstract] [Full Text] [Related]

  • 8. New autosomal recessive lethal disorder with polycystic kidneys type Potter I, characteristic face, microcephaly, brachymelia, and congenital heart defects.
    Gillessen-Kaesbach G, Meinecke P, Garrett C, Padberg BC, Rehder H, Passarge E.
    Am J Med Genet; 1993 Feb 15; 45(4):511-8. PubMed ID: 8465860
    [Abstract] [Full Text] [Related]

  • 9. Melnick-Needles syndrome: indication for an autosomal recessive form.
    ter Haar B, Hamel B, Hendriks J, de Jager J.
    Am J Med Genet; 1982 Dec 15; 13(4):469-77. PubMed ID: 7158646
    [Abstract] [Full Text] [Related]

  • 10. Geleophysic dysplasia: 7-year follow-up study of a patient with an intermediate form.
    Titomanlio L, Della Casa R, Lecora M, Farina V, Sebastio G, Andria G, Parenti G.
    Am J Med Genet; 1999 Sep 03; 86(1):82-5. PubMed ID: 10440835
    [Abstract] [Full Text] [Related]

  • 11. Brief clinical report: autosomal recessive anophthalmia with multiple congenital abnormalities--type Waardenburg.
    Richieri-Costa A, Gollop TR, Otto PG.
    Am J Med Genet; 1983 Apr 03; 14(4):607-15. PubMed ID: 6846395
    [Abstract] [Full Text] [Related]

  • 12. Probable autosomal recessive inheritance of polysplenia, situs inversus and cardiac defects in an Amish family.
    Arnold GL, Bixler D, Girod D.
    Am J Med Genet; 1983 Sep 03; 16(1):35-42. PubMed ID: 6638068
    [Abstract] [Full Text] [Related]

  • 13. Autosomal recessive mode of inheritance of a Coffin-Siris like syndrome.
    Bonioli E, Palmieri A, Bertola A, Bellini C.
    Genet Couns; 1995 Sep 03; 6(4):309-12. PubMed ID: 8775417
    [Abstract] [Full Text] [Related]

  • 14. [The lesions associated with leprechaunism (author's transl)].
    Lebreuil G, Pizzi M, Sebaoun M, Oddou JH.
    Arch Anat Cytol Pathol; 1980 Sep 03; 28(5):310-6. PubMed ID: 7447519
    [No Abstract] [Full Text] [Related]

  • 15. Frontofacionasal dysplasia: evidence for autosomal recessive inheritance.
    Gollop TR, Kiota MM, Martins RM, Lucchesi EA, Alvarenga Filho E.
    Am J Med Genet; 1984 Oct 03; 19(2):301-5. PubMed ID: 6439039
    [Abstract] [Full Text] [Related]

  • 16. Two siblings with midline field defects and Hirschsprung disease: variable expression of Toriello-Carey or new syndrome?
    Jespers A, Buntinx I, Melis K, Vaerenberg M, Janssens G.
    Am J Med Genet; 1993 Aug 15; 47(2):299-302. PubMed ID: 8213924
    [Abstract] [Full Text] [Related]

  • 17. Acrofacial dysplasia resembling geleophysic dysplasia.
    Spranger J, Gilbert EF, Flatz S, Burdelski M, Kallfelz HC.
    Am J Med Genet; 1984 Nov 15; 19(3):501-6. PubMed ID: 6507496
    [Abstract] [Full Text] [Related]

  • 18. Autosomal recessive congenital cerebellar hypoplasia and short stature in a large inbred family.
    Mégarbané A, Delague V, Salem N, Loiselet J.
    Am J Med Genet; 1999 Nov 05; 87(1):88-90. PubMed ID: 10528257
    [No Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20. Autosomal recessive deafness with skeletal dysplasia and facial appearance of Marshall syndrome.
    Miny P, Lenz W.
    Am J Med Genet; 1985 Jun 05; 21(2):317-24. PubMed ID: 4014313
    [Abstract] [Full Text] [Related]

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