These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

278 related items for PubMed ID: 1227520

  • 1. Probable Marden-Walker syndrome: evidence for autosomal recessive inheritance.
    Temtamy SA, Shoukry AS, Raafat M, Mihareb S.
    Birth Defects Orig Artic Ser; 1975; 11(2):104-8. PubMed ID: 1227520
    [Abstract] [Full Text] [Related]

  • 2. Marden-Walker syndrome: a case report and a critical review of the literature.
    Williams MS, Josephson KD, Wargowski DS.
    Clin Dysmorphol; 1993 Jul; 2(3):211-9. PubMed ID: 7506965
    [Abstract] [Full Text] [Related]

  • 3. Marden-Walker syndrome: case report, nosologic discussion and aspects of counseling.
    Garavelli L, Donadio A, Banchini G, Magnani C, Magnani C, Calzolari E, Fryns JP.
    Genet Couns; 2000 Jul; 11(2):111-8. PubMed ID: 10893662
    [Abstract] [Full Text] [Related]

  • 4. Congenital myopathy with oculo-facial abnormalities (Marden-Walker syndrome).
    Linder N, Mathot I, Livoff A, Glass J, Bornstein I, Gross E, Yatsiv S, Sommer A.
    Am J Med Genet; 1991 Jun 15; 39(4):377-9. PubMed ID: 1877612
    [Abstract] [Full Text] [Related]

  • 5. Marden-Walker phenotype: a diagnostic dilemma.
    Soekarman D, Volcke P, Legius E, Holvoet M, Fryns JP.
    Genet Couns; 1996 Jun 15; 7(1):31-9. PubMed ID: 8652086
    [Abstract] [Full Text] [Related]

  • 6. Marden-Walker-like syndrome without psychomotor retardation: report of a Brazilian girl born to consanguineous parents.
    van den Ende JJ, van Bever Y, Rodini ES, Richieri-Costa A.
    Am J Med Genet; 1992 Feb 15; 42(4):467-9. PubMed ID: 1609830
    [Abstract] [Full Text] [Related]

  • 7. Brief clinical report and review: the Marden-Walker syndrome.
    Jaatoul NY, Haddad NE, Khoury LA, Afifi AK, Bahuth NB, Deeb ME, Mikati MA, Der Kaloustian VM.
    Am J Med Genet; 1982 Mar 15; 11(3):259-71. PubMed ID: 7081292
    [Abstract] [Full Text] [Related]

  • 8. 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]

  • 9. Autosomal recessive mode of inheritance of a Coffin-Siris like syndrome.
    Bonioli E, Palmieri A, Bertola A, Bellini C.
    Genet Couns; 1995 Apr 01; 6(4):309-12. PubMed ID: 8775417
    [Abstract] [Full Text] [Related]

  • 10. [Marden-Walker syndrome--a case report].
    Dumić M, Rojnić-Putarek N, Skrablin-Kucić S, Matić T, Ille J, Radica A.
    Lijec Vjesn; 2009 Apr 01; 131(7-8):203-6. PubMed ID: 19769282
    [Abstract] [Full Text] [Related]

  • 11. [Craniofacial dysmorphism with flexion of the fingers. Marden-Walker syndrome?].
    Kubryk N, Borde M.
    Sem Hop; 1982 Nov 11; 58(41):2405-7. PubMed ID: 6297028
    [Abstract] [Full Text] [Related]

  • 12. Short stature, Robin sequence, cleft mandible, pre/postaxial hand anomalies, and clubfoot: a new autosomal recessive syndrome.
    Richieri-Costa A, Pereira SC.
    Am J Med Genet; 1992 Mar 01; 42(5):681-7. PubMed ID: 1632438
    [Abstract] [Full Text] [Related]

  • 13. Autosomal recessive ectodermal dysplasia, cleft lip/palate, mental retardation, and syndactyly: the Zlotogora-Ogur syndrome.
    Rodini ES, Richieri-Costa A.
    Am J Med Genet; 1990 Aug 01; 36(4):473-6. PubMed ID: 2167611
    [Abstract] [Full Text] [Related]

  • 14. Marden-Walker syndrome in an adult.
    Kotzot D, Schinzel A.
    Clin Dysmorphol; 1995 Jul 01; 4(3):260-5. PubMed ID: 7551165
    [Abstract] [Full Text] [Related]

  • 15. Hutterite cerebro-osteo-nephrodysplasia: autosomal recessive trait in a Lehrerleut Hutterite family from Montana.
    Opitz JM, Lowry RB, Holmes TM, Morgan K.
    Am J Med Genet; 1985 Nov 01; 22(3):521-9. PubMed ID: 4061488
    [Abstract] [Full Text] [Related]

  • 16. A previously undescribed autosomal recessive multiple congenital anomalies/mental retardation (MCA/MR) syndrome with growth failure, lip/palate cleft(s), and urogenital anomalies.
    Malpuech G, Demeocq F, Palcoux JB, Vanlieferinghen P.
    Am J Med Genet; 1983 Dec 01; 16(4):475-80. PubMed ID: 6660246
    [Abstract] [Full Text] [Related]

  • 17. Peters'-Plus syndrome with agenesis of the corpus callosum: report of a case and confirmation of autosomal recessive inheritance.
    Camera G, Centa A, Pozzolo S, Camera A.
    Clin Dysmorphol; 1993 Oct 01; 2(4):317-21. PubMed ID: 8305962
    [Abstract] [Full Text] [Related]

  • 18. [Spondylo-epiphyseal dysplasia associated with craniosynostosis, cleft palate and mental retardation. A case report].
    Herrera-Martínez AD, Estrada-Corona P.
    Invest Clin; 2010 Dec 01; 51(4):553-60. PubMed ID: 21365879
    [Abstract] [Full Text] [Related]

  • 19. [Marden-Walker syndrome].
    Imaizumi K.
    Ryoikibetsu Shokogun Shirizu; 2000 Dec 01; (30 Pt 5):15-7. PubMed ID: 11057127
    [No Abstract] [Full Text] [Related]

  • 20. Autosomal recessive intestinal lymphangiectasia and lymphedema, with facial anomalies and mental retardation.
    Hennekam RC, Geerdink RA, Hamel BC, Hennekam FA, Kraus P, Rammeloo JA, Tillemans AA.
    Am J Med Genet; 1989 Dec 01; 34(4):593-600. PubMed ID: 2624276
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 14.