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Journal Abstract Search

230 related items for PubMed ID: 3400727

  • 21. 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]

  • 22. Syndrome of mental retardation, facial anomalies, hypopituitarism, and distal arthrogryposis in sibs.
    Chitayat D, Hall JG, Couch RM, Phang MS, Baldwin VJ.
    Am J Med Genet; 1990 Sep 01; 37(1):65-70. PubMed ID: 2240046
    [Abstract] [Full Text] [Related]

  • 23. Apparently new autosomal recessive syndrome of mental retardation, distal limb deficiencies, oral involvement, and possible renal defect.
    Buttiens M, Fryns JP.
    Am J Med Genet; 1987 Jul 01; 27(3):651-60. PubMed ID: 3631136
    [Abstract] [Full Text] [Related]

  • 24. Japanese kindred with FG syndrome.
    Kato R, Niikawa N, Nagai T, Fukushima Y.
    Am J Med Genet; 1994 Aug 15; 52(2):242-3. PubMed ID: 7802020
    [No Abstract] [Full Text] [Related]

  • 25. An apparently new syndrome of microcephalic primordial dwarfism and cataracts.
    Toriello HV, Horton WA, Oostendorp A, Waterman DF, Higgins JV.
    Am J Med Genet; 1986 Sep 15; 25(1):1-8. PubMed ID: 3799711
    [Abstract] [Full Text] [Related]

  • 26. 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]

  • 27. 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 15; 2(4):317-21. PubMed ID: 8305962
    [Abstract] [Full Text] [Related]

  • 28. A new case of neonatal progeroid syndrome with agenesis of corpus callosum.
    Abdel-Salam GM, Czeizel AE.
    Genet Couns; 1999 Oct 15; 10(4):377-81. PubMed ID: 10631926
    [Abstract] [Full Text] [Related]

  • 29. Three sibs with phalangeal anomalies, microcephaly, severe mental retardation, and neurological abnormalities.
    Woods CG, Crouchman M, Huson SM.
    J Med Genet; 1992 Jul 15; 29(7):500-2. PubMed ID: 1640433
    [Abstract] [Full Text] [Related]

  • 30. Wrinkly skin syndrome: phenotype and additional manifestations.
    Casamassima AC, Wesson SK, Conlon CJ, Weiss FH.
    Am J Med Genet; 1987 Aug 15; 27(4):885-93. PubMed ID: 3321993
    [Abstract] [Full Text] [Related]

  • 31. 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 15; 16(4):475-80. PubMed ID: 6660246
    [Abstract] [Full Text] [Related]

  • 32. The Dubowitz syndrome.
    Wilroy RS, Tipton RE, Summitt RL.
    Am J Med Genet; 1978 Dec 15; 2(3):275-84. PubMed ID: 263660
    [Abstract] [Full Text] [Related]

  • 33. Cerebral abnormalities in the Neu-Laxova syndrome.
    Ostrovskaya TI, Lazjuk GI.
    Am J Med Genet; 1988 Jul 15; 30(3):747-56. PubMed ID: 3055985
    [Abstract] [Full Text] [Related]

  • 34. A syndrome of microcephaly, mental retardation, unusual facies, cleft palate, and weight deficiency.
    Weaver DD, Williams CP.
    Birth Defects Orig Artic Ser; 1977 Jul 15; 13(3B):69-84. PubMed ID: 890101
    [Abstract] [Full Text] [Related]

  • 35. 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 15; 34(4):593-600. PubMed ID: 2624276
    [Abstract] [Full Text] [Related]

  • 36. Dubowitz syndrome: a defect in the cholesterol biosynthetic pathway?
    Ahmad A, Amalfitano A, Chen YT, Kishnani PS, Miller C, Kelley R.
    Am J Med Genet; 1999 Oct 29; 86(5):503-4. PubMed ID: 10508998
    [No Abstract] [Full Text] [Related]

  • 37. Drayer's syndrome of mental retardation, microcephaly, short stature and absent phalanges is caused by a recurrent deletion of chromosome 15(q26.2-->qter).
    Rump P, Dijkhuizen T, Sikkema-Raddatz B, Lemmink HH, Vos YJ, Verheij JB, van Ravenswaaij CM.
    Clin Genet; 2008 Nov 29; 74(5):455-62. PubMed ID: 18651844
    [Abstract] [Full Text] [Related]

  • 38. Cleft palate-lateral synechiae syndrome: report on three new patients with additional findings and evidence for variability and heterogeneity.
    Nakata NM, Guion-Almeida ML, Richieri-Costa A.
    Am J Med Genet; 1993 Sep 01; 47(3):330-2. PubMed ID: 8135276
    [Abstract] [Full Text] [Related]

  • 39. New X-linked mental retardation (XLMR) syndrome with distinct facial appearance and growth retardation.
    Brooks SS, Wisniewski K, Brown WT.
    Am J Med Genet; 1994 Jul 15; 51(4):586-90. PubMed ID: 7943044
    [Abstract] [Full Text] [Related]

  • 40. Hallux duplication, postaxial polydactyly, absence of the corpus callosum, severe mental retardation, and additional anomalies in two unrelated patients: a new syndrome.
    Schinzel A, Schmid W.
    Am J Med Genet; 1980 Jul 15; 6(3):241-9. PubMed ID: 7424976
    [Abstract] [Full Text] [Related]

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