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Journal Abstract Search

341 related items for PubMed ID: 6622139

  • 21. Childhood Autism in a female with Coffin Siris Syndrome.
    Hersh JH, Bloom AS, Weisskopf B.
    J Dev Behav Pediatr; 1982 Dec; 3(4):249-52. PubMed ID: 7153373
    [No Abstract] [Full Text] [Related]

  • 22. Unusual facial appearance, microcephaly, growth and mental retardation, and syndactyly. A new syndrome?
    Filippi G.
    Am J Med Genet; 1985 Dec; 22(4):821-4. PubMed ID: 4073130
    [Abstract] [Full Text] [Related]

  • 23. Severe mental retardation and absent nails of hallux and pollex.
    Temple IK, Baraitser M.
    Am J Med Genet; 1991 Nov 01; 41(2):173-5. PubMed ID: 1785628
    [No Abstract] [Full Text] [Related]

  • 24. Fryns syndrome phenotype and trisomy 22.
    Ladonne JM, Gaillard D, Carré-Pigeon F, Gabriel R.
    Am J Med Genet; 1996 Jan 02; 61(1):68-70. PubMed ID: 8741922
    [Abstract] [Full Text] [Related]

  • 25. [Familial syndrome of microcephaly with oculocutaneous albinism and digital anomalies].
    Castro-Gago M, Pombo M, Novo I, Tojo R, Peña J.
    An Esp Pediatr; 1983 Aug 02; 19(2):128-31. PubMed ID: 6660641
    [Abstract] [Full Text] [Related]

  • 26. Triplets with growth failure, microcephaly, mental retardation, nail hypoplasia and corpus callosum agenesis: is it a variant of Coffin-Siris or a new syndrome?
    Kirel B, Kural N, Yakut A, Adapinar B.
    Turk J Pediatr; 2000 Aug 02; 42(2):171-6. PubMed ID: 10936989
    [Abstract] [Full Text] [Related]

  • 27. [Orofaciodigital syndrome. Apropos of an 11th case in the same family].
    Vissian L, Vaillaud JC.
    Ann Dermatol Syphiligr (Paris); 1972 Aug 02; 99(1):5-20. PubMed ID: 5053179
    [No Abstract] [Full Text] [Related]

  • 28. Autosomal recessive mode of inheritance of a Coffin-Siris like syndrome.
    Bonioli E, Palmieri A, Bertola A, Bellini C.
    Genet Couns; 1995 Aug 02; 6(4):309-12. PubMed ID: 8775417
    [Abstract] [Full Text] [Related]

  • 29. [Onychoheterotopia with polyonychia associated with Pierre Robin syndrome: apropos of a new case. (Trial of classifying nail ectopia)].
    Roger H, Souteyrand P, Collin JP, Vanneuville G, Teinturier P.
    Ann Dermatol Venereol; 1986 Aug 02; 113(3):235-42. PubMed ID: 3752862
    [Abstract] [Full Text] [Related]

  • 30. The Coffin-Siris syndrome.
    Tunnessen WW, McMillan JA, Levin MB.
    Am J Dis Child; 1978 Apr 02; 132(4):393-5. PubMed ID: 645658
    [Abstract] [Full Text] [Related]

  • 31. Medulloblastoma in association with the Coffin-Siris syndrome.
    Rogers L, Pattisapu J, Smith RR, Parker P.
    Childs Nerv Syst; 1988 Feb 02; 4(1):41-4. PubMed ID: 2456854
    [Abstract] [Full Text] [Related]

  • 32. Hypoglycemia in Coffin-Siris syndrome.
    Imaizumi K, Nakamura M, Masuno M, Makita Y, Kuroki Y.
    Am J Med Genet; 1995 Oct 23; 59(1):49-50. PubMed ID: 8849011
    [Abstract] [Full Text] [Related]

  • 33. [Anesthesia for a pediatric patient with Coffin-Siris syndrome].
    Shirakami G, Tazuke-Nishimura M, Hirakata H, Fukuda K.
    Masui; 2005 Jan 23; 54(1):42-5. PubMed ID: 15717467
    [Abstract] [Full Text] [Related]

  • 34. Microcephaly and digital anomalies: a newly recognized syndrome of recessively inherited mental retardation.
    Kelly TE, Kirson L, Wyatt J.
    Am J Med Genet; 1993 Feb 01; 45(3):353-5. PubMed ID: 8434622
    [Abstract] [Full Text] [Related]

  • 35. Rubinstein-Taybi syndrome.
    Gellis SS, Feingold M.
    Am J Dis Child; 1971 Apr 01; 121(4):327-8. PubMed ID: 5550739
    [No Abstract] [Full Text] [Related]

  • 36. Two sisters with growth failure, microcephaly, peculiar facies and apical dystrophy: the presentation of brachymorphism-onychodysplasia-dysphalangism syndrome?
    Ounap K, Justus I, Lipping-Sitska M.
    Clin Dysmorphol; 1998 Jan 01; 7(1):45-50. PubMed ID: 9546830
    [Abstract] [Full Text] [Related]

  • 37. [The Williams and Beuren syndrome: aspects of the elfin facies].
    Bezzi TM, Bergamini M, Scorrano M, Pinca A.
    Pediatria (Napoli); 1983 Jan 01; 91(2-3):281-6. PubMed ID: 6664736
    [No Abstract] [Full Text] [Related]

  • 38. Three sibs with phalangeal anomalies, microcephaly, severe mental retardation, and neurological abnormalities.
    Woods CG, Crouchman M, Huson SM.
    J Med Genet; 1992 Jul 01; 29(7):500-2. PubMed ID: 1640433
    [Abstract] [Full Text] [Related]

  • 39. The craniodigital syndrome of Scott: report of a second family.
    Lorenz P, Hinkel GK, Hoffmann C, Rupprecht E.
    Am J Med Genet; 1990 Oct 01; 37(2):224-6. PubMed ID: 2174209
    [Abstract] [Full Text] [Related]

  • 40. Distinct phenotype of PHF6 deletions in females.
    Di Donato N, Isidor B, Lopez Cazaux S, Le Caignec C, Klink B, Kraus C, Schrock E, Hackmann K.
    Eur J Med Genet; 2014 Feb 01; 57(2-3):85-9. PubMed ID: 24380767
    [Abstract] [Full Text] [Related]

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