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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

204 related items for PubMed ID: 9401100

  • 21.
    ; . PubMed ID:
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  • 22. [Floating-Harbor syndrome: first case in Italy associated with growth hormone deficiency].
    Femiano P, Castaldo V, Scarano G.
    Minerva Pediatr; 2000 Apr; 52(4):227-30. PubMed ID: 11995206
    [Abstract] [Full Text] [Related]

  • 23. Chiari I malformation as part of the Floating-Harbor syndrome?
    Kurzbuch AR, Magdum S.
    Eur J Med Genet; 2016 Dec; 59(12):615-617. PubMed ID: 27815143
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  • 24.
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  • 25. Pitt-Rogers-Danks syndrome: further delineation.
    Lizcano-Gil LA, García-Cruz D, García-Cruz O, Sánchez-Corona J.
    Am J Med Genet; 1995 Feb 13; 55(4):420-2. PubMed ID: 7762580
    [Abstract] [Full Text] [Related]

  • 26. Submicroscopic unbalanced translocation resulting in del10p/dup13q detected by subtelomere FISH.
    Roos A, Rudnik-Schöneborn S, Eggermann K, Eggermann T, Senderek J, Schwanitz G, Zerres K, Schüler HM.
    Eur J Med Genet; 2006 Feb 13; 49(6):505-10. PubMed ID: 16905374
    [Abstract] [Full Text] [Related]

  • 27. Smith-Fineman-Myers syndrome: report of a third case.
    Stephenson LD, Johnson JP.
    Am J Med Genet; 1985 Oct 13; 22(2):301-4. PubMed ID: 4050861
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  • 28.
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  • 29. The 4P-syndrome. Case description and literature review.
    Moretti P, Ferrari M, Di Battista S, Di Battista C.
    Minerva Pediatr; 2001 Feb 13; 53(1):23-8. PubMed ID: 11309539
    [Abstract] [Full Text] [Related]

  • 30. Report of a case and further delineation of the SHORT syndrome.
    Toriello HV, Wakefield S, Komar K, Higgins JV, Waterman DF.
    Am J Med Genet; 1985 Oct 13; 22(2):311-4. PubMed ID: 4050863
    [Abstract] [Full Text] [Related]

  • 31. [A case of Kabuki syndrome admitted for acute diarrhea and growth retardation in a French hospital in tropical area].
    Santiago J, Muszlak M, Goulois E, Ranaivoarivony V, Hébert JC, Lacombe D, Verloes A.
    Arch Pediatr; 2010 May 13; 17(5):588-93. PubMed ID: 20138485
    [Abstract] [Full Text] [Related]

  • 32. Café au lait macules and cerebro-oculo-facio-skeletal syndrome: a novel association.
    Twede JV, Difazio M.
    Pediatr Dermatol; 2009 May 13; 26(1):97-9. PubMed ID: 19250421
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  • 33.
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  • 34. [Seckel syndrome. Report of a case].
    Colli R, Russo F, Bianchi GA.
    Minerva Pediatr; 1995 Mar 13; 47(3):89-91. PubMed ID: 7791718
    [Abstract] [Full Text] [Related]

  • 35. Floating-Harbor Syndrome: report on a case in a mother and daughter, further evidence of autosomal dominant inheritance.
    Arpin S, Afenjar A, Dubern B, Toutain A, Cabrol S, Héron D.
    Clin Dysmorphol; 2012 Jan 13; 21(1):11-14. PubMed ID: 21955542
    [Abstract] [Full Text] [Related]

  • 36.
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  • 37.
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  • 38. GMS syndrome: a new dominant condition with goniodysgenesis, mental retardation, and short stature.
    Kupchik GS, Ludman MD, Raab EL, Gilbert F.
    Am J Med Genet; 1992 Jan 01; 42(1):1-4. PubMed ID: 1308345
    [Abstract] [Full Text] [Related]

  • 39. 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 01; 74(5):455-62. PubMed ID: 18651844
    [Abstract] [Full Text] [Related]

  • 40.
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