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

141 related items for PubMed ID: 1770530

  • 21. The Coffin-Lowry syndrome. A study of two new index patients and their families.
    Haspeslagh M, Fryns JP, Beusen L, Van Dessel F, Vinken L, Moens E, Van den Berghe H.
    Eur J Pediatr; 1984 Dec; 143(2):82-6. PubMed ID: 6519116
    [Abstract] [Full Text] [Related]

  • 22. X-linked mental retardation with bilateral clasped thumbs: report of another affected family.
    Straussberg R, Blatt I, Brand N, Kessler D, Katznelson MB, Goodman RM.
    Clin Genet; 1991 Nov; 40(5):337-41. PubMed ID: 1756607
    [Abstract] [Full Text] [Related]

  • 23. X-linked alpha-thalassemia/mental retardation (ATR-X) syndrome: localization to Xq12-q21.31 by X inactivation and linkage analysis.
    Gibbons RJ, Suthers GK, Wilkie AO, Buckle VJ, Higgs DR.
    Am J Hum Genet; 1992 Nov; 51(5):1136-49. PubMed ID: 1415255
    [Abstract] [Full Text] [Related]

  • 24. X-linked intellectual handicap and precocious puberty with obesity in carrier females.
    Hockey A.
    Am J Med Genet; 1986 Nov; 23(1-2):127-37. PubMed ID: 3953642
    [Abstract] [Full Text] [Related]

  • 25. A new X-linked mental retardation syndrome.
    Homfray T, Holland T, Patton M.
    Clin Dysmorphol; 1995 Oct; 4(4):289-93. PubMed ID: 8574418
    [Abstract] [Full Text] [Related]

  • 26. [Alpha-thalassemia/mental retardation syndrome (ATR-X) in two brothers - clinical characteristics, diagnostics and genetic counselling issues].
    Szczałuba K, Obersztyn E, Nowakowska B, Bernaciak J, Fisher C, Gibbons R, Mazurczak T, Bocian E.
    Med Wieku Rozwoj; 2011 Oct; 15(4):437-44. PubMed ID: 22516698
    [Abstract] [Full Text] [Related]

  • 27. [Three Japanese children with X-linked alpha-thalassemia/mental retardation syndrome (ATR-X)].
    Wada T, Nakamura M, Matsushita Y, Yamada M, Yamashita S, Iwamoto H, Masuno M, Imaizumi K, Kuroki Y.
    No To Hattatsu; 1998 Jul; 30(4):283-9. PubMed ID: 9695621
    [Abstract] [Full Text] [Related]

  • 28. Arch fingerprints, hypotonia, and areflexia associated with X linked mental retardation.
    Stevenson RE, Häne B, Arena JF, May M, Lawrence L, Lubs HA, Schwartz CE.
    J Med Genet; 1997 Jun; 34(6):465-9. PubMed ID: 9192265
    [Abstract] [Full Text] [Related]

  • 29. X-linked mental retardation associated with psoriasis: a new syndrome?
    Tranebjaerg L, Svejgaard A, Lykkesfeldt G.
    Am J Med Genet; 1988 Jun; 30(1-2):263-73. PubMed ID: 3177453
    [Abstract] [Full Text] [Related]

  • 30. Clinical features and molecular analysis of the alpha thalassemia/mental retardation syndromes. II. Cases without detectable abnormality of the alpha globin complex.
    Wilkie AO, Zeitlin HC, Lindenbaum RH, Buckle VJ, Fischel-Ghodsian N, Chui DH, Gardner-Medwin D, MacGillivray MH, Weatherall DJ, Higgs DR.
    Am J Hum Genet; 1990 Jun; 46(6):1127-40. PubMed ID: 2339705
    [Abstract] [Full Text] [Related]

  • 31. X-linked mental retardation and characteristic physical features in two brothers with duplication Xp22-Xpter.
    Cianchetti C, Muntoni F, Falchi AM, Nucaro A, Sannio-Fancello G, Cao A, Marrosu MG.
    Am J Med Genet; 1990 Jun; 43(1-2):475-8. PubMed ID: 1605229
    [Abstract] [Full Text] [Related]

  • 32. X-linked mental retardation with dystonic movements of the hands.
    Partington MW, Mulley JC, Sutherland GR, Hockey A, Thode A, Turner G.
    Am J Med Genet; 1988 Jun; 30(1-2):251-62. PubMed ID: 3177452
    [Abstract] [Full Text] [Related]

  • 33. British type alpha 0-thalassaemia in New Zealand.
    Trent RJ, Yakas J, Rutherford J, Blacklock HA, Mickleson KN.
    N Z Med J; 1989 Feb 08; 102(861):39-41. PubMed ID: 2739965
    [Abstract] [Full Text] [Related]

  • 34. Inherited microdeletion in Xp21.3-22.1 involved in non-specific mental retardation.
    des Portes V, Carrié A, Billuart P, Kieffer V, Bienvenu T, Vinet MC, Beldjord C, Kahn A, Ponsot G, Chelly J, Moutard ML.
    Clin Genet; 1998 Feb 08; 53(2):136-41. PubMed ID: 9611075
    [Abstract] [Full Text] [Related]

  • 35. The FG syndrome: 7 new cases.
    Thompson EM, Baraitser M, Lindenbaum RH, Zaidi ZH, Kroll JS.
    Clin Genet; 1985 Jun 08; 27(6):582-94. PubMed ID: 4017279
    [Abstract] [Full Text] [Related]

  • 36. MASA syndrome: delineation of the clinical spectrum at prepubertal age.
    Fryns JP, Schrander-Stumpel C, De Die-Smulders C, Borghgraef M, Van den Berghe H.
    Am J Med Genet; 1985 Jun 08; 43(1-2):402-7. PubMed ID: 1605218
    [Abstract] [Full Text] [Related]

  • 37. New XLMR syndrome with characteristic face, hypogenitalism, congenital hypotonia and pachygyria.
    Zollino M, Mastroiacovo P, Zampino G, Mariotti P, Neri G.
    Am J Med Genet; 1985 Jun 08; 43(1-2):452-7. PubMed ID: 1605225
    [Abstract] [Full Text] [Related]

  • 38. New X-linked syndrome with seizures, acquired micrencephaly, and agenesis of the corpus callosum.
    Proud VK, Levine C, Carpenter NJ.
    Am J Med Genet; 1985 Jun 08; 43(1-2):458-66. PubMed ID: 1605226
    [Abstract] [Full Text] [Related]

  • 39. Updating the N syndrome: occurrence of lymphoid malignancy and possible association with an increased rate of chromosome breakage.
    Hess RO, Hafez GR, Meisner LF.
    Am J Med Genet Suppl; 1987 Jun 08; 3():383-8. PubMed ID: 3130873
    [Abstract] [Full Text] [Related]

  • 40. The haemoglobin H disease mental retardation syndrome: molecular studies on the South African case.
    Bowcock AM, van Tonder S, Jenkins T.
    Br J Haematol; 1984 Jan 08; 56(1):69-78. PubMed ID: 6704328
    [Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 8.