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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

163 related items for PubMed ID: 3425635

  • 21. [Autosomal recessive spondylometaphyseal dysplasia. Apropos of 3 familial cases].
    Meziane AO, Meziane A, Ksiyer M, Bennani-Smires C, Khalifa HH.
    Ann Genet; 1987; 30(4):216-20. PubMed ID: 3501265
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  • 22. Hand pattern profile analysis (HPPA): a new diagnostic tool.
    Hayes M, Say B.
    Clin Pediatr (Phila); 1977 Nov; 16(11):988-91. PubMed ID: 913014
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  • 25. Metacarpophalangeal pattern profile analysis in fragile X syndrome.
    Butler MG, Fletcher M, Gale DD, Meaney FJ, McLeod DR, Fagan J, Carpenter NJ.
    Am J Med Genet; 1988 Dec; 31(4):767-73. PubMed ID: 3239565
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  • 31. Acromesomelic dysplasia.
    Langer LO, Garrett RT.
    Radiology; 1980 Nov; 137(2):349-55. PubMed ID: 7433666
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  • 33. [Clinico-genetic analysis of multiple epiphyseal dysplasia].
    Meerson EM, Nechvolodova OL, Iukina GP, Bruskina VIa.
    Ortop Travmatol Protez; 1985 Dec; (12):13-7. PubMed ID: 4094735
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  • 35. Metacarpophalangeal pattern profile and bone age in Rett syndrome: further radiological clues to the diagnosis.
    Leonard H, Thomson M, Glasson E, Fyfe S, Leonard S, Ellaway C, Christodoulou J, Bower C.
    Am J Med Genet; 1999 Mar 12; 83(2):88-95. PubMed ID: 10190478
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  • 36. Metacarpophalangeal pattern profile analysis in 14 Japanese children with Sotos syndrome.
    Takahashi Y, Imaizumi K, Takada F, Kuroki Y.
    Jpn J Hum Genet; 1994 Mar 12; 39(1):187-91. PubMed ID: 8025295
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  • 37. Autosomal recessive omodysplasia: report of three additional cases.
    Masel JP, Kozlowski K, Kiss P.
    Pediatr Radiol; 1998 Aug 12; 28(8):608-11. PubMed ID: 9716634
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  • 38. A compound heterozygote of novel and recurrent DTDST mutations results in a novel intermediate phenotype of Desbuquois dysplasia, diastrophic dysplasia, and recessive form of multiple epiphyseal dysplasia.
    Miyake A, Nishimura G, Futami T, Ohashi H, Chiba K, Toyama Y, Furuichi T, Ikegawa S.
    J Hum Genet; 2008 Aug 12; 53(8):764-768. PubMed ID: 18553123
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  • 39. Surviving campomelic dysplasia has the radiological features of the previously reported ischio-pubic-patella syndrome.
    Offiah AC, Mansour S, McDowall S, Tolmie J, Sim P, Hall CM.
    J Med Genet; 2002 Sep 12; 39(9):e50. PubMed ID: 12205120
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  • 40. CODAS syndrome: a new distinct MCA/MR syndrome with radiological changes of spondyloepiphyseal dysplasia. Another case report.
    de Almeida JC, Vargas FR, Barbosa-Neto JG, Llerena JC.
    Am J Med Genet; 1995 Jan 02; 55(1):19-20. PubMed ID: 7702089
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