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Journal Abstract Search

98 related items for PubMed ID: 1112852

  • 21. Michelin tire baby syndrome: familial constriction bands during infancy and early childhood in four generations.
    Bass HN, Caldwell S, Brooks BS.
    Am J Med Genet; 1993 Feb 01; 45(3):370-2. PubMed ID: 8434626
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  • 23. Omphalocele in three generations with autosomal dominant transmission.
    Kanagawa SL, Begleiter ML, Ostlie DJ, Holcomb G, Drake W, Butler MG.
    J Med Genet; 2002 Mar 01; 39(3):184-5. PubMed ID: 11897819
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  • 24. Dominant inheritance in two families with familial Mediterranean fever (FMF).
    Yuval Y, Hemo-Zisser M, Zemer D, Sohar E, Pras M.
    Am J Med Genet; 1995 Jul 03; 57(3):455-7. PubMed ID: 7677151
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  • 25. Congenital hypoplastic anemia: another example of autosomal dominant transmission.
    Gojic V, van't Veer-Korthof ET, Bosch LJ, Puyn WH, van Haeringen A.
    Am J Med Genet; 1994 Mar 01; 50(1):87-9. PubMed ID: 8160759
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  • 26. Autosomal dominant isolated ('uncomplicated') microcephaly.
    Merlob P, Steier D, Reisner SH.
    J Med Genet; 1988 Nov 01; 25(11):750-3. PubMed ID: 3236353
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  • 32. Syndrome of tibial hypoplasia with polydactyly-syndactyly in two generations.
    Karamitsos S, Bartsocas CS.
    Prog Clin Biol Res; 1982 Nov 01; 104():289-97. PubMed ID: 6298813
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  • 34. Familial infantile cortical hyperostosis in a large Canadian family.
    Maclachlan AK, Gerrard JW, Houston CS, Ives EJ.
    Can Med Assoc J; 1984 May 01; 130(9):1172-4. PubMed ID: 6370402
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  • 35. Kyphomelic dysplasia: a report of a family with an autosomal dominant pattern.
    Toledo C, Navarro-Barros R, Alba L, Muñoz E.
    Ann Genet; 1999 May 01; 42(3):170-3. PubMed ID: 10526661
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  • 36. Radial meromelia. The deformity and its treatment.
    Bora FW, Nicholson JT, Cheema HM.
    J Bone Joint Surg Am; 1970 Jul 01; 52(5):966-79. PubMed ID: 5479484
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  • 38. Familial hyperproinsulinemia. An autosomal dominant defect.
    Gabbay KH, DeLuca K, Fisher JN, Mako ME, Rubenstein AH.
    N Engl J Med; 1976 Apr 22; 294(17):911-5. PubMed ID: 815812
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  • 39. A complex deformity of appendicular skeleton and shoulder with congenital heart disease in three generations of a Jordanian family.
    Boehme DH, Shotar AO.
    Clin Genet; 1989 Dec 22; 36(6):442-50. PubMed ID: 2591070
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