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Journal Abstract Search

305 related items for PubMed ID: 10874634

  • 1. Complex consanguinity associated with short rib-polydactyly syndrome III and congenital infection-like syndrome: a diagnostic problem in dysmorphic syndromes.
    al-Gazali LI, Sztriha L, Dawodu A, Varady E, Bakir M, Khdir A, Johansen J.
    J Med Genet; 1999 Jun; 36(6):461-6. PubMed ID: 10874634
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  • 2. Diagnostic dilemmas in the short rib-polydactyly syndrome group.
    Elçioglu NH, Hall CM.
    Am J Med Genet; 2002 Sep 01; 111(4):392-400. PubMed ID: 12210298
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  • 3. A new short rib syndrome: report of two cases.
    Beemer FA, Langer LO, Klep-de Pater JM, Hemmes AM, Bylsma JB, Pauli RM, Myers TL, Haws CC.
    Am J Med Genet; 1983 Jan 01; 14(1):115-23. PubMed ID: 6829599
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  • 4. Short rib-dysplasia group (with/without polydactyly): report of a patient suggesting the existence of a continuous spectrum.
    Franceschini P, Guala A, Vardeu MP, Signorile F, Franceschini D, Bolgiani MP.
    Am J Med Genet; 1995 Nov 20; 59(3):359-64. PubMed ID: 8599362
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  • 5. Calcospherite (calcification nodule) size in the short rib polydactyly syndromes.
    Gruber HE, Lachman RS, Rimoin DL.
    Scanning Microsc; 1990 Sep 20; 4(3):775-80. PubMed ID: 2080437
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  • 8. Short rib syndrome Beemer-Langer type with polydactyly: a multiple congenital anomalies syndrome.
    Yang SS, Roth JA, Langer LO.
    Am J Med Genet; 1991 Jun 01; 39(3):243-6. PubMed ID: 1867272
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  • 14. Brief clinical report: autosomal recessive anophthalmia with multiple congenital abnormalities--type Waardenburg.
    Richieri-Costa A, Gollop TR, Otto PG.
    Am J Med Genet; 1983 Apr 01; 14(4):607-15. PubMed ID: 6846395
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  • 15. Recurrent short rib polydactyly syndrome.
    Eleftheriades M, Iavazzo C, Manolakos E, Hassiakos D, Botsis D, Petersen M, Konstantinidou A.
    J Obstet Gynaecol; 2013 Jan 01; 33(1):14-6. PubMed ID: 23259870
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  • 16. Overlap between Majewski and hydrolethalus syndromes: a report of two cases.
    Sharma AK, Phadke S, Chandra K, Upreti M, Khan EM, Naveed M, Agarwal SS.
    Am J Med Genet; 1992 Aug 01; 43(6):949-53. PubMed ID: 1415345
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  • 17. Clinical and genetic heterogeneity of Seckel syndrome.
    Faivre L, Le Merrer M, Lyonnet S, Plauchu H, Dagoneau N, Campos-Xavier AB, Attia-Sobol J, Verloes A, Munnich A, Cormier-Daire V.
    Am J Med Genet; 2002 Nov 01; 112(4):379-83. PubMed ID: 12376940
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  • 18. Exclusion of the Ellis-van Creveld region on chromosome 4p16 in some families with asphyxiating thoracic dystrophy and short-rib polydactyly syndromes.
    Krakow D, Salazar D, Wilcox WR, Rimoin DL, Cohn DH.
    Eur J Hum Genet; 2000 Aug 01; 8(8):645-8. PubMed ID: 10951528
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  • 19. Short rib-polydactyly syndrome: a single or heterogeneous entity? A re-evaluation prompted by four new cases.
    Bernstein R, Isdale J, Pinto M, Du Toit Zaaijman J, Jenkins T.
    J Med Genet; 1985 Feb 01; 22(1):46-53. PubMed ID: 3981580
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