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Journal Abstract Search

164 related items for PubMed ID: 8685014

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  • 2. [Lethal osteo-chondro-dysplasia: feto-pathological study of 32 cases].
    Lahmar-Boufaroua A, Yacoubi MT, Hmisssa S, Selmi M, Korbi S.
    Tunis Med; 2009 Feb; 87(2):127-32. PubMed ID: 19522446
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  • 4. Multiple congenital anomalies associated with an oto-palato-digital syndrome type II.
    Blanchet P, Lefort G, Eglin MC, Rieu D, Sarda P.
    Genet Couns; 1993 Feb; 4(4):289-94. PubMed ID: 8110417
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  • 5. Patient with the mesomelic dysplasia, Nievergelt syndrome, and cerebellovermian agenesis and cataracts.
    Tüysüz B, Zeybek C, Zorer G, Sipahi O, Ungür S.
    Am J Med Genet; 2002 May 01; 109(3):206-10. PubMed ID: 11977180
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  • 6. Atelosteogenesis type I: autopsy findings.
    Wessels A, Wainwright HC, Beighton P.
    Pediatr Dev Pathol; 2011 May 01; 14(6):496-500. PubMed ID: 21985323
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  • 11. Pathological case of the month. Campomelic dysplasia.
    Iravani S, Debich-Spicer D, Gilbert-Barness E.
    Arch Pediatr Adolesc Med; 2000 Jul 01; 154(7):747-8. PubMed ID: 10891031
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  • 12. [Fatal genetic-morphologic syndromes. The campomelic syndrome].
    Henkel KE, Pfeiffer RA, Stöss H.
    Pathologe; 1993 May 01; 14(3):162-4. PubMed ID: 8516273
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  • 13. [Lethal chondrodysplasia with short ribs, Majewski type. Diagnosis in utero].
    Nivelon-Chevallier A, Halfon D, Mabille JP.
    Pediatrie; 1982 Sep 01; 37(6):453-9. PubMed ID: 7155726
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  • 14. Schwartz-Jampel syndrome: three pediatric case reports.
    Yapicioğlu H, Satar M, Yildizdaş D, Narli N, Suleymanova D, Tutak E.
    Genet Couns; 2003 Sep 01; 14(3):353-8. PubMed ID: 14577682
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  • 15. Achondrogenesis: a review with special consideration of achondrogenesis type II (Langer-Saldino).
    Chen H, Liu CT, Yang SS.
    Am J Med Genet; 1981 Sep 01; 10(4):379-94. PubMed ID: 7036745
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  • 16. Skeletal dysplasias: 38 prenatal cases.
    Witters I, Moerman P, Fryns JP.
    Genet Couns; 2008 Sep 01; 19(3):267-75. PubMed ID: 18990981
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  • 18. [Prenatal diagnosis of skeletal dysplasia: case report of a fetus with multiple anomalies].
    Novakov Mikić A, Stojić S, Konstantinidis G, Ristivojević A, Krnojelac D.
    Med Pregl; 2000 Sep 01; 53(3-4):197-201. PubMed ID: 10965689
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