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PUBMED FOR HANDHELDS

Journal Abstract Search


115 related items for PubMed ID: 5802844

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  • 3. Familial transmission of a presumptive D/E (13-15/17-18) short arm translocation.
    Cohen MM, Lockwood MA.
    Pediatr Res; 1967 Mar; 1(2):104-9. PubMed ID: 6029809
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  • 4. Congenital heart disease in an infant with the Smith-Lemli-Opitz syndrome.
    Park SC, Needles CF, Dimich I, Sussman L.
    J Pediatr; 1968 Dec; 73(6):896-902. PubMed ID: 4386913
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  • 5. [Two malformative syndromes possibly unifiable: Ullrich-Feichtiger and Smith-Lemli-Opitz syndromes. Case report].
    Lendvai D, Castello MA, Ballati G.
    Minerva Pediatr; 1969 Jan 14; 21(2):56-61. PubMed ID: 4388355
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  • 7. Adams-Oliver syndrome associated with congenital heart defect: not a coincidence.
    David A, Rozé JC, Melon-David V.
    Am J Med Genet; 1991 Jul 01; 40(1):126-7. PubMed ID: 1887843
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  • 8. [Congenital heart defects associated with developmental abnormalities of the fingers].
    Fonó R.
    Orv Hetil; 1966 Jun 12; 107(24):1126-9. PubMed ID: 5944848
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  • 10. Noonan syndrome with bilateral ureteral ectopia.
    Hellebusch AA.
    J Pediatr Surg; 1971 Aug 12; 6(4):490. PubMed ID: 5563894
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  • 14. [Postaxial polydactyly in a female neonate associated with hydrocolpos due to vaginal atresia and with a congenital cardiopathy: the McKusick-Kaufman syndrome].
    Castel Y, Toudic L, Alix D, Le Guern H, Colin A.
    J Genet Hum; 1982 Nov 12; 30(4):329-37. PubMed ID: 7169598
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  • 17. Association of pulmonary hypoplasia, renal anomalies, and Potter's facies.
    Fraga JR, Mirza AM, Reichelderfer TE.
    Clin Pediatr (Phila); 1973 Mar 12; 12(3):150-3. PubMed ID: 4144828
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  • 20. Osteochondritis dissecans with associated malformations in two brothers. A review of familial aspects.
    Hanley WB, McKusick VA, Barranco FT.
    J Bone Joint Surg Am; 1967 Jul 12; 49(5):925-37. PubMed ID: 4382085
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