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Journal Abstract Search

148 related items for PubMed ID: 6702899

  • 1. Familial congenital diaphragmatic defects: aspects of etiology, prenatal diagnosis, and treatment.
    Norio R, Kääriäinen H, Rapola J, Herva R, Kekomäki M.
    Am J Med Genet; 1984 Feb; 17(2):471-83. PubMed ID: 6702899
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  • 2. Autosomal recessive congenital diaphragmatic defects in the Arabs.
    Farag TI, Bastaki L, Marafie M, al-Awadi SA, Krsz J.
    Am J Med Genet; 1994 Apr 15; 50(3):300-1. PubMed ID: 8042677
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  • 3. [Clinical-genealogic analysis of diaphragmatic hernias].
    Il'ina EG.
    Genetika; 1992 Jul 15; 28(7):165-71. PubMed ID: 1427052
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  • 4. Outcomes of congenital diaphragmatic hernia: a population-based study in Western Australia.
    Colvin J, Bower C, Dickinson JE, Sokol J.
    Pediatrics; 2005 Sep 15; 116(3):e356-63. PubMed ID: 16140678
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  • 5. [Congenital defects of the diaphragm in siblings. Two case reports (author's transl)].
    Wolff G, Böhm N, Pringsheim W.
    Monatsschr Kinderheilkd (1902); 1980 Jun 15; 128(6):412-4. PubMed ID: 7421866
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  • 10. Familial diaphragmatic defects: early prenatal diagnosis and evidence for major gene inheritance.
    Bocian M, Spence MA, Marazita ML, Walker AP, Weissberg DL.
    Am J Med Genet Suppl; 1986 Jun 15; 2():163-76. PubMed ID: 3146286
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  • 12. Familial congenital diaphragmatic hernia in the pig--studies on pathology and heredity.
    Ohkawa H, Matsumoto M, Hori T, Kashiwa H.
    Eur J Pediatr Surg; 1993 Apr 15; 3(2):67-71. PubMed ID: 8323920
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  • 13. Familial congenital diaphragmatic hernia: prenatal diagnostic approach and analysis of twelve families.
    Crane JP.
    Clin Genet; 1979 Oct 15; 16(4):244-52. PubMed ID: 519894
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  • 15. [The genetics of familial cases of diaphragmatic hernia].
    Vygovskaia TV, Lur'e IV.
    Tsitol Genet; 1988 Oct 15; 22(2):67-8. PubMed ID: 3413823
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  • 17. Melnick-Needles syndrome: indication for an autosomal recessive form.
    ter Haar B, Hamel B, Hendriks J, de Jager J.
    Am J Med Genet; 1982 Dec 15; 13(4):469-77. PubMed ID: 7158646
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  • 18. [Manifestations and prognosis of congenital diaphragmatic hernia].
    Hentschel R, Wiethoff L, Hülskamp G, Tercanli S, Holzgreve W, Becker C, Jorch G.
    Z Geburtshilfe Perinatol; 1994 Dec 15; 198(3):81-7. PubMed ID: 7941628
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  • 19. The Cohen syndrome: does mottled retina separate a Finnish and a Jewish type?
    Kondo I, Nagataki S, Miyagi N.
    Am J Med Genet; 1990 Sep 15; 37(1):109-13. PubMed ID: 2240027
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  • 20. Genetic aspects in myasthenia gravis. A family study of 264 Finnish patients.
    Pirskanen R.
    Acta Neurol Scand; 1977 Nov 15; 56(5):365-88. PubMed ID: 596124
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