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Pubmed for Handhelds

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Journal Abstract Search

435 related items for PubMed ID: 7158646

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  • 5. Mandibulofacial dysostosis in Hutterite sibs: a possible recessive trait.
    Lowry RB, Morgan K, Holmes TM, Metcalf PJ, Stauffer GF.
    Am J Med Genet; 1985 Nov; 22(3):501-12. PubMed ID: 4061487
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  • 7. [Hydrometrocolpos, polydactylia and congenital heart defect (the McKusick-Dungy-Kaufman syndrome)].
    Hamel BC, ter Haar BG.
    Tijdschr Kindergeneeskd; 1984 Aug; 52(4):129-33. PubMed ID: 6495304
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  • 13. A syndrome of severe midface retraction, multiple skull anomalies, clubfeet, and cardiac and renal malformations in sibs.
    Schinzel A, Giedion A.
    Am J Med Genet; 1978 Aug; 1(4):361-75. PubMed ID: 665725
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  • 14. Anterior segment anomalies of the eye associated with multiple skeletal abnormalities and early lethality: confirmation of an autosomal recessive syndrome.
    al-Gazali LI, Bakir M, Sadaghatian MR, Nath R, Haas D.
    Clin Dysmorphol; 1999 Apr; 8(2):87-92. PubMed ID: 10319196
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  • 15. Melnick-Needles syndrome in males: a lethal multiple congenital anomalies syndrome.
    Donnenfeld AE, Conard KA, Roberts NS, Borns PF, Zackai EH.
    Am J Med Genet; 1987 May; 27(1):159-73. PubMed ID: 3605194
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  • 16. [A genetic study and clinical classification of 154 cases of mandibulofacial dystosis (Franceschetti's syndrome), with descriptions of associated malformations].
    Vatré JL.
    J Genet Hum; 1971 Mar; 19(1):17-100. PubMed ID: 5003458
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  • 17. Lethal faciocardiomelic dysplasia- a new autosomal recessive disorder.
    Cantú JM, Hernández A, Ramírez J, Bernal M, Rubio G, Urrusti J, Franco-Vázquez S.
    Birth Defects Orig Artic Ser; 1975 Mar; 11(5):91-8. PubMed ID: 1218241
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  • 19. Autosomal recessive syndrome of sacral and conotruncal developmental field defects (Kousseff syndrome).
    Toriello HV, Sharda JK, Beaumont EJ.
    Am J Med Genet; 1985 Oct; 22(2):357-60. PubMed ID: 4050868
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  • 20. Mandibulofacial dysostosis: report on two Brazilian families suggesting autosomal recessive inheritance.
    Richieri-Costa A, Bortolozo MA, Lauris JR, Lauris RC, Guion-Almeida ML, Marques D, Moreti D.
    Am J Med Genet; 1993 Jul 01; 46(6):659-64. PubMed ID: 8362908
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