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PUBMED FOR HANDHELDS

Journal Abstract Search


165 related items for PubMed ID: 457141

  • 21. Oto-palato-digital syndrome.
    Gorlin RJ.
    Am J Dis Child; 1967 Aug; 114(2):215. PubMed ID: 4951552
    [No Abstract] [Full Text] [Related]

  • 22. A study of the family histories of patients with hare lip and cleft palate.
    Stonova NS, Messina VM.
    Sov Genet; 1974 Jul 01; 8(6):777-82. PubMed ID: 4425041
    [No Abstract] [Full Text] [Related]

  • 23. X-linked Dyggve-Melchior-Clausen syndrome.
    Yunis E, Fontalvo J, Quintero L.
    Clin Genet; 1980 Oct 01; 18(4):284-90. PubMed ID: 7192195
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  • 24. Autosomal dominant Klippel-Feil anomaly with cleft palate.
    Thompson E, Haan E, Sheffield L.
    Clin Dysmorphol; 1998 Jan 01; 7(1):11-5. PubMed ID: 9546824
    [Abstract] [Full Text] [Related]

  • 25. Linkage analysis of X-linked cleft palate and ankyloglossia in Manitoba Mennonite and British Columbia Native kindreds.
    Gorski SM, Adams KJ, Birch PH, Chodirker BN, Greenberg CR, Goodfellow PJ.
    Hum Genet; 1994 Aug 01; 94(2):141-8. PubMed ID: 8045560
    [Abstract] [Full Text] [Related]

  • 26. Sex-linked cleft palate in a British Columbia Indian family.
    Lowry RB.
    Pediatrics; 1970 Jul 01; 46(1):123-8. PubMed ID: 5423440
    [No Abstract] [Full Text] [Related]

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  • 29. Transgenic mouse model of X-linked cleft palate.
    Wilson JB, Ferguson MW, Jenkins NA, Lock LF, Copeland NG, Levine AJ.
    Cell Growth Differ; 1993 Feb 01; 4(2):67-76. PubMed ID: 8494785
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  • 30. Three distinct types of X-linked arthrogryposis seen in 6 families.
    Hall JG, Reed SD, Scott CI, Rogers JG, Jones KL, Camarano A.
    Clin Genet; 1982 Feb 01; 21(2):81-97. PubMed ID: 7200838
    [Abstract] [Full Text] [Related]

  • 31. Familial congenital diaphragmatic defect and associated midline anomalies: further evidence for an X-linked midline gene?
    Carmi R, Meizner I, Katz M.
    Am J Med Genet; 1990 Jul 01; 36(3):313-5. PubMed ID: 2363430
    [Abstract] [Full Text] [Related]

  • 32. Dominant inheritance of cleft palate, microstomia and micrognathia--possible linkage to the fragile site at 16q22 (FRA16B).
    McKenzie F, Turner A, Withers S, Dalzell P, McGlynn M, Kirk EP.
    Clin Dysmorphol; 2002 Oct 01; 11(4):237-41. PubMed ID: 12401987
    [Abstract] [Full Text] [Related]

  • 33. An X-linked recessive mutation producing cleft palate, crooked tail, and polydactyly in mice.
    Barra J.
    J Hered; 1990 Oct 01; 81(5):388-92. PubMed ID: 2230077
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  • 35. Congenital contractures, ectodermal dysplasia, cleft lip/palate, and developmental impairment: a distinct syndrome.
    Ladda RL, Zonana J, Ramer JC, Mascari MJ, Rogan PK.
    Am J Med Genet; 1993 Sep 15; 47(4):550-5. PubMed ID: 7504881
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  • 40. Brief clinical report: not all cystic hygromas occur in the Ullrich-Turner syndrome.
    Cowchock FS, Wapner RJ, Kurtz A, Chatzkel S, Barnhart JS, Lesnick DC.
    Am J Med Genet; 1982 Jul 15; 12(3):327-31. PubMed ID: 7114094
    [Abstract] [Full Text] [Related]


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