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Journal Abstract Search

365 related items for PubMed ID: 47396

  • 21.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 22. Multiple malformation syndrome including cleft lip and palate and cardiac abnormalities due to an interstitial deletion of chromosome 12q.
    Meinecke P, Meinecke R.
    J Med Genet; 1987 Mar; 24(3):187. PubMed ID: 3573007
    [No Abstract] [Full Text] [Related]

  • 23. [A case of Patau syndrome. Fetal heart defect and lip-jaw-palate cleft as indicators].
    Küffer E, Asseryanis E, Eppel W, Schurz B, Reinold E.
    Ultraschall Med; 1994 Aug; 15(4):217-8. PubMed ID: 7973594
    [Abstract] [Full Text] [Related]

  • 24. Terminal tandem duplication of 16p: a case with "pure" partial trisomy (16)(pter-->p13).
    Tschernigg M, Petek E, Leonhardtsberger A, Wagner K, Kroisel PM.
    Genet Couns; 2002 Aug; 13(3):303-7. PubMed ID: 12416638
    [Abstract] [Full Text] [Related]

  • 25. Partial deletion of long arm of chromosome 11[del(11)(q23)]: Jacobsen syndrome. Two new cases and review of the clinical findings.
    Schinzel A, Auf der Maur P, Moser H.
    J Med Genet; 1977 Dec; 14(6):438-44. PubMed ID: 604495
    [Abstract] [Full Text] [Related]

  • 26.
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  • 27. A, 1;6, translocation associated with congenital glaucoma and cleft lip and palate.
    Tinning S, Jacobsen P, Mikkelsen M.
    Hum Hered; 1975 Dec; 25(6):453-60. PubMed ID: 1225819
    [Abstract] [Full Text] [Related]

  • 28. Trisomy 22. Two new cases and delineation of the phenotype.
    Penchaszadeh VB, Coco R.
    J Med Genet; 1975 Jun; 12(2):193-9. PubMed ID: 49427
    [Abstract] [Full Text] [Related]

  • 29.
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  • 30.
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  • 31. An autosomal dominant midline cleft syndrome resembling familial holoprosencephaly.
    Martin AO, Perrin JC, Muir WA, Ruch E, Schafer IA.
    Clin Genet; 1977 Aug; 12(2):65-72. PubMed ID: 891015
    [Abstract] [Full Text] [Related]

  • 32. [CHROMOSOME ABNORMALITIES AND HUMAN DISEASES. CONTRIBUTION TO THE ANATOMICAL STUDY OF TRISOMY 13].
    LAFOURCADE J, BOCQUET L, CRUVEILLER J, SARAUX H, BERGER R, LEJEUNE J, HUETDEBAROCHEZ Y, TURPIN R.
    Bull Mem Soc Med Hop Paris; 1977 Aug; 115():383-99. PubMed ID: 14156094
    [No Abstract] [Full Text] [Related]

  • 33.
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  • 34.
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  • 35. Arrhinencephaly associated with a deficiency involving chromosome 18.
    McDermott A, Insley J, Barton ME, Roowe P, Edwards JH, Cameron AH.
    J Med Genet; 1968 Mar; 5(1):60-7. PubMed ID: 5653872
    [No Abstract] [Full Text] [Related]

  • 36. Monosomy and trisomy of 15q24-qter with cleft lip and palate.
    Abe A, Hatano Y, Kurita K, Nakano M, Shimizu M, Yokoi T, Sugiyama N.
    Int J Oral Maxillofac Surg; 2008 May; 37(5):487-90. PubMed ID: 18262763
    [Abstract] [Full Text] [Related]

  • 37. Proximal deletion of the long arm of chromosome 1: [del(1)(q23-q25)].
    Lo LJ, Noordhoff MS, Huang CS, Chen KT, Chen YR.
    Cleft Palate Craniofac J; 1993 Nov; 30(6):586-9. PubMed ID: 8280739
    [Abstract] [Full Text] [Related]

  • 38.
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  • 39. Familial partial trisomy of the long arm of chromosome 10 (q24-26).
    Moreno-Fuenmayor H, Zackai EH, Mellman WJ, Aronson M.
    Pediatrics; 1975 Nov; 56(5):756-61. PubMed ID: 1196732
    [Abstract] [Full Text] [Related]

  • 40.
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