These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

86 related items for PubMed ID: 7093017

  • 21. Lacrimo-auriculo-dento-digital (LADD) syndrome with renal and foot anomalies.
    Roodhooft AM, Brussaard CC, Elst E, van Acker KJ.
    Clin Genet; 1990 Sep; 38(3):228-32. PubMed ID: 2225531
    [Abstract] [Full Text] [Related]

  • 22. Syndrome of tibial hypoplasia with polydactyly-syndactyly in two generations.
    Karamitsos S, Bartsocas CS.
    Prog Clin Biol Res; 1982 Sep; 104():289-97. PubMed ID: 6298813
    [No Abstract] [Full Text] [Related]

  • 23. [Cowden's syndrome (multiple hamartoma syndrome)].
    Toonstra J, van Heijst PJ.
    Ned Tijdschr Geneeskd; 1984 Jul 14; 128(28):1328-30. PubMed ID: 6482990
    [No Abstract] [Full Text] [Related]

  • 24.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 25. Liver cysts in patients with autosomal dominant polysystic kidney disease.
    Gandhi RM, Patil RA, Mehta NP, Thomas C.
    J Assoc Physicians India; 1993 Nov 14; 41(11):723. PubMed ID: 8005928
    [No Abstract] [Full Text] [Related]

  • 26. [Autosomal dominant transmission in retinitis pigmentosa].
    Ghenoiu R.
    Oftalmologia; 1993 Nov 14; 37(4):339-41. PubMed ID: 8286320
    [Abstract] [Full Text] [Related]

  • 27.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 28.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 29. ADULT-syndrome: an autosomal-dominant disorder with pigment anomalies, ectrodactyly, nail dysplasia, and hypodontia.
    Propping P, Zerres K.
    Am J Med Genet; 1993 Mar 01; 45(5):642-8. PubMed ID: 8456838
    [Abstract] [Full Text] [Related]

  • 30. Asphyxiating thoracic dystrophy and syndactyly of the toes in a newborn: coincidence or a new association?
    Tastekin A, Polat P, Ors R.
    Genet Couns; 2003 Mar 01; 14(1):113-4. PubMed ID: 12725597
    [No Abstract] [Full Text] [Related]

  • 31. Congenital diaphragmatic defects and associated syndromes, malformations, and chromosome anomalies: a retrospective study of 60 patients and literature review.
    Enns GM, Cox VA, Goldstein RB, Gibbs DL, Harrison MR, Golabi M.
    Am J Med Genet; 1998 Sep 23; 79(3):215-25. PubMed ID: 9788565
    [Abstract] [Full Text] [Related]

  • 32. Cerebro-costo-mandibular syndrome with autosomal dominant inheritance.
    Leroy JG, Devos EA, Vanden Bulcke LJ, Robbe NS.
    J Pediatr; 1981 Sep 23; 99(3):441-3. PubMed ID: 7264806
    [No Abstract] [Full Text] [Related]

  • 33. Is the autosomal dominant Optiz GBBB syndrome part of the DiGeorge/velocardiofacial syndrome with deletions of chromosome area 22q11.2?
    Wulfsberg EA.
    Am J Med Genet; 1996 Aug 23; 64(3):523-4. PubMed ID: 8862634
    [No Abstract] [Full Text] [Related]

  • 34. Syndactyly of the ring and small finger.
    De Smet L, Mulier T, Fabry G.
    Genet Couns; 1994 Aug 23; 5(1):45-9. PubMed ID: 8031535
    [Abstract] [Full Text] [Related]

  • 35.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 36.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 37. Developmental pathogenesis of chromosome disorders: a final word.
    Langenbeck U.
    Am J Med Genet; 1988 Oct 23; 31(2):479-80. PubMed ID: 3232711
    [No Abstract] [Full Text] [Related]

  • 38. [Isolated symbrachydactyly of the foot].
    Falliner A.
    Z Orthop Ihre Grenzgeb; 1988 Oct 23; 126(2):125-6. PubMed ID: 3407296
    [Abstract] [Full Text] [Related]

  • 39.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 40.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 5.