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Journal Abstract Search

115 related items for PubMed ID: 4702713

  • 21. Total anonychia congenita: a rare heterogeneic disorder.
    Ozdemir O, Tiftikcioglu YO, Karaaslan O, Ozdemir R, Kocer U.
    Genet Couns; 2004; 15(1):43-6. PubMed ID: 15083698
    [Abstract] [Full Text] [Related]

  • 22. Hereditary sensorineural hearing loss associated with onychodystrophy and digital malformations.
    Moghadam H, Statten P.
    Can Med Assoc J; 1972 Aug 19; 107(4):310-2. PubMed ID: 5056117
    [No Abstract] [Full Text] [Related]

  • 23. Odontoonychodermal dysplasia: a previously apparently undescribed ectodermal dysplasia.
    Fadhil M, Ghabra TA, Deeb M, Der Kaloustian VM.
    Am J Med Genet; 1983 Feb 19; 14(2):335-46. PubMed ID: 6837628
    [Abstract] [Full Text] [Related]

  • 24. The Meckel syndrome in Finland: epidemiologic and genetic aspects.
    Salonen R, Norio R.
    Am J Med Genet; 1984 Aug 19; 18(4):691-8. PubMed ID: 6486168
    [Abstract] [Full Text] [Related]

  • 25. Anonychia with ectrodactyly: a South Indian predigree study.
    Yesudian P, Subramaniam P, Thambiah AS.
    Int J Dermatol; 1977 Sep 19; 16(7):599-604. PubMed ID: 914414
    [No Abstract] [Full Text] [Related]

  • 26. [Jadassohn-Lewandowski syndrome with polydactylia and alopecia of the eyebrows].
    FONTAINE A, WELLENS W.
    Arch Belg Dermatol Syphiligr; 1958 Jun 19; 14(2):178-84. PubMed ID: 13559994
    [No Abstract] [Full Text] [Related]

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

  • 28. Autosomal dominant onychodystrophy and anonychia with type B brachydactyly and ectrodactyly.
    Kumar D, Levick RK.
    Clin Genet; 1986 Sep 19; 30(3):219-25. PubMed ID: 3780038
    [Abstract] [Full Text] [Related]

  • 29. Trigonocephaly and associated minor anomalies in mother and son.
    Hunter AG, Rudd NL, Hoffmann HJ.
    J Med Genet; 1976 Feb 19; 13(1):77-9. PubMed ID: 1271432
    [Abstract] [Full Text] [Related]

  • 30. [Coffin-Siris syndrome. Critical study of the literature apropos of a case].
    Foasso MF, Hermier M, Descos B, Collet JP, Perron F.
    Pediatrie; 1983 Mar 19; 38(2):111-7. PubMed ID: 6622139
    [Abstract] [Full Text] [Related]

  • 31. Corneal changes, hyperkeratosis, short stature, brachydactyly, and premature birth: a new autosomal dominant syndrome.
    Stern JK, Lubinsky MS, Durrie DS, Luckasen JR.
    Am J Med Genet; 1984 May 19; 18(1):67-77. PubMed ID: 6234802
    [Abstract] [Full Text] [Related]

  • 32. [Nanism and onychodysplasia (on a case of Senior's syndrome)].
    Lugli T.
    Chir Organi Mov; 1975 May 19; 62(2):175-80. PubMed ID: 1222594
    [No Abstract] [Full Text] [Related]

  • 33. Anonychia of all toes with absence of phalangeal bones.
    Hatzis J, Soulacos PN.
    Australas J Dermatol; 1994 May 19; 35(2):83-6. PubMed ID: 7702494
    [Abstract] [Full Text] [Related]

  • 34. Recessively inherited brachydactyly type C.
    Baraitser M, Burn J.
    J Med Genet; 1983 Apr 19; 20(2):128-9. PubMed ID: 6842546
    [Abstract] [Full Text] [Related]

  • 35. Total congenital anonychia.
    Afsar FS, Karakuzu A.
    Pediatr Dermatol; 2014 Apr 19; 31(6):743-4. PubMed ID: 25424215
    [Abstract] [Full Text] [Related]

  • 36. Brachydactyly type B and symphalangism in different members of a Mexican family.
    Zavala C, Hernández-Ortíz J, Lisker R.
    Ann Genet; 1975 Jun 19; 18(2):131-4. PubMed ID: 1081366
    [Abstract] [Full Text] [Related]

  • 37. Anonychia with ectrodactyly: clinical and linkage data.
    LEES DH, LAWLER SD, RENWICK JH, THODAY JM.
    Ann Hum Genet; 1957 Oct 19; 22(1):69-79. PubMed ID: 13488188
    [No Abstract] [Full Text] [Related]

  • 38. [Developmental abnormalities of the finger- and toenails].
    Weyers H.
    Dtsch Krankenpflegez; 1971 Dec 19; 24(12):603-7. PubMed ID: 5210394
    [No Abstract] [Full Text] [Related]

  • 39. Mutation in the HPGD gene encoding NAD+ dependent 15-hydroxyprostaglandin dehydrogenase underlies isolated congenital nail clubbing (ICNC).
    Tariq M, Azeem Z, Ali G, Chishti MS, Ahmad W.
    J Med Genet; 2009 Jan 19; 46(1):14-20. PubMed ID: 18805827
    [Abstract] [Full Text] [Related]

  • 40. Anonychia Congenita - Rare Inheritance of a Rare Disorder.
    Vasudha J, Jalees F, S P, Raj VA, Tauseef KM.
    J Assoc Physicians India; 2022 Dec 19; 69(12):11-12. PubMed ID: 35057601
    [Abstract] [Full Text] [Related]

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