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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

159 related items for PubMed ID: 37158316

  • 21.
    ; . PubMed ID:
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  • 22. TP63 gene mutations in Chinese P63 syndrome patients.
    Yin W, Ye X, Shi L, Wang QK, Jin H, Wang P, Bian Z.
    J Dent Res; 2010 Aug; 89(8):813-7. PubMed ID: 20410354
    [Abstract] [Full Text] [Related]

  • 23. Familial cleft tongue caused by a unique translation initiation codon variant in TP63.
    Schmidt J, Schreiber G, Altmüller J, Thiele H, Nürnberg P, Li Y, Kaulfuß S, Funke R, Wilken B, Yigit G, Wollnik B.
    Eur J Hum Genet; 2022 Feb; 30(2):211-218. PubMed ID: 34629465
    [Abstract] [Full Text] [Related]

  • 24.
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  • 25. Novel phenotype of syndromic premature ovarian insufficiency associated with TP63 molecular defect.
    Mathorne SW, Ravn P, Hansen D, Beck-Nielsen SS, Gjørup H, Sørensen KP, Fagerberg CR.
    Clin Genet; 2020 May; 97(5):779-784. PubMed ID: 32067224
    [Abstract] [Full Text] [Related]

  • 26. Recurrence of split hand/foot malformation, cleft lip/palate, and severe urogenital abnormalities due to germline mosaicism for TP63 mutation.
    Enriquez A, Krivanek M, Flöttmann R, Peters H, Wilson M.
    Am J Med Genet A; 2016 Sep; 170(9):2372-6. PubMed ID: 27351625
    [Abstract] [Full Text] [Related]

  • 27. Absent meibomian glands in the ectrodactyly, ectodermal dysplasia, cleft lip-palate syndrome.
    Mondino BJ, Bath PE, Foos RY, Apt L, Rajacich GM.
    Am J Ophthalmol; 1984 Apr; 97(4):496-500. PubMed ID: 6720821
    [Abstract] [Full Text] [Related]

  • 28. Limbal stem cell deficiency and ocular phenotype in ectrodactyly-ectodermal dysplasia-clefting syndrome caused by p63 mutations.
    Di Iorio E, Kaye SB, Ponzin D, Barbaro V, Ferrari S, Böhm E, Nardiello P, Castaldo G, McGrath JA, Willoughby CE.
    Ophthalmology; 2012 Jan; 119(1):74-83. PubMed ID: 21959367
    [Abstract] [Full Text] [Related]

  • 29. Infrared meibography and molecular assessment of p63 gene mutations in a Mexican patient with EEC syndrome.
    Garza-Leon M, León-Cachón RBR, Villafuerte-de la Cruz R, Martínez-Treviño DA.
    Arch Soc Esp Oftalmol (Engl Ed); 2018 Nov; 93(11):562-566. PubMed ID: 30025988
    [Abstract] [Full Text] [Related]

  • 30. Novel variant in the TP63 gene associated to ankyloblepharon-ectodermal dysplasia-cleft lip/palate (AEC) syndrome.
    Gonzalez F, Loidi L, Abalo-Lojo JM.
    Ophthalmic Genet; 2017 Nov; 38(3):277-280. PubMed ID: 27485918
    [Abstract] [Full Text] [Related]

  • 31. A novel H208D TP63 mutation in a familial case of ectrodactyly-ectodermal dysplasia-cleft lip/palate syndrome without clefting.
    Sorasio L, Biamino E, Garelli E, Ferrero GB, Silengo MC.
    Clin Exp Dermatol; 2009 Dec; 34(8):e726-8. PubMed ID: 19663851
    [Abstract] [Full Text] [Related]

  • 32. Tooth defects of EEC and AEC syndrome caused by heterozygous TP63 mutations in three Chinese families and genotype-phenotype correlation analyses of TP63-related disorders.
    Zheng J, Liu H, Zhan Y, Liu Y, Wong SW, Cai T, Feng H, Han D.
    Mol Genet Genomic Med; 2019 Jun; 7(6):e704. PubMed ID: 31050217
    [Abstract] [Full Text] [Related]

  • 33. A case of ankyloblepharon, ectodermal dysplasia, and cleft lip/palate syndrome with ectrodactyly: are the p63 syndromes distinct after all?
    Chiu YE, Drolet BA, Duffy KJ, Holland KE.
    Pediatr Dermatol; 2011 Jun; 28(1):15-9. PubMed ID: 19793345
    [Abstract] [Full Text] [Related]

  • 34. Ectrodactyly, ectodermal dysplasia, and cleft lip-palate (EEC) syndrome without clefting: a rare case report.
    Malvankar DD, Sacchidanand S, Mallikarjun M.
    Dermatol Online J; 2012 Feb 15; 18(2):5. PubMed ID: 22398226
    [Abstract] [Full Text] [Related]

  • 35. [Ectrodactyly-ectodermal dysplasia-clefting (EEC) syndrome].
    Bartalis K, Kálmán B, Kisely M.
    Orv Hetil; 2023 Nov 19; 164(46):1831-1837. PubMed ID: 37980600
    [Abstract] [Full Text] [Related]

  • 36. Personalized Stem Cell Therapy to Correct Corneal Defects Due to a Unique Homozygous-Heterozygous Mosaicism of Ectrodactyly-Ectodermal Dysplasia-Clefting Syndrome.
    Barbaro V, Nasti AA, Raffa P, Migliorati A, Nespeca P, Ferrari S, Palumbo E, Bertolin M, Breda C, Miceli F, Russo A, Caenazzo L, Ponzin D, Palù G, Parolin C, Di Iorio E.
    Stem Cells Transl Med; 2016 Aug 19; 5(8):1098-105. PubMed ID: 27151912
    [Abstract] [Full Text] [Related]

  • 37. Sweating ability of patients with p63-associated syndromes.
    Ferstl P, Wohlfart S, Schneider H.
    Eur J Pediatr; 2018 Nov 19; 177(11):1727-1731. PubMed ID: 30088137
    [Abstract] [Full Text] [Related]

  • 38. ADULT syndrome: phenotype in a Brazilian family with the R298Q mutation.
    de Almeida HL, van Steensel M, Rocha A, Caspary P, Meijer R.
    Int J Dermatol; 2019 Mar 19; 58(3):e72-e75. PubMed ID: 30656674
    [No Abstract] [Full Text] [Related]

  • 39. 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]

  • 40. 'Double trouble': diagnostic challenges in genetic skin disorders.
    Kiritsi D, Valari M, Mileounis K, Bruckner-Tuderman L, Has C.
    Br J Dermatol; 2015 Jan 01; 172(1):276-8. PubMed ID: 24902867
    [No Abstract] [Full Text] [Related]

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