PubMed (cited) for id: 103285

Year	Number of Results
1993	1
2000	1
2001	2
2002	1
2005	1
2006	2
2008	1
2009	1
2010	1
2024	0

1

Adermatoglyphia, previously unrecognized manifestation in ADULT syndrome.

de Almeida HL Jr, Caspary P, Duquia RP, Meijer R, van Steensel M. de Almeida HL Jr, et al. Am J Med Genet A. 2010 Oct;152A(10):2656-7. doi: 10.1002/ajmg.a.33625. Am J Med Genet A. 2010. PMID: 20814947 No abstract available.

2

A novel TP63 mutation in family with ADULT syndrome presenting with eczema and hypothelia.

van Zelst-Stams WA, van Steensel MA. van Zelst-Stams WA, et al. Am J Med Genet A. 2009 Jul;149A(7):1558-60. doi: 10.1002/ajmg.a.32881. Am J Med Genet A. 2009. PMID: 19530185 No abstract available.

3

R298Q mutation of p63 gene in autosomal dominant ectodermal dysplasia associated with arrhythmogenic right ventricular cardiomyopathy.

Valenzise M, Arrigo T, De Luca F, Privitera A, Frigiola A, Carando A, Garelli E, Silengo M. Valenzise M, et al. Eur J Med Genet. 2008 Sep-Oct;51(5):497-500. doi: 10.1016/j.ejmg.2008.05.005. Epub 2008 May 28. Eur J Med Genet. 2008. PMID: 18603493

4

Further phenotypic and genetic variation in ADULT syndrome.

Reisler TT, Patton MA, Meagher PP. Reisler TT, et al. Am J Med Genet A. 2006 Nov 15;140(22):2495-500. doi: 10.1002/ajmg.a.31482. Am J Med Genet A. 2006. PMID: 17041931

5

Delineation of the ADULT syndrome phenotype due to arginine 298 mutations of the p63 gene.

Rinne T, Spadoni E, Kjaer KW, Danesino C, Larizza D, Kock M, Huoponen K, Savontaus ML, Aaltonen M, Duijf P, Brunner HG, Penttinen M, van Bokhoven H. Rinne T, et al. Eur J Hum Genet. 2006 Aug;14(8):904-10. doi: 10.1038/sj.ejhg.5201640. Epub 2006 May 17. Eur J Hum Genet. 2006. PMID: 16724007

6

Acro-dermato-ungual-lacrimal-tooth (ADULT) syndrome: report of a child with phenotypic overlap with ulnar-mammary syndrome and a new mutation in TP63.

Slavotinek AM, Tanaka J, Winder A, Vargervik K, Haggstrom A, Bamshad M. Slavotinek AM, et al. Am J Med Genet A. 2005 Oct 1;138A(2):146-9. doi: 10.1002/ajmg.a.30900. Am J Med Genet A. 2005. PMID: 16114047

7

Gain-of-function mutation in ADULT syndrome reveals the presence of a second transactivation domain in p63.

Duijf PH, Vanmolkot KR, Propping P, Friedl W, Krieger E, McKeon F, Dötsch V, Brunner HG, van Bokhoven H. Duijf PH, et al. Hum Mol Genet. 2002 Apr 1;11(7):799-804. doi: 10.1093/hmg/11.7.799. Hum Mol Genet. 2002. PMID: 11929852

8

TP63 gene mutation in ADULT syndrome.

Amiel J, Bougeard G, Francannet C, Raclin V, Munnich A, Lyonnet S, Frebourg T. Amiel J, et al. Eur J Hum Genet. 2001 Aug;9(8):642-5. doi: 10.1038/sj.ejhg.5200676. Eur J Hum Genet. 2001. PMID: 11528512

9

p63 Gene mutations in eec syndrome, limb-mammary syndrome, and isolated split hand-split foot malformation suggest a genotype-phenotype correlation.

van Bokhoven H, Hamel BC, Bamshad M, Sangiorgi E, Gurrieri F, Duijf PH, Vanmolkot KR, van Beusekom E, van Beersum SE, Celli J, Merkx GF, Tenconi R, Fryns JP, Verloes A, Newbury-Ecob RA, Raas-Rotschild A, Majewski F, Beemer FA, Janecke A, Chitayat D, Crisponi G, Kayserili H, Yates JR, Neri G, Brunner HG. van Bokhoven H, et al. Am J Hum Genet. 2001 Sep;69(3):481-92. doi: 10.1086/323123. Epub 2001 Jul 17. Am J Hum Genet. 2001. PMID: 11462173 Free PMC article.

10

ADULT syndrome allelic to limb mammary syndrome (LMS)?

Propping P, Friedl W, Wienker TF, Uhlhaas S, Zerres K. Propping P, et al. Am J Med Genet. 2000 Jan 17;90(2):179-82. Am J Med Genet. 2000. PMID: 10607963

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