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Total anonychia congenita in a woman with normal intelligence : Report of a further casePRIOLO, M; ROSAIA, L; SERI, M et al.Dermatology (Basel). 2000, Vol 200, Num 1, pp 84-85, issn 1018-8665Article

Congenital brachydactyly and nail hypoplasia : clue to bone-dependent nail formationSEITZ, C. S; HAMM, H.British journal of dermatology (1951). 2005, Vol 152, Num 6, pp 1339-1342, issn 0007-0963, 4 p.Article

The gene encoding R-spondin 4 (RSPO4), a secreted protein implicated in Wnt signaling, is mutated in inherited anonychiaBLAYDON, Diana C; ISHII, Yoshiyuki; WATSON, Rosemarie et al.Nature genetics. 2006, Vol 38, Num 11, pp 1245-1247, issn 1061-4036, 3 p.Article

Troubles rares de la différenciation : anonychie et ichtyose en maillot de bain = Rare differentiation disorders : anonchia and ichthyosis of the groin areaDEREURE, O.Annales de dermatologie et de vénéréologie. 2007, Vol 134, Num 8-9, issn 0151-9638, 706Article

Anonychie congenitale = The image : Congenital anonychiaMETE, David; HURBIN, Elise; WIND, Patricia et al.La Revue du praticien (Paris). 2006, Vol 56, Num 17, pp 1874-1874, issn 0035-2640, 1 p.Article

Mutations in R-Spondin 4 (RSP04) Underlie Inherited AnonychiaISHII, Yoshiyuki; WAJID, Muhammad; BAZZI, Hisham et al.Journal of investigative dermatology. 2008, Vol 128, Num 4, pp 867-870, issn 0022-202X, 4 p.Article

Mammary-digital-nail (MDN) syndrome: a novel phenotype maps to human chromosome 22q12.3-13.1GENZER-NIR, Mira; KHAYAT, Morad; KOGAN, Leonid et al.European journal of human genetics. 2010, Vol 18, Num 6, pp 662-667, issn 1018-4813, 6 p.Article

The Wnt signalling ligand RSPO4, causing inherited anonychia, is not mutated in a patient with congenital nail hypoplasia/aplasia with underlying skeletal defectsSEITZ, C. S; VAN STEENSEL, M; FRANK, J et al.British journal of dermatology (1951). 2007, Vol 157, Num 4, pp 801-802, issn 0007-0963, 2 p.Article

Herlitz junctional epidermolysis bullosa presenting at birth with anonychia : A case report and review of H-JEBPARSAPOUR, Kourosh; REEP, Michael D; MOHAMMED, Layla et al.Pediatric dermatology. 2001, Vol 18, Num 3, pp 217-222, issn 0736-8046Article

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Fontaine―Farriaux Syndrome: A Recognizable Craniosynostosis Syndrome With Nail, Skeletal, Abdominal, and Central Nervous System AnomaliesCASTORI, Marco; SILVESTRI, Evelina; PEDACE, Lucia et al.American journal of medical genetics. Part A. 2009, Vol 149, Num 10, pp 2193-2199, issn 1552-4825, 7 p.Article

RSP04 Is the Major Gene in Autosomal-Recessive Anonychia and Mutations Cluster in the Furin-Like Cysteine-Rich Domains of the Wnt Signaling Ligand R-spondin 4BRÜCHLE, Nadina Ortiz; FRANK, Jorge; FRANK, Valeska et al.Journal of investigative dermatology. 2008, Vol 128, Num 4, pp 791-796, issn 0022-202X, 6 p.Article

A Previously Undescribed Syndrome Combining Fibular Agenesis/Hypoplasia, Oligodactylous Clubfeet, Anonychia/Ungual Hypoplasia, and Other DefectsSANTOS, Silvana C; PARDONO, Eliete; KOK, Fernando et al.American journal of medical genetics. Part A. 2008, Vol 146, Num 24, pp 3126-3131, issn 1552-4825, 6 p.Article

Mutations in the gene encoding the wnt-signaling component R-spondin 4 (RSPO4) cause autosomal recessive anonychiaBERGMANN, C; SENDEREK, J; NÜRNBERG, P et al.American journal of human genetics. 2006, Vol 79, Num 6, pp 1105-1109, issn 0002-9297, 5 p.Article

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