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Items: 7

1.

Zeb2: A multifunctional regulator of nervous system development.

Hegarty SV, Sullivan AM, O'Keeffe GW.

Prog Neurobiol. 2015 Sep;132:81-95. doi: 10.1016/j.pneurobio.2015.07.001. Epub 2015 Jul 18. Review.

PMID:
26193487
2.

Hirschsprung's disease in children with Mowat-Wilson syndrome.

Coyle D, Puri P.

Pediatr Surg Int. 2015 Aug;31(8):711-7. doi: 10.1007/s00383-015-3732-x. Epub 2015 Jul 9. Review.

PMID:
26156877
3.

If not Angelman, what is it? A review of Angelman-like syndromes.

Tan WH, Bird LM, Thibert RL, Williams CA.

Am J Med Genet A. 2014 Apr;164A(4):975-92. Review.

PMID:
24779060
4.

Mowat-Wilson syndrome: facial phenotype changing with age: study of 19 Italian patients and review of the literature.

Garavelli L, Zollino M, Mainardi PC, Gurrieri F, Rivieri F, Soli F, Verri R, Albertini E, Favaron E, Zignani M, Orteschi D, Bianchi P, Faravelli F, Forzano F, Seri M, Wischmeijer A, Turchetti D, Pompilii E, Gnoli M, Cocchi G, Mazzanti L, Bergamaschi R, De Brasi D, Sperandeo MP, Mari F, Uliana V, Mostardini R, Cecconi M, Grasso M, Sassi S, Sebastio G, Renieri A, Silengo M, Bernasconi S, Wakamatsu N, Neri G.

Am J Med Genet A. 2009 Mar;149A(3):417-26. doi: 10.1002/ajmg.a.32693. Review.

PMID:
19215041
5.

Mowat-Wilson syndrome.

Garavelli L, Mainardi PC.

Orphanet J Rare Dis. 2007 Oct 24;2:42. Review.

6.

Atypical ZFHX1B mutation associated with a mild Mowat-Wilson syndrome phenotype.

Zweier C, Horn D, Kraus C, Rauch A.

Am J Med Genet A. 2006 Apr 15;140(8):869-72. Review.

PMID:
16532472
7.

Mowat-Wilson syndrome.

Mowat DR, Wilson MJ, Goossens M.

J Med Genet. 2003 May;40(5):305-10. Review.

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