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PubMed (cited) for id: 300707
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STAR syndrome: a further case and the first report of maternal mosaicism.
Clin Dysmorphol. 2017 Jul;26(3):157-160. doi: 10.1097/MCD.0000000000000176.
Clin Dysmorphol. 2017.
PMID: 28225384
Review.
No abstract available.
Mutations in the cyclin family member FAM58A cause an X-linked dominant disorder characterized by syndactyly, telecanthus and anogenital and renal malformations.
Unger S, Böhm D, Kaiser FJ, Kaulfuss S, Borozdin W, Buiting K, Burfeind P, Böhm J, Barrionuevo F, Craig A, Borowski K, Keppler-Noreuil K, Schmitt-Mechelke T, Steiner B, Bartholdi D, Lemke J, Mortier G, Sandford R, Zabel B, Superti-Furga A, Kohlhase J.
Unger S, et al.
Nat Genet. 2008 Mar;40(3):287-9. doi: 10.1038/ng.86. Epub 2008 Feb 24.
Nat Genet. 2008.
PMID: 18297069
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An autosomal dominant syndrome of renal and anogenital malformations with syndactyly.
Green AJ, Sandford RN, Davison BC.
Green AJ, et al.
J Med Genet. 1996 Jul;33(7):594-6. doi: 10.1136/jmg.33.7.594.
J Med Genet. 1996.
PMID: 8818947
Free PMC article.
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