Mutations in different components of FGF signaling in LADD syndrome

Yerel katalogda bu makaleye atıf yapan 13 yayın (OpenAlex referans eşleşmesi; tam dünya listesi değildir).

1. 2010 A Specific Mutation in the Distant Sonic Hedgehog SHH Cis Regulator ZRS Causes Werner Mesomelic Syndrome WMS While Complete ZRS Duplications Underlie Haas Type Polysyndactyly and Preaxial Polydactyly PPD With or Without Triphalangeal ThumbAtıf 131 · OpenAlex
2. 2007 Homozygous Mutations in Fibroblast Growth Factor 3 Are Associated with a New Form of Syndromic Deafness Characterized by Inner Ear Agenesis, Microtia, and MicrodontiaAtıf 113 · OpenAlex
3. 2007 Homozygous mutations in fibroblast growth factor 3 are associated with a new form of syndromic deafness characterized by inner ear agenesis, microtia, and microdontiaAtıf 113 · OpenAlex
4. 2007 Homozygous Mutations in Fibroblast Growth Factor 3 Are Associated with a New Form of Syndromic Deafness Characterized by Inner Ear Agenesis Microtia and MicrodontiaAtıf 113 · OpenAlex
5. 2007 Homozygous Mutations in Fibroblast Growth Factor 3 Are Associated with a New Form of Syndromic Deafness Characterized by Inner Ear Agenesis Microtia and MicrodontiaAtıf 113 · OpenAlex
6. 2012 Mutations in IRX5 impair craniofacial development and germ cell migration via SDF1Atıf 86 · OpenAlex
7. 2012 Mutations in IRX5 impair craniofacial development and germ cell migration via SDF1Atıf 86 · OpenAlex
8. 2012 Mutations in IRX5 impair craniofacial development and germ cell migration via SDF1Atıf 85 · OpenAlex
9. 2016 Novel FGF10 mutation in autosomal dominant aplasia of lacrimal and salivary glandsAtıf 21 · OpenAlex
10. 2016 Novel FGF10 mutation in autosomal dominant aplasia of lacrimal and salivary glandsAtıf 21 · OpenAlex