## Communicated by Iain McIntosh Feingold syndrome (FS) is the most frequent cause of familial syndromic gastrointestinal atresia and follows autosomal dominant inheritance. FS is caused by germline mutations in or deletions of the MYCN gene. Previously, 12 different heterozygous MYCN mutations and
Genotype–phenotype correlations forSLC26A4-related deafness
✍ Scribed by Hela Azaiez; Tao Yang; Sai Prasad; Jessica L. Sorensen; Carla J. Nishimura; William J. Kimberling; Richard J. H. Smith
- Publisher
- Springer
- Year
- 2007
- Tongue
- English
- Weight
- 468 KB
- Volume
- 122
- Category
- Article
- ISSN
- 0340-6717
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