Can I read Craniosynostosis suggestive of Saethre-Chotzen syndrome: Clinical description of a large kindred and exclusion of candidate regions on 7p on EtoBox?
Craniosynostosis suggestive of Saethre-Chotzen syndrome: Clinical description of a large kindred and exclusion of candidate regions on 7p by von Gernet, Steven; Schuffenhauer, Simone; Golla, Astrid; Lichtner, Peter; Balg, Stefanie; Mühlbauer, Wolfgang; Murken, Jan; Fairley, Jeffrey; Meitinger, Thomas is a Biochemistry, Genetics and Molecular Biology article available to read on EtoBox.
What is Craniosynostosis suggestive of Saethre-Chotzen syndrome: Clinical description of a large kindred and exclusion of candidate regions on 7p about?
W e decribe the clinical manifestations of an autosomal dominant form of craniosynostosis in a large family with eight affected relatives. Unilateral or bilateral coronal synostosis, low frontal hair line, strabismus, ptosis, and partial cutaneous syndactyly of fingers and toes are findings suggestive of the diagnosis of Saethre-Chotzen syndrome. The disease locus was excluded from the two adjacent Saethre-Chotzen candidate regions on 7p by linkage analysis with markers D7S664 and D7S507. This indicates heterogeneity of Saethre-Chotzen syndrome with a locus outside the candidate regions O n 7p.
Who reads Craniosynostosis suggestive of Saethre-Chotzen syndrome: Clinical description of a large kindred and exclusion of candidate regions on 7p?
It is typically read by researchers, students, and practitioners in Biochemistry, Genetics and Molecular Biology.
- Author
- von Gernet, Steven; Schuffenhauer, Simone; Golla, Astrid; Lichtner, Peter; Balg, Stefanie; Mühlbauer, Wolfgang; Murken, Jan; Fairley, Jeffrey; Meitinger, Thomas
- Publisher
- John Wiley and Sons; Wiley (John Wiley & Sons); Wiley-Liss Inc; Wiley (ISSN 0148-7299)
- Published
- 1996
- Language
- EN
- Field
- Biochemistry, Genetics and Molecular Biology (Life Sciences)