𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Autosomal dominant transmission of nonsyndromic diastasis recti and weakness of the linea alba

✍ Scribed by M.Cristina Digilio; Rossella Capolino; Bruno Dallapiccola


Book ID
101454203
Publisher
John Wiley and Sons
Year
2007
Tongue
English
Weight
99 KB
Volume
146A
Category
Article
ISSN
1552-4825

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


DFNA8/12 caused by TECTA mutations is th
✍ Michael S. Hildebrand; MatΓ­as MorΓ­n; Nicole C. Meyer; Fernando Mayo; Silvia Moda πŸ“‚ Article πŸ“… 2011 πŸ› John Wiley and Sons 🌐 English βš– 476 KB

The prevalence of DFNA8/DFNA12 (DFNA8/12), a type of autosomal dominant nonsyndromic hearing loss (ADNSHL), is unknown as comprehensive population-based genetic screening has not been conducted. We therefore completed unbiased screening for TECTA mutations in a Spanish cohort of 372 probands from AD

Analysis of 31 families with an apparent
✍ Ulrich, Vibeke; Russell, Michael BjΓΈrn; Østergaard, Steen; Olesen, Jes πŸ“‚ Article πŸ“… 1997 πŸ› John Wiley and Sons 🌐 English βš– 15 KB πŸ‘ 2 views

We analyzed 31 families selected for an apparently autosomal-dominant mode of inheritance of migraine with aura (MA) in the nuclear family. The nuclear families were expanded with first-and second-degree relatives. All interviews were made by physicians experienced in headache diagnoses. The criteri