Werner mesomelic syndrome (WMS) is an autosomal dominant disorder with unknown molecular etiology characterized by hypo-or aplasia of the tibiae in addition to the preaxial polydactyly (PPD) of the hands and feet and/or five-fingered hand with absence of thumbs. We show that point mutations of a spe
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Bilateral complete polysyndactyly (type IV Haas)
โ Scribed by Gillessen-Kaesbach, Gabriele ;Majewski, F.
- Publisher
- John Wiley and Sons
- Year
- 1991
- Tongue
- English
- Weight
- 274 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0148-7299
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## Background: In the mouse model of complete transposition of the great arteries (tga) produced by all-trans retinoic acid (ra), parietal and septal ridges in the outflow tract (ot) are hypoplastic. at first, these ridges are generated by an expanded cardiac jelly (mainly myocardial basement membr