The synpolydactyly homolog (spdh) mutation in the mouse – a defect in patterning and growth of limb cartilage elements
Author:
Publisher
Elsevier BV
Subject
Developmental Biology,Embryology
Reference47 articles.
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2. Short GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophy;Brais;Nat. Genet.,1998
3. The mouse hoxd13(spdh) mutation, a polyalanine expansion similar to human type II synpolydactyly (spd), disrupts the function but not the expression of other hoxd genes;Bruneau;Dev. Biol.,2001
4. Noggin, cartilage morphogenesis, and joint formation in the mammalian skeleton;Brunet;Science,1998
5. Polydactylous limbs in Strong's Luxoimice result from ectopic polarizing activity;Chan;Development,1995
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