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Diabetes & Metabolism|May 4, 2013
A novel GATA6 mutation leading to congenital heart defects and permanent neonatal diabetes: a case reportG Catli, A Abaci, S E Flanagan, et al.
Biochemical Genetics|January 9, 2016
Association Between Vitamin D Receptor Polymorphism and Familial Mediterranean Fever Disease in Turkish ChildrenS Kizildag, F Dedemoglu, A Anik, et al.
Genomics|June 1, 1990
Human embryonic/atrial myosin alkali light chain gene: characterization, sequence, and chromosomal locationJ Seharaseyon, E Bober, C L Hsieh, et al.
Development (Cambridge, England)|November 1, 1994
Initial steps of myogenesis in somites are independent of influence from axial structuresE Bober, B Brand-Saberi, C Ebensperger, et al.
Nucleic Acids Research|November 11, 1990
A highly conserved enhancer downstream of the human MLC1/3 locus is a target for multiple myogenic determination factorsN Rosenthal, E B Berglund, B M Wentworth, et al.
Gene|June 15, 1988
Alkali myosin light chains in man are encoded by a multigene family that includes the adult skeletal muscle, the embryonic or atrial, and nonsarcomeric isoformsU Seidel, E Bober, B Winter, et al.
Development (Cambridge, England)|August 6, 1999
Craniofacial, vestibular and bone defects in mice lacking the Distal-less-related gene Dlx5D Acampora, G R Merlo, L Paleari, et al.
British Journal of Cancer|December 1, 1991
Expression of members of the myf gene family in human rhabdomyosarcomasJ Clark, P J Rocques, T Braun, et al.
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