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K D Mathews

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The Journal of Bone and Joint Surgery. American Volume|October 1, 1996
Update on the genetic bases of disorders with orthopaedic manifestationsF R Dietz, K D Mathews
Current Opinion in Neurology|October 1, 1996
The molecular genetics of human facioscapulohumeral muscular dystrophy and the myodystrophy mouse modelK D Mathews, K A Mills
Journal of Child Neurology|May 1, 1996
Hypertensive encephalopathy in childhoodR R Wright, K D Mathews
Mammalian Genome : Official Journal of the International Mammalian Genome Society|September 1, 1996
The Ant1 gene maps near Klk3 on proximal mouse chromosome 8K A Mills, J W Ellison, K D Mathews
American Journal of Medical Genetics|December 1, 1989
Börjeson-Forssman-Lehmann syndrome localizationK D Mathews, K Buetow, G Turner, et al.
Journal of Child Neurology|July 1, 1989
Autosomal recessive cerebellar hypoplasiaK D Mathews, A K Afifi, J W Hanson
Clinical Orthopaedics and Related Research|September 1, 1990
Reflex sympathetic dystrophy in childrenF R Dietz, K D Mathews, W J Montgomery
Mammalian Genome : Official Journal of the International Mammalian Genome Society|September 1, 1995
A syntrophin gene maps to mouse chromosome 8 and is not the myodystrophy geneK A Mills, Y Sunada, K P Campbell, et al.
Neurology|May 24, 2000
FSH dystrophy 4q35 deletion in patients presenting with facial-sparing scapular myopathyK J Felice, W A North, S A Moore, et al.
Muscle & Nerve. Supplement|April 12, 2013
Mouse myodystrophy (myd) mutation: refined mapping in an interval flanked by homology with distal human 4qK D Mathews, K A Mills, H L Bailey, et al.
Pageof 3

Showing results (1-10 of 22) with videos related to

Sort By:
Pageof 3
The Journal of Bone and Joint Surgery. American Volume|October 1, 1996
Update on the genetic bases of disorders with orthopaedic manifestationsF R Dietz, K D Mathews
Current Opinion in Neurology|October 1, 1996
The molecular genetics of human facioscapulohumeral muscular dystrophy and the myodystrophy mouse modelK D Mathews, K A Mills
Journal of Child Neurology|May 1, 1996
Hypertensive encephalopathy in childhoodR R Wright, K D Mathews
Mammalian Genome : Official Journal of the International Mammalian Genome Society|September 1, 1996
The Ant1 gene maps near Klk3 on proximal mouse chromosome 8K A Mills, J W Ellison, K D Mathews
American Journal of Medical Genetics|December 1, 1989
Börjeson-Forssman-Lehmann syndrome localizationK D Mathews, K Buetow, G Turner, et al.
Journal of Child Neurology|July 1, 1989
Autosomal recessive cerebellar hypoplasiaK D Mathews, A K Afifi, J W Hanson
Clinical Orthopaedics and Related Research|September 1, 1990
Reflex sympathetic dystrophy in childrenF R Dietz, K D Mathews, W J Montgomery
Mammalian Genome : Official Journal of the International Mammalian Genome Society|September 1, 1995
A syntrophin gene maps to mouse chromosome 8 and is not the myodystrophy geneK A Mills, Y Sunada, K P Campbell, et al.
Neurology|May 24, 2000
FSH dystrophy 4q35 deletion in patients presenting with facial-sparing scapular myopathyK J Felice, W A North, S A Moore, et al.
Muscle & Nerve. Supplement|April 12, 2013
Mouse myodystrophy (myd) mutation: refined mapping in an interval flanked by homology with distal human 4qK D Mathews, K A Mills, H L Bailey, et al.
Pageof 3