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W Reardon

Showing results (91-100 of 166) with videos related to

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American Journal of Medical Genetics|August 1, 1992
Five years experience of predictive testing for myotonic dystrophy using linked DNA markersW Reardon, J L Floyd, J Myring, et al.
Neuromuscular Disorders : NMD|January 1, 1992
Molecular analysis for the myotonic dystrophy mutation in neuromuscular disordersJ C MacMillan, J Myring, H G Harley, et al.
The Journal of Clinical Endocrinology and Metabolism|August 12, 1999
Concurrence of Pendred syndrome, autoimmune thyroiditis, and simple goiter in one familyB Vaidya, R Coffey, B Coyle, et al.
Journal of Medical Genetics|October 1, 1989
Central nervous system malformations in Mohr's syndromeW Reardon, M G Harbord, M A Hall-Craggs, et al.
American Journal of Medical Genetics|November 1, 1992
Phenotypic evidence for a common pathogenesis in X-linked deafness pedigrees and in Xq13-q21 deletion related deafnessW Reardon, S Roberts, P D Phelps, et al.
Clinical Genetics|May 1, 1992
Lethal congenital erythroderma: a newly recognised genetic disorderJ P Shield, M R Judge, W Reardon, et al.
Psychoneuroendocrinology|March 14, 2015
Estradiol and cortisol interactions in youth externalizing psychopathologyJennifer L Tackett, Kathleen W Reardon, Kathrin Herzhoff, et al.
Journal of Medical Genetics|August 28, 1999
Prevalence, age of onset, and natural history of thyroid disease in Pendred syndromeW Reardon, R Coffey, T Chowdhury, et al.
Clinical Dysmorphology|August 24, 2000
An unknown combination of infantile spasms, retinal lesions, facial dysmorphism and limb abnormalitiesA S Plomp, W Reardon, S Benton, et al.
American Journal of Medical Genetics|August 1, 1994
Autosomal recessive congenital intrauterine infection-like syndrome of microcephaly, intracranial calcification, and CNS diseaseW Reardon, A Hockey, P Silberstein, et al.
Pageof 17

Showing results (91-100 of 166) with videos related to

Sort By:
Pageof 17
American Journal of Medical Genetics|August 1, 1992
Five years experience of predictive testing for myotonic dystrophy using linked DNA markersW Reardon, J L Floyd, J Myring, et al.
Neuromuscular Disorders : NMD|January 1, 1992
Molecular analysis for the myotonic dystrophy mutation in neuromuscular disordersJ C MacMillan, J Myring, H G Harley, et al.
The Journal of Clinical Endocrinology and Metabolism|August 12, 1999
Concurrence of Pendred syndrome, autoimmune thyroiditis, and simple goiter in one familyB Vaidya, R Coffey, B Coyle, et al.
Journal of Medical Genetics|October 1, 1989
Central nervous system malformations in Mohr's syndromeW Reardon, M G Harbord, M A Hall-Craggs, et al.
American Journal of Medical Genetics|November 1, 1992
Phenotypic evidence for a common pathogenesis in X-linked deafness pedigrees and in Xq13-q21 deletion related deafnessW Reardon, S Roberts, P D Phelps, et al.
Clinical Genetics|May 1, 1992
Lethal congenital erythroderma: a newly recognised genetic disorderJ P Shield, M R Judge, W Reardon, et al.
Psychoneuroendocrinology|March 14, 2015
Estradiol and cortisol interactions in youth externalizing psychopathologyJennifer L Tackett, Kathleen W Reardon, Kathrin Herzhoff, et al.
Journal of Medical Genetics|August 28, 1999
Prevalence, age of onset, and natural history of thyroid disease in Pendred syndromeW Reardon, R Coffey, T Chowdhury, et al.
Clinical Dysmorphology|August 24, 2000
An unknown combination of infantile spasms, retinal lesions, facial dysmorphism and limb abnormalitiesA S Plomp, W Reardon, S Benton, et al.
American Journal of Medical Genetics|August 1, 1994
Autosomal recessive congenital intrauterine infection-like syndrome of microcephaly, intracranial calcification, and CNS diseaseW Reardon, A Hockey, P Silberstein, et al.
Pageof 17