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The British Journal of Ophthalmology
|
September 1, 1993
Cataract and myotonic dystrophy: the role of molecular diagnosis
W Reardon, J C MacMillan, J Myring, et al.
Perspectives on Psychological Science : a Journal of the Association for Psychological Science
|
November 9, 2022
Understanding the Leaders of Tomorrow: The Need to Study Leadership in Adolescence
Jennifer L Tackett, Kathleen W Reardon, Nathanael J Fast, et al.
International Journal of Audiology
|
March 19, 2003
Neuro-otological findings in Pendred syndrome
L M Luxon, M Cohen, R A Coffey, et al.
Nature Genetics
|
April 1, 1996
Pendred syndrome (goitre and sensorineural hearing loss) maps to chromosome 7 in the region containing the nonsyndromic deafness gene DFNB4
B Coyle, R Coffey, J A Armour, et al.
Clinical Endocrinology
|
April 1, 1996
Thyroid peroxidase: evidence for disease gene exclusion in Pendred's syndrome
E Gausden, J A Armour, B Coyle, et al.
American Journal of Medical Genetics
|
October 1, 1993
Mesomelic limb shortness: a previously unreported autosomal recessive type
W Reardon, C M Hall, S Slaney, et al.
Human Molecular Genetics
|
August 1, 1994
Localization of the genetic locus for Saethre-Chotzen syndrome to a 6 cM region of chromosome 7 using four cases with apparently balanced translocations at 7p21.2
C S Rose, A A King, D Summers, et al.
QJM : Monthly Journal of the Association of Physicians
|
July 1, 1997
Pendred syndrome--100 years of underascertainment?
W Reardon, R Coffey, P D Phelps, et al.
British Journal of Audiology
|
April 1, 1992
Clinical and genetic heterogeneity in X-linked deafness
W Reardon, H R Middleton-Price, S Malcolm, et al.
American Journal of Medical Genetics. Part A
|
February 12, 2009
Aplasia of cochlear nerves and olfactory bulbs in association with SOX10 mutation
C P Barnett, R Mendoza-Londono, S Blaser, et al.
Page
of 17
Search research articles
Search
Showing results (111-120 of 166) with videos related to
Sort By:
Page
of 17
The British Journal of Ophthalmology
|
September 1, 1993
Cataract and myotonic dystrophy: the role of molecular diagnosis
W Reardon, J C MacMillan, J Myring, et al.
Perspectives on Psychological Science : a Journal of the Association for Psychological Science
|
November 9, 2022
Understanding the Leaders of Tomorrow: The Need to Study Leadership in Adolescence
Jennifer L Tackett, Kathleen W Reardon, Nathanael J Fast, et al.
International Journal of Audiology
|
March 19, 2003
Neuro-otological findings in Pendred syndrome
L M Luxon, M Cohen, R A Coffey, et al.
Nature Genetics
|
April 1, 1996
Pendred syndrome (goitre and sensorineural hearing loss) maps to chromosome 7 in the region containing the nonsyndromic deafness gene DFNB4
B Coyle, R Coffey, J A Armour, et al.
Clinical Endocrinology
|
April 1, 1996
Thyroid peroxidase: evidence for disease gene exclusion in Pendred's syndrome
E Gausden, J A Armour, B Coyle, et al.
American Journal of Medical Genetics
|
October 1, 1993
Mesomelic limb shortness: a previously unreported autosomal recessive type
W Reardon, C M Hall, S Slaney, et al.
Human Molecular Genetics
|
August 1, 1994
Localization of the genetic locus for Saethre-Chotzen syndrome to a 6 cM region of chromosome 7 using four cases with apparently balanced translocations at 7p21.2
C S Rose, A A King, D Summers, et al.
QJM : Monthly Journal of the Association of Physicians
|
July 1, 1997
Pendred syndrome--100 years of underascertainment?
W Reardon, R Coffey, P D Phelps, et al.
British Journal of Audiology
|
April 1, 1992
Clinical and genetic heterogeneity in X-linked deafness
W Reardon, H R Middleton-Price, S Malcolm, et al.
American Journal of Medical Genetics. Part A
|
February 12, 2009
Aplasia of cochlear nerves and olfactory bulbs in association with SOX10 mutation
C P Barnett, R Mendoza-Londono, S Blaser, et al.
Page
of 17