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M Pembrey

Showing results (41-50 of 48) with videos related to

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Clinical Endocrinology|April 1, 1996
Thyroid peroxidase: evidence for disease gene exclusion in Pendred's syndromeE Gausden, J A Armour, B Coyle, et al.
Journal of Medical Genetics|February 1, 1989
The association of Angelman's syndrome with deletions within 15q11-13M Pembrey, S J Fennell, J van den Berghe, et al.
American Journal of Medical Genetics|September 25, 1995
Phenotypic manifestations of branchio-oto-renal syndromeA Chen, M Francis, L Ni, et al.
Human Molecular Genetics|November 5, 1997
IsK and KvLQT1: mutation in either of the two subunits of the slow component of the delayed rectifier potassium channel can cause Jervell and Lange-Nielsen syndromeJ Tyson, L Tranebjaerg, S Bellman, et al.
Human Molecular Genetics|August 1, 1995
Further mutations in Brain 4 (POU3F4) clarify the phenotype in the X-linked deafness, DFN3M Bitner-Glindzicz, P Turnpenny, P Höglund, et al.
American Journal of Medical Genetics|November 15, 2000
Mapping of X chromosome inversion breakpoints [inv(X)(q11q28)] associated with FG syndrome: a second FG locus [FGS2]?S Briault, L Villard, U Rogner, et al.
Lancet (London, England)|July 4, 1998
Recurrence risks in offspring of adults with major heart defects: results from first cohort of British collaborative studyJ Burn, P Brennan, J Little, et al.
American Journal of Medical Genetics|January 31, 1998
A gene for FG syndrome maps in the Xq12-q21.31 regionS Briault, R Hill, A Shrimpton, et al.
Pageof 5

Showing results (41-50 of 48) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 48 results.
Clinical Endocrinology|April 1, 1996
Thyroid peroxidase: evidence for disease gene exclusion in Pendred's syndromeE Gausden, J A Armour, B Coyle, et al.
Journal of Medical Genetics|February 1, 1989
The association of Angelman's syndrome with deletions within 15q11-13M Pembrey, S J Fennell, J van den Berghe, et al.
American Journal of Medical Genetics|September 25, 1995
Phenotypic manifestations of branchio-oto-renal syndromeA Chen, M Francis, L Ni, et al.
Human Molecular Genetics|November 5, 1997
IsK and KvLQT1: mutation in either of the two subunits of the slow component of the delayed rectifier potassium channel can cause Jervell and Lange-Nielsen syndromeJ Tyson, L Tranebjaerg, S Bellman, et al.
Human Molecular Genetics|August 1, 1995
Further mutations in Brain 4 (POU3F4) clarify the phenotype in the X-linked deafness, DFN3M Bitner-Glindzicz, P Turnpenny, P Höglund, et al.
American Journal of Medical Genetics|November 15, 2000
Mapping of X chromosome inversion breakpoints [inv(X)(q11q28)] associated with FG syndrome: a second FG locus [FGS2]?S Briault, L Villard, U Rogner, et al.
Lancet (London, England)|July 4, 1998
Recurrence risks in offspring of adults with major heart defects: results from first cohort of British collaborative studyJ Burn, P Brennan, J Little, et al.
American Journal of Medical Genetics|January 31, 1998
A gene for FG syndrome maps in the Xq12-q21.31 regionS Briault, R Hill, A Shrimpton, et al.
Pageof 5