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A C Berry

Showing results (51-60 of 58) with videos related to

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Clinical Genetics|October 1, 1988
PRUFILE: a clinical and laboratory database for the genetics centreD E Mutton, K Chown, L Thomson, et al.
Journal of Medical Genetics|October 1, 1991
A new form of autosomal dominant arthrogryposisM M Lai, M A Tettenborn, J G Hall, et al.
Journal of Medical Genetics|March 1, 1989
Spontaneous and induced chromosome breakage in chorionic villus samples: a cytogenetic approach to first trimester prenatal diagnosis of ataxia telangiectasia syndromeJ Llerena, M Murer-Orlando, M McGuire, et al.
Journal of Medical Genetics|July 1, 1995
A fetus with an X;1 balanced reciprocal translocation and eye diseaseM J Seller, K Pal, S Horsley, et al.
Epidemiology and Infection|March 15, 2019
Online symptom checker diagnostic and triage accuracy for HIV and hepatitis CA C Berry, B D Cash, B Wang, et al.
Human Molecular Genetics|August 1, 1995
A nonsense mutation of the human luteinizing hormone receptor gene in Leydig cell hypoplasiaL Laue, S M Wu, M Kudo, et al.
Molecular Endocrinology (Baltimore, Md.)|November 17, 1998
Inactivation of the luteinizing hormone/chorionic gonadotropin receptor by an insertional mutation in Leydig cell hypoplasiaS M Wu, K M Hallermeier, L Laue, et al.
Journal of Medical Genetics|June 1, 1979
Sixteen years' experience of counselling, diagnosis, and prenatal detection in one genetic centre: progress, results, and problemsP E Polani, E Alberman, B J Alexander, et al.
Pageof 6

Showing results (51-60 of 58) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 58 results.
Clinical Genetics|October 1, 1988
PRUFILE: a clinical and laboratory database for the genetics centreD E Mutton, K Chown, L Thomson, et al.
Journal of Medical Genetics|October 1, 1991
A new form of autosomal dominant arthrogryposisM M Lai, M A Tettenborn, J G Hall, et al.
Journal of Medical Genetics|March 1, 1989
Spontaneous and induced chromosome breakage in chorionic villus samples: a cytogenetic approach to first trimester prenatal diagnosis of ataxia telangiectasia syndromeJ Llerena, M Murer-Orlando, M McGuire, et al.
Journal of Medical Genetics|July 1, 1995
A fetus with an X;1 balanced reciprocal translocation and eye diseaseM J Seller, K Pal, S Horsley, et al.
Epidemiology and Infection|March 15, 2019
Online symptom checker diagnostic and triage accuracy for HIV and hepatitis CA C Berry, B D Cash, B Wang, et al.
Human Molecular Genetics|August 1, 1995
A nonsense mutation of the human luteinizing hormone receptor gene in Leydig cell hypoplasiaL Laue, S M Wu, M Kudo, et al.
Molecular Endocrinology (Baltimore, Md.)|November 17, 1998
Inactivation of the luteinizing hormone/chorionic gonadotropin receptor by an insertional mutation in Leydig cell hypoplasiaS M Wu, K M Hallermeier, L Laue, et al.
Journal of Medical Genetics|June 1, 1979
Sixteen years' experience of counselling, diagnosis, and prenatal detection in one genetic centre: progress, results, and problemsP E Polani, E Alberman, B J Alexander, et al.
Pageof 6