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Clinical genetics

Showing results (361-370 of 7,173) with videos related to

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Clinical Genetics|June 16, 2015
Neurofibromatosis type 1 and malignancy in childhoodA Varan, H Şen, B Aydın, et al.
Clinical Genetics|July 20, 2016
Molecular genetic analysis of 30 families with Joubert syndromeT Suzuki, N Miyake, Y Tsurusaki, et al.
Clinical Genetics|December 1, 1982
Homozygous deficiency of C4 in a child with a lupus erythematosus syndromeM Kjellman, A B Laurell, B Löw, et al.
Clinical Genetics|September 1, 1978
Ultrasonography for guidance of amniocentesis in genetic counselingS C Levine, R A Filly, M S Golbus
Clinical Genetics|September 1, 1978
The cloverleaf skullO Yujnovsky, W L Nyhan
Clinical Genetics|February 1, 1983
Myotonic dystrophy: limited electromyographic abnormalities in 2 definite casesS F Sun, E W Streib
Clinical Genetics|June 24, 2015
Hearing loss in Waardenburg syndrome: a systematic reviewJ Song, Y Feng, F R Acke, et al.
Clinical Genetics|September 1, 1980
Prior abortions and neural tube defectsT J David, P A Townley, A R Goldstein
Clinical Genetics|February 1, 1982
Serum cholinesterase in the mothers of neural tube defect progenyS S Lawrie, I Thomson
Clinical Genetics|February 1, 1982
Structural anomalies of the X chromosome: personal observation and review of non-mosaic casesD Wyss, C D DeLozier, J Daniell, et al.
Pageof 718

Showing results (361-370 of 7,173) with videos related to

Sort By:
Pageof 718
Clinical Genetics|June 16, 2015
Neurofibromatosis type 1 and malignancy in childhoodA Varan, H Şen, B Aydın, et al.
Clinical Genetics|July 20, 2016
Molecular genetic analysis of 30 families with Joubert syndromeT Suzuki, N Miyake, Y Tsurusaki, et al.
Clinical Genetics|December 1, 1982
Homozygous deficiency of C4 in a child with a lupus erythematosus syndromeM Kjellman, A B Laurell, B Löw, et al.
Clinical Genetics|September 1, 1978
Ultrasonography for guidance of amniocentesis in genetic counselingS C Levine, R A Filly, M S Golbus
Clinical Genetics|September 1, 1978
The cloverleaf skullO Yujnovsky, W L Nyhan
Clinical Genetics|February 1, 1983
Myotonic dystrophy: limited electromyographic abnormalities in 2 definite casesS F Sun, E W Streib
Clinical Genetics|June 24, 2015
Hearing loss in Waardenburg syndrome: a systematic reviewJ Song, Y Feng, F R Acke, et al.
Clinical Genetics|September 1, 1980
Prior abortions and neural tube defectsT J David, P A Townley, A R Goldstein
Clinical Genetics|February 1, 1982
Serum cholinesterase in the mothers of neural tube defect progenyS S Lawrie, I Thomson
Clinical Genetics|February 1, 1982
Structural anomalies of the X chromosome: personal observation and review of non-mosaic casesD Wyss, C D DeLozier, J Daniell, et al.
Pageof 718