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Clinical genetics

Showing results (321-330 of 7,173) with videos related to

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Clinical Genetics|July 1, 1987
Proximal duplication of the long arm of chromosome 10 (10q11.2----10q22): a distinct clinical entityJ P Fryns, A Kleczkowska, L Igodt-Ameye, et al.
Clinical Genetics|April 1, 1988
Verbal deficits in Klinefelter (XXY) adults living in the communityM E Porter, H A Gardner, P DeFeudis, et al.
Clinical Genetics|April 1, 1988
HLA determinants in 70 Danish patients with idiopathic haemochromatosisN Milman, N Graudal, L S Nielsen, et al.
Clinical Genetics|November 25, 2018
A HS6ST2 gene variant associated with X-linked intellectual disability and severe myopia in two male twinsLeda Paganini, Loubna A Hadi, Massimiliano Chetta, et al.
Clinical Genetics|January 14, 2021
Fragile X premutation and associated health conditions: A reviewNattaporn Tassanakijpanich, Randi J Hagerman, Juthamas Worachotekamjorn
Clinical Genetics|March 1, 2021
Genetic and phenotypic analysis of 101 patients with developmental delay or intellectual disability using whole-exome sequencingTakuya Hiraide, Kaori Yamoto, Yohei Masunaga, et al.
Clinical Genetics|December 8, 2016
Facial dysmorphism is influenced by ethnic background of the patient and of the evaluatorA Lumaka, N Cosemans, A Lulebo Mampasi, et al.
Clinical Genetics|February 14, 2017
Mutations of MYH14 are associated to anorectal malformations with recto-perineal fistulas in a small subset of Chinese populationZhongxian Zhu, Lei Peng, Guanglin Chen, et al.
Clinical Genetics|April 12, 2017
Patient understanding of genetic information influences reproductive decision making in retinoblastomaA Foster, L Boyes, L Burgess, et al.
Clinical Genetics|November 29, 2021
Mitochondrial developmental encephalopathy with bilateral optic neuropathy related to homozygous variants in IMMT geneAna Victoria Marco-Hernández, Miguel Tomás-Vila, Alejandro Montoya-Filardi, et al.
Pageof 718

Showing results (321-330 of 7,173) with videos related to

Sort By:
Pageof 718
Clinical Genetics|July 1, 1987
Proximal duplication of the long arm of chromosome 10 (10q11.2----10q22): a distinct clinical entityJ P Fryns, A Kleczkowska, L Igodt-Ameye, et al.
Clinical Genetics|April 1, 1988
Verbal deficits in Klinefelter (XXY) adults living in the communityM E Porter, H A Gardner, P DeFeudis, et al.
Clinical Genetics|April 1, 1988
HLA determinants in 70 Danish patients with idiopathic haemochromatosisN Milman, N Graudal, L S Nielsen, et al.
Clinical Genetics|November 25, 2018
A HS6ST2 gene variant associated with X-linked intellectual disability and severe myopia in two male twinsLeda Paganini, Loubna A Hadi, Massimiliano Chetta, et al.
Clinical Genetics|January 14, 2021
Fragile X premutation and associated health conditions: A reviewNattaporn Tassanakijpanich, Randi J Hagerman, Juthamas Worachotekamjorn
Clinical Genetics|March 1, 2021
Genetic and phenotypic analysis of 101 patients with developmental delay or intellectual disability using whole-exome sequencingTakuya Hiraide, Kaori Yamoto, Yohei Masunaga, et al.
Clinical Genetics|December 8, 2016
Facial dysmorphism is influenced by ethnic background of the patient and of the evaluatorA Lumaka, N Cosemans, A Lulebo Mampasi, et al.
Clinical Genetics|February 14, 2017
Mutations of MYH14 are associated to anorectal malformations with recto-perineal fistulas in a small subset of Chinese populationZhongxian Zhu, Lei Peng, Guanglin Chen, et al.
Clinical Genetics|April 12, 2017
Patient understanding of genetic information influences reproductive decision making in retinoblastomaA Foster, L Boyes, L Burgess, et al.
Clinical Genetics|November 29, 2021
Mitochondrial developmental encephalopathy with bilateral optic neuropathy related to homozygous variants in IMMT geneAna Victoria Marco-Hernández, Miguel Tomás-Vila, Alejandro Montoya-Filardi, et al.
Pageof 718