B B A de Vries - JoVE Visualize

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Nederlands Tijdschrift Voor Geneeskunde|November 26, 2008

[Sudden blindness: consider Leber's hereditary optic neuropathy]J H Schieving, B B A de Vries, F Hol, et al.

Journal of Medical Genetics|June 17, 2003

Telomeres: a diagnosis at the end of the chromosomesB B A De Vries, R Winter, A Schinzel, et al.

American Journal of Medical Genetics. Part A|November 4, 2024

Cyclic Vomiting Syndrome in Patients Affected by Jansen-de Vries Syndrome: Results From an International SurveyA Pizzol, K A Adams, B B A de Vries, et al.

Psychopathology|July 28, 2007

Klinefelter's syndrome and Prader-Willi syndrome: a rare combinationW M A Verhoeven, B B A de Vries, S J H Duffels, et al.

Molecular Syndromology|July 24, 2012

A 380-kb Duplication in 7p22.3 Encompassing the LFNG Gene in a Boy with Asperger SyndromeA T Vulto-van Silfhout, A F M de Brouwer, N de Leeuw, et al.

Clinical Genetics|October 10, 2002

A new case of dup(3q) syndrome due to a pure duplication of 3qterB H W Faas, B B A De Vries, J Van Es-Van Gaal, et al.

Clinical Genetics|June 26, 2002

De novo MECP2 frameshift mutation in a boy with moderate mental retardation, obesity and gynaecomastiaT Kleefstra, H G Yntema, A R Oudakker, et al.

Neurology|August 28, 2002

Clinical and genetic heterogeneity in benign hereditary choreaG J Breedveld, A K Percy, M E MacDonald, et al.

Clinical Genetics|September 14, 2007

Pure subtelomeric microduplications as a cause of mental retardationE M Ruiter, D A Koolen, T Kleefstra, et al.

Clinical Genetics|January 12, 2016

De novo loss-of-function mutations in X-linked SMC1A cause severe ID and therapy-resistant epilepsy in females: expanding the phenotypic spectrumS Jansen, T Kleefstra, M H Willemsen, et al.

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Showing results (1-10 of 31) with videos related to

Sort By:

Pageof 4

Nederlands Tijdschrift Voor Geneeskunde|November 26, 2008

[Sudden blindness: consider Leber's hereditary optic neuropathy]J H Schieving, B B A de Vries, F Hol, et al.

Journal of Medical Genetics|June 17, 2003

Telomeres: a diagnosis at the end of the chromosomesB B A De Vries, R Winter, A Schinzel, et al.

American Journal of Medical Genetics. Part A|November 4, 2024

Cyclic Vomiting Syndrome in Patients Affected by Jansen-de Vries Syndrome: Results From an International SurveyA Pizzol, K A Adams, B B A de Vries, et al.

Psychopathology|July 28, 2007

Klinefelter's syndrome and Prader-Willi syndrome: a rare combinationW M A Verhoeven, B B A de Vries, S J H Duffels, et al.

Molecular Syndromology|July 24, 2012

A 380-kb Duplication in 7p22.3 Encompassing the LFNG Gene in a Boy with Asperger SyndromeA T Vulto-van Silfhout, A F M de Brouwer, N de Leeuw, et al.

Clinical Genetics|October 10, 2002

A new case of dup(3q) syndrome due to a pure duplication of 3qterB H W Faas, B B A De Vries, J Van Es-Van Gaal, et al.

Clinical Genetics|June 26, 2002

De novo MECP2 frameshift mutation in a boy with moderate mental retardation, obesity and gynaecomastiaT Kleefstra, H G Yntema, A R Oudakker, et al.

Neurology|August 28, 2002

Clinical and genetic heterogeneity in benign hereditary choreaG J Breedveld, A K Percy, M E MacDonald, et al.

Clinical Genetics|September 14, 2007

Pure subtelomeric microduplications as a cause of mental retardationE M Ruiter, D A Koolen, T Kleefstra, et al.

Clinical Genetics|January 12, 2016

De novo loss-of-function mutations in X-linked SMC1A cause severe ID and therapy-resistant epilepsy in females: expanding the phenotypic spectrumS Jansen, T Kleefstra, M H Willemsen, et al.

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