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Sheila Unger

Showing results (11-20 of 141) with videos related to

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American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|July 14, 2012
New topics in the skeletal dysplasiasSheila Unger, Luisa Bonafé, Andrea Superti-Furga
BMJ Case Reports|September 2, 2015
Stuve-Wiedemann syndrome with a novel mutationMegan Knipe, Rowan Stanbury, Sheila Unger, et al.
European Journal of Medical Genetics|March 6, 2012
Clinical and radiological findings in Pallister-Killian syndromeSaumya Jamuar, Angeline Lai, Sheila Unger, et al.
American Journal of Medical Genetics. Part A|June 12, 2025
De Novo SLC12A2 Variant Presenting as Congenital Hearing Loss With Vestibular AreflexiaKatja Ludin, Anna M Kopps, Celine Richard, et al.
Pediatric Radiology|December 6, 2005
Petrified ears in a patient with Keutel syndrome: temporal bone CT findingsHemant Parmar, Susan Blaser, Sheila Unger, et al.
Revue Medicale Suisse|March 22, 2012
[New therapies for children affected by bone diseases]Diana Ballhausen, Nuria Garcia Dépraz, Ilse Kern, et al.
Revue Medicale Suisse|July 19, 2016
[BRCA mutations: from Angelina Jolie to specific therapies]Veronica Aedo Lopez, Athina Stravodimou, Sheila Unger, et al.
Revue Medicale Suisse|February 14, 2025
[Experience of a support group for women carrying BRCA1/2 mutations]Déborah Hersch-Bitter, Yann Lurton, Camille Kumps, et al.
American Journal of Medical Genetics. Part A|January 12, 2021
Cancer surveillance in children with Ollier Disease and Maffucci SyndromeManuel Diezi, Pierre-Yves Zambelli, Andrea Superti-Furga, et al.
European Journal of Pediatrics|November 9, 2002
Severe cleidocranial dysplasia can mimic hypophosphatasiaSheila Unger, Etienne Mornet, Stefan Mundlos, et al.
Pageof 15

Showing results (11-20 of 141) with videos related to

Sort By:
Pageof 15
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|July 14, 2012
New topics in the skeletal dysplasiasSheila Unger, Luisa Bonafé, Andrea Superti-Furga
BMJ Case Reports|September 2, 2015
Stuve-Wiedemann syndrome with a novel mutationMegan Knipe, Rowan Stanbury, Sheila Unger, et al.
European Journal of Medical Genetics|March 6, 2012
Clinical and radiological findings in Pallister-Killian syndromeSaumya Jamuar, Angeline Lai, Sheila Unger, et al.
American Journal of Medical Genetics. Part A|June 12, 2025
De Novo SLC12A2 Variant Presenting as Congenital Hearing Loss With Vestibular AreflexiaKatja Ludin, Anna M Kopps, Celine Richard, et al.
Pediatric Radiology|December 6, 2005
Petrified ears in a patient with Keutel syndrome: temporal bone CT findingsHemant Parmar, Susan Blaser, Sheila Unger, et al.
Revue Medicale Suisse|March 22, 2012
[New therapies for children affected by bone diseases]Diana Ballhausen, Nuria Garcia Dépraz, Ilse Kern, et al.
Revue Medicale Suisse|July 19, 2016
[BRCA mutations: from Angelina Jolie to specific therapies]Veronica Aedo Lopez, Athina Stravodimou, Sheila Unger, et al.
Revue Medicale Suisse|February 14, 2025
[Experience of a support group for women carrying BRCA1/2 mutations]Déborah Hersch-Bitter, Yann Lurton, Camille Kumps, et al.
American Journal of Medical Genetics. Part A|January 12, 2021
Cancer surveillance in children with Ollier Disease and Maffucci SyndromeManuel Diezi, Pierre-Yves Zambelli, Andrea Superti-Furga, et al.
European Journal of Pediatrics|November 9, 2002
Severe cleidocranial dysplasia can mimic hypophosphatasiaSheila Unger, Etienne Mornet, Stefan Mundlos, et al.
Pageof 15