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Anne M Slavotinek

Showing results (11-20 of 93) with videos related to

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Clinical Dysmorphology|October 18, 2003
Large interstitial deletion of chromosome 13q and severe short stature: clinical report and review of the literatureAnne M Slavotinek, Felicitas Lacbawan
American Journal of Medical Genetics. Part A|June 11, 2020
Going forward in a new worldAnne M Slavotinek, Benjamin D Solomon
American Journal of Medical Genetics. Part A|July 24, 2020
Announcing a new manuscript category for the American Journal of Medical Genetics Part A: Dispatches from BiotechBenjamin D Solomon, Anne M Slavotinek
Clinical Dysmorphology|October 18, 2003
A female infant with duplication of chromosome 2q33 to 2q37.3Anne M Slavotinek, Debra Boles, Felicitas Lacbawan
American Journal of Medical Genetics. Part A|August 6, 2003
Non-syndromic hemihyperplasia in a male and his motherAnne M Slavotinek, Michael T Collins, Maximilian Muenke
Clinical Dysmorphology|December 13, 2006
Oculo-ectodermal syndrome: is arachnoid cyst a common finding?Madelena M Martin, Tai Lockspieler, Anne M Slavotinek
American Journal of Medical Genetics. Part A|March 29, 2005
Fryns syndrome with osteochondrodysplasiaAnne M Slavotinek, H Robinson, M A Steele
American Journal of Medical Genetics. Part A|December 31, 2003
Segregation of a t(1;3) translocation in multiple affected family members with both types of adjacent-1 segregantsChahira Kozma, Anne M Slavotinek, Jeanne M Meck
Developmental Biology|August 31, 2014
The FgfrL1 receptor is required for development of slow muscle fibersRuth Amann, Stefan Wyder, Anne M Slavotinek, et al.
American Journal of Medical Genetics. Part A|August 13, 2008
Clinical and molecular studies of patients with characteristics of Opitz G/BBB syndrome shows a novel MID1 mutationElena W Y Hsieh, Karin Vargervik, Anne M Slavotinek
Pageof 10

Showing results (11-20 of 93) with videos related to

Sort By:
Pageof 10
Clinical Dysmorphology|October 18, 2003
Large interstitial deletion of chromosome 13q and severe short stature: clinical report and review of the literatureAnne M Slavotinek, Felicitas Lacbawan
American Journal of Medical Genetics. Part A|June 11, 2020
Going forward in a new worldAnne M Slavotinek, Benjamin D Solomon
American Journal of Medical Genetics. Part A|July 24, 2020
Announcing a new manuscript category for the American Journal of Medical Genetics Part A: Dispatches from BiotechBenjamin D Solomon, Anne M Slavotinek
Clinical Dysmorphology|October 18, 2003
A female infant with duplication of chromosome 2q33 to 2q37.3Anne M Slavotinek, Debra Boles, Felicitas Lacbawan
American Journal of Medical Genetics. Part A|August 6, 2003
Non-syndromic hemihyperplasia in a male and his motherAnne M Slavotinek, Michael T Collins, Maximilian Muenke
Clinical Dysmorphology|December 13, 2006
Oculo-ectodermal syndrome: is arachnoid cyst a common finding?Madelena M Martin, Tai Lockspieler, Anne M Slavotinek
American Journal of Medical Genetics. Part A|March 29, 2005
Fryns syndrome with osteochondrodysplasiaAnne M Slavotinek, H Robinson, M A Steele
American Journal of Medical Genetics. Part A|December 31, 2003
Segregation of a t(1;3) translocation in multiple affected family members with both types of adjacent-1 segregantsChahira Kozma, Anne M Slavotinek, Jeanne M Meck
Developmental Biology|August 31, 2014
The FgfrL1 receptor is required for development of slow muscle fibersRuth Amann, Stefan Wyder, Anne M Slavotinek, et al.
American Journal of Medical Genetics. Part A|August 13, 2008
Clinical and molecular studies of patients with characteristics of Opitz G/BBB syndrome shows a novel MID1 mutationElena W Y Hsieh, Karin Vargervik, Anne M Slavotinek
Pageof 10