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Angelika J Dawson

Showing results (1-10 of 14) with videos related to

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The New England Journal of Medicine|February 25, 2011
Recurrent miscarriageBernard N Chodirker, Angelika J Dawson
Case Reports in Genetics|June 12, 2015
PWS/AS MS-MLPA Confirms Maternal Origin of 15q11.2 MicroduplicationAngelika J Dawson, Janice Cox, Karine Hovanes, et al.
Journal of Medical Genetics|November 17, 2020
Canadian College of Medical Geneticists (CCMG) points to consider: resuming genetic services in a pandemic-a summaryLauren Chad, Angelika J Dawson, Elaine Suk-Ying Goh
Journal of Child Neurology|March 29, 2006
Congenital indifference to pain and deletion of chromosome 10q-: new associationCharuta Joshi, Angelika J Dawson, Shannon R Sanders, et al.
Clinical Dysmorphology|April 2, 2004
Severe hemihypotrophy in a female infant with mosaic Turner syndrome: a variant of Russell-Silver syndrome?Chumei C Li, Bernard N Chodirker, Angelika J Dawson, et al.
American Journal of Medical Genetics. Part A|April 28, 2015
Ataxia-telangiectasia with female fertilityAngelika J Dawson, Sandra Marles, Michelle Tomiuk, et al.
Molecular Genetics & Genomic Medicine|August 1, 2014
A-TWinnipeg: Pathogenesis of rare ATM missense mutation c.6200C>A with decreased protein expression and downstream signaling, early-onset dystonia, cancer, and life-threatening radiotoxicityKotoka Nakamura, Francesca Fike, Sara Haghayegh, et al.
American Journal of Medical Genetics. Part A|November 15, 2006
Unusual dicentric chromosome 22 associated with a 22q13 deletionTina Babineau, Heather L Wilson, Angelika J Dawson, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|February 19, 2014
Chromosome microarray and undiagnosed seizures in a pediatric patientAngelika J Dawson, Aizeddin A Mhanni, Frances A Booth, et al.
Clinical Dysmorphology|October 10, 2020
Heterozygous intragenic deletions of FREM1 are not associated with trigonocephalyAngelika J Dawson, Karine Hovanes, Jing Liu, et al.
Pageof 2

Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
The New England Journal of Medicine|February 25, 2011
Recurrent miscarriageBernard N Chodirker, Angelika J Dawson
Case Reports in Genetics|June 12, 2015
PWS/AS MS-MLPA Confirms Maternal Origin of 15q11.2 MicroduplicationAngelika J Dawson, Janice Cox, Karine Hovanes, et al.
Journal of Medical Genetics|November 17, 2020
Canadian College of Medical Geneticists (CCMG) points to consider: resuming genetic services in a pandemic-a summaryLauren Chad, Angelika J Dawson, Elaine Suk-Ying Goh
Journal of Child Neurology|March 29, 2006
Congenital indifference to pain and deletion of chromosome 10q-: new associationCharuta Joshi, Angelika J Dawson, Shannon R Sanders, et al.
Clinical Dysmorphology|April 2, 2004
Severe hemihypotrophy in a female infant with mosaic Turner syndrome: a variant of Russell-Silver syndrome?Chumei C Li, Bernard N Chodirker, Angelika J Dawson, et al.
American Journal of Medical Genetics. Part A|April 28, 2015
Ataxia-telangiectasia with female fertilityAngelika J Dawson, Sandra Marles, Michelle Tomiuk, et al.
Molecular Genetics & Genomic Medicine|August 1, 2014
A-TWinnipeg: Pathogenesis of rare ATM missense mutation c.6200C>A with decreased protein expression and downstream signaling, early-onset dystonia, cancer, and life-threatening radiotoxicityKotoka Nakamura, Francesca Fike, Sara Haghayegh, et al.
American Journal of Medical Genetics. Part A|November 15, 2006
Unusual dicentric chromosome 22 associated with a 22q13 deletionTina Babineau, Heather L Wilson, Angelika J Dawson, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|February 19, 2014
Chromosome microarray and undiagnosed seizures in a pediatric patientAngelika J Dawson, Aizeddin A Mhanni, Frances A Booth, et al.
Clinical Dysmorphology|October 10, 2020
Heterozygous intragenic deletions of FREM1 are not associated with trigonocephalyAngelika J Dawson, Karine Hovanes, Jing Liu, et al.
Pageof 2