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Journal of Vascular Surgery Cases and Innovative Techniques
|
May 2, 2024
Spontaneous celiac artery aneurysms in 13-year-old and 10-year-old brothers with <i>PLOD1</i>-related kyphoscoliotic Ehlers-Danlos syndrome
Apoorva Bhandari, Victoria Siu, Audra A Duncan
Journal of Pediatric Genetics
|
February 10, 2017
Constitutional Epi/Genetic Conditions: Genetic, Epigenetic, and Environmental Factors
Laila C Schenkel, David Rodenhiser, Victoria Siu, et al.
European Journal of Medical Genetics
|
December 2, 2008
Unusual 8p inverted duplication deletion with telomere capture from 8q
Karen Buysse, Francesca Antonacci, Bert Callewaert, et al.
Journal of Otolaryngology - Head & Neck Surgery = Le Journal D'Oto-Rhino-Laryngologie Et De Chirurgie Cervico-Faciale
|
April 14, 2012
Neurofibromatosis and velopharyngeal insufficiency: is there an association?
Irene Zhang, Murad Husein, Anne Dworschak-Stokan, et al.
The Journal of Molecular Diagnostics : JMD
|
August 16, 2017
Clinical Validation of a Genome-Wide DNA Methylation Assay for Molecular Diagnosis of Imprinting Disorders
Erfan Aref-Eshghi, Laila C Schenkel, Hanxin Lin, et al.
American Journal of Medical Genetics. Part A
|
June 29, 2010
Facial diagnosis of mild and variant CdLS: Insights from a dysmorphologist survey
Sarika Rohatgi, Dinah Clark, Antonie D Kline, et al.
The Journal of Trauma and Acute Care Surgery
|
April 22, 2026
Quantifying costs during trauma bay resuscitation: A time-driven activity-based costing (TDABC) study
Mamadou Balde, Prakash Jayakumar, Victoria Siu, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques
|
March 7, 2018
Evidence for Cholinergic Dysfunction in Autosomal Dominant Kufs Disease
Pamela Jarrett, Alexander Easton, Kenneth Rockwood, et al.
American Journal of Medical Genetics. Part A
|
May 7, 2015
Deletion of 15q11.2(BP1-BP2) region: further evidence for lack of phenotypic specificity in a pediatric population
Bita Hashemi, Anne Bassett, David Chitayat, et al.
American Journal of Human Genetics
|
February 3, 2009
A multiplex human syndrome implicates a key role for intestinal cell kinase in development of central nervous, skeletal, and endocrine systems
Piya Lahiry, Jian Wang, John F Robinson, et al.
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Search research articles
Search
Showing results (1-10 of 20) with videos related to
Sort By:
Page
of 2
Journal of Vascular Surgery Cases and Innovative Techniques
|
May 2, 2024
Spontaneous celiac artery aneurysms in 13-year-old and 10-year-old brothers with <i>PLOD1</i>-related kyphoscoliotic Ehlers-Danlos syndrome
Apoorva Bhandari, Victoria Siu, Audra A Duncan
Journal of Pediatric Genetics
|
February 10, 2017
Constitutional Epi/Genetic Conditions: Genetic, Epigenetic, and Environmental Factors
Laila C Schenkel, David Rodenhiser, Victoria Siu, et al.
European Journal of Medical Genetics
|
December 2, 2008
Unusual 8p inverted duplication deletion with telomere capture from 8q
Karen Buysse, Francesca Antonacci, Bert Callewaert, et al.
Journal of Otolaryngology - Head & Neck Surgery = Le Journal D'Oto-Rhino-Laryngologie Et De Chirurgie Cervico-Faciale
|
April 14, 2012
Neurofibromatosis and velopharyngeal insufficiency: is there an association?
Irene Zhang, Murad Husein, Anne Dworschak-Stokan, et al.
The Journal of Molecular Diagnostics : JMD
|
August 16, 2017
Clinical Validation of a Genome-Wide DNA Methylation Assay for Molecular Diagnosis of Imprinting Disorders
Erfan Aref-Eshghi, Laila C Schenkel, Hanxin Lin, et al.
American Journal of Medical Genetics. Part A
|
June 29, 2010
Facial diagnosis of mild and variant CdLS: Insights from a dysmorphologist survey
Sarika Rohatgi, Dinah Clark, Antonie D Kline, et al.
The Journal of Trauma and Acute Care Surgery
|
April 22, 2026
Quantifying costs during trauma bay resuscitation: A time-driven activity-based costing (TDABC) study
Mamadou Balde, Prakash Jayakumar, Victoria Siu, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques
|
March 7, 2018
Evidence for Cholinergic Dysfunction in Autosomal Dominant Kufs Disease
Pamela Jarrett, Alexander Easton, Kenneth Rockwood, et al.
American Journal of Medical Genetics. Part A
|
May 7, 2015
Deletion of 15q11.2(BP1-BP2) region: further evidence for lack of phenotypic specificity in a pediatric population
Bita Hashemi, Anne Bassett, David Chitayat, et al.
American Journal of Human Genetics
|
February 3, 2009
A multiplex human syndrome implicates a key role for intestinal cell kinase in development of central nervous, skeletal, and endocrine systems
Piya Lahiry, Jian Wang, John F Robinson, et al.
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of 2