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American Journal of Medical Genetics. Part A
|
September 12, 2012
Overgrowth with increased proliferation of fibroblast and matrix metalloproteinase activity related to reduced TIMP1: a newly recognized syndrome?
Brian Chung, Aleksander Hinek, Sarah Keating, et al.
Journal of Ultrasound in Medicine : Official Journal of the American Institute of Ultrasound in Medicine
|
May 6, 2024
Revisiting the Implications of a Wide or Narrow Fetal Cavum Septi Pellucidi
Joanna Sichitiu, Kimia Ghannad-Zadeh, Tim Van Mieghem, et al.
PEC Innovation
|
May 22, 2023
Development of a storytelling communication facilitation tool (SCFT) to facilitate discussion of complex genetic diagnoses between parents and their children: A pilot study using 22q11.2 deletion syndrome as a model condition
Simina Bogatan, Andrea Shugar, Syed Wasim, et al.
Journal of Clinical Medicine
|
October 6, 2018
Fetal Renal Echogenicity Associated with Maternal Focal Segmental Glomerulosclerosis: The Effect of Transplacental Transmission of Permeability Factor suPAR
Shirley Shuster, Ghada Ankawi, Christoph Licht, et al.
American Journal of Medical Genetics. Part A
|
December 31, 2003
Canavan disease: carrier-frequency determination in the Ashkenazi Jewish population and development of a novel molecular diagnostic assay
Annette Feigenbaum, Robert Moore, Joe Clarke, et al.
The American Journal of Psychiatry
|
January 5, 2002
Use of atypical antipsychotics during pregnancy and the risk of neural tube defects in infants
Gideon Koren, Tony Cohn, David Chitayat, et al.
AJNR. American Journal of Neuroradiology
|
January 21, 2026
Periventricular Nodular Heterotopia, Cerebellar Hypodysgenesis, and Mesial Temporal Malformation detected on Fetal MRI: An Under-Recognized Association
Vivek Pai, Shiri Shinar, Pradeep Krishnan, et al.
Prenatal Diagnosis
|
March 9, 2021
Prenatally diagnosed omphaloceles: Report of 92 cases and association with Beckwith-Wiedemann syndrome
Nimrah Abbasi, Aideen Moore, Priscilla Chiu, et al.
American Journal of Medical Genetics. Part A
|
November 15, 2007
Severe presentation of Beckwith-Wiedemann syndrome associated with high levels of constitutional paternal uniparental disomy for chromosome 11p15
Adam C Smith, Cheryl Shuman, David Chitayat, et al.
CJC Pediatric and Congenital Heart Disease
|
November 16, 2023
Exploring Barriers and Facilitators to Indirect Cascade Screening for Familial Hypercholesteraemia in a Paediatric/Parent Population
Megan A Dickson, Laura Zahavich, Janet Rush, et al.
Page
of 36
Search research articles
Search
Showing results (111-120 of 353) with videos related to
Sort By:
Page
of 36
American Journal of Medical Genetics. Part A
|
September 12, 2012
Overgrowth with increased proliferation of fibroblast and matrix metalloproteinase activity related to reduced TIMP1: a newly recognized syndrome?
Brian Chung, Aleksander Hinek, Sarah Keating, et al.
Journal of Ultrasound in Medicine : Official Journal of the American Institute of Ultrasound in Medicine
|
May 6, 2024
Revisiting the Implications of a Wide or Narrow Fetal Cavum Septi Pellucidi
Joanna Sichitiu, Kimia Ghannad-Zadeh, Tim Van Mieghem, et al.
PEC Innovation
|
May 22, 2023
Development of a storytelling communication facilitation tool (SCFT) to facilitate discussion of complex genetic diagnoses between parents and their children: A pilot study using 22q11.2 deletion syndrome as a model condition
Simina Bogatan, Andrea Shugar, Syed Wasim, et al.
Journal of Clinical Medicine
|
October 6, 2018
Fetal Renal Echogenicity Associated with Maternal Focal Segmental Glomerulosclerosis: The Effect of Transplacental Transmission of Permeability Factor suPAR
Shirley Shuster, Ghada Ankawi, Christoph Licht, et al.
American Journal of Medical Genetics. Part A
|
December 31, 2003
Canavan disease: carrier-frequency determination in the Ashkenazi Jewish population and development of a novel molecular diagnostic assay
Annette Feigenbaum, Robert Moore, Joe Clarke, et al.
The American Journal of Psychiatry
|
January 5, 2002
Use of atypical antipsychotics during pregnancy and the risk of neural tube defects in infants
Gideon Koren, Tony Cohn, David Chitayat, et al.
AJNR. American Journal of Neuroradiology
|
January 21, 2026
Periventricular Nodular Heterotopia, Cerebellar Hypodysgenesis, and Mesial Temporal Malformation detected on Fetal MRI: An Under-Recognized Association
Vivek Pai, Shiri Shinar, Pradeep Krishnan, et al.
Prenatal Diagnosis
|
March 9, 2021
Prenatally diagnosed omphaloceles: Report of 92 cases and association with Beckwith-Wiedemann syndrome
Nimrah Abbasi, Aideen Moore, Priscilla Chiu, et al.
American Journal of Medical Genetics. Part A
|
November 15, 2007
Severe presentation of Beckwith-Wiedemann syndrome associated with high levels of constitutional paternal uniparental disomy for chromosome 11p15
Adam C Smith, Cheryl Shuman, David Chitayat, et al.
CJC Pediatric and Congenital Heart Disease
|
November 16, 2023
Exploring Barriers and Facilitators to Indirect Cascade Screening for Familial Hypercholesteraemia in a Paediatric/Parent Population
Megan A Dickson, Laura Zahavich, Janet Rush, et al.
Page
of 36