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Paediatric & Neonatal Pain
|
July 7, 2025
Nationwide Cross-Sectional Online Survey of Australian Clinicians' Pain Management Practices for Newborns During Heel Lance Procedures
Sophie Jones, Nicole Pope, Margaret Broom, et al.
American Journal of Respiratory and Critical Care Medicine
|
January 13, 2022
Hereditary Mucin Deficiency Caused by Biallelic Loss of Function of <i>MUC5B</i>
Gregory Costain, Zhen Liu, Vito Mennella, et al.
Psychological Assessment
|
October 13, 2022
Measuring antenatal depressive symptoms across the world: A validation and cross-country invariance analysis of the Patient Health Questionnaire-9 (PHQ-9) in eight diverse low-resource settings
Aja Louise Murray, Chad Lance Hemady, Huyen Do, et al.
Annals of Neurology
|
September 17, 2014
Absent CNKSR2 causes seizures and intellectual, attention, and language deficits
Andrea K Vaags, Sarah Bowdin, Mary-Lou Smith, et al.
Journal of the Royal Society of New Zealand
|
October 23, 2024
Climate change adaptation through an integrative lens in Aotearoa New Zealand
Judy Lawrence, Anita Wreford, Paula Blackett, et al.
European Journal of Human Genetics : EJHG
|
February 18, 2018
Periodic reanalysis of whole-genome sequencing data enhances the diagnostic advantage over standard clinical genetic testing
Gregory Costain, Rebekah Jobling, Susan Walker, et al.
Archives of Women'S Mental Health
|
April 14, 2022
Perceived stress during the prenatal period: assessing measurement invariance of the Perceived Stress Scale (PSS-10) across cultures and birth parity
Laura Katus, Sarah Foley, Aja L Murray, et al.
Journal of Medical Genetics
|
October 26, 2010
Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disability
Alistair T Pagnamenta, Hameed Khan, Susan Walker, et al.
Cell Reports
|
November 10, 2016
DIXDC1 Phosphorylation and Control of Dendritic Morphology Are Impaired by Rare Genetic Variants
Vickie Kwan, Durga Praveen Meka, Sean H White, et al.
Human Mutation
|
April 14, 2025
A Palindrome-Like Structure on 16p13.3 Is Associated with the Formation of Complex Structural Variations and <i>SRRM2</i> Haploinsufficiency
Alistair T Pagnamenta, Jing Yu, Tracey A Willis, et al.
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of 26
Search research articles
Search
Showing results (191-200 of 260) with videos related to
Sort By:
Page
of 26
Paediatric & Neonatal Pain
|
July 7, 2025
Nationwide Cross-Sectional Online Survey of Australian Clinicians' Pain Management Practices for Newborns During Heel Lance Procedures
Sophie Jones, Nicole Pope, Margaret Broom, et al.
American Journal of Respiratory and Critical Care Medicine
|
January 13, 2022
Hereditary Mucin Deficiency Caused by Biallelic Loss of Function of <i>MUC5B</i>
Gregory Costain, Zhen Liu, Vito Mennella, et al.
Psychological Assessment
|
October 13, 2022
Measuring antenatal depressive symptoms across the world: A validation and cross-country invariance analysis of the Patient Health Questionnaire-9 (PHQ-9) in eight diverse low-resource settings
Aja Louise Murray, Chad Lance Hemady, Huyen Do, et al.
Annals of Neurology
|
September 17, 2014
Absent CNKSR2 causes seizures and intellectual, attention, and language deficits
Andrea K Vaags, Sarah Bowdin, Mary-Lou Smith, et al.
Journal of the Royal Society of New Zealand
|
October 23, 2024
Climate change adaptation through an integrative lens in Aotearoa New Zealand
Judy Lawrence, Anita Wreford, Paula Blackett, et al.
European Journal of Human Genetics : EJHG
|
February 18, 2018
Periodic reanalysis of whole-genome sequencing data enhances the diagnostic advantage over standard clinical genetic testing
Gregory Costain, Rebekah Jobling, Susan Walker, et al.
Archives of Women'S Mental Health
|
April 14, 2022
Perceived stress during the prenatal period: assessing measurement invariance of the Perceived Stress Scale (PSS-10) across cultures and birth parity
Laura Katus, Sarah Foley, Aja L Murray, et al.
Journal of Medical Genetics
|
October 26, 2010
Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disability
Alistair T Pagnamenta, Hameed Khan, Susan Walker, et al.
Cell Reports
|
November 10, 2016
DIXDC1 Phosphorylation and Control of Dendritic Morphology Are Impaired by Rare Genetic Variants
Vickie Kwan, Durga Praveen Meka, Sean H White, et al.
Human Mutation
|
April 14, 2025
A Palindrome-Like Structure on 16p13.3 Is Associated with the Formation of Complex Structural Variations and <i>SRRM2</i> Haploinsufficiency
Alistair T Pagnamenta, Jing Yu, Tracey A Willis, et al.
Page
of 26