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Developmental Medicine and Child Neurology
|
December 19, 2023
Parents' preferences for receiving and discussing prognostic genetic information regarding their children's neurodevelopmental condition: A qualitative study
Erin Turbitt, Meg Bourne, Alison McEwen, et al.
American Journal of Obstetrics and Gynecology
|
August 12, 2023
The association between human chorionic gonadotropin and adverse pregnancy outcomes: a systematic review and meta-analysis
Monique Peris, Kylie Crompton, Daisy A Shepherd, et al.
Journal of Developmental and Behavioral Pediatrics : JDBP
|
January 17, 2025
Parents' Experiences and Views About Use of Wearable Technology for Research and Treatment Monitoring of Children with Neurodevelopmental Disorders
Rachel Xifaras, David J Amor, Erin Turbitt, et al.
Journal of Developmental and Behavioral Pediatrics : JDBP
|
February 17, 2025
Parents' Experiences and Views About Use of Wearable Technology for Research and Treatment Monitoring of Children with Neurodevelopmental Disorders
Rachel Xifaras, David J Amor, Erin Turbitt, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
March 18, 2008
Increased genetic counseling support improves communication of genetic information in families
Laura E Forrest, Jo Burke, Sonya Bacic, et al.
Journal of Paediatrics and Child Health
|
January 17, 2013
Considerations for reporting genome results to patients
Erin Turbitt, David J Amor, Jane L Halliday, et al.
Disability and Health Journal
|
October 15, 2024
Parents' perspectives on conversations about prognosis and an assessment of prognostic information available online: A mixed-methods study
Akira Gokoolparsadh, Meg Bourne, Alison McEwen, et al.
American Journal of Medical Genetics. Part A
|
June 29, 2021
Personal utility of genomic sequencing for infants with congenital deafness
Erin Tutty, David J Amor, Anna Jarmolowicz, et al.
American Journal of Medical Genetics. Part A
|
August 30, 2007
Keipert syndrome (Nasodigitoacoustic syndrome) is X-linked and maps to Xq22.2-Xq28
David J Amor, Hans-Henrik M Dahl, Melanie Bahlo, et al.
Stem Cell Research
|
February 8, 2026
Generation of two tetracycline-inducible NGN2 iN iPSC lines carrying a heterozygous floating-Harbor syndrome SRCAP truncating mutation
Inbal Kantor, Jordan L Wright, David J Amor, et al.
Page
of 28
Search research articles
Search
Showing results (31-40 of 275) with videos related to
Sort By:
Page
of 28
Developmental Medicine and Child Neurology
|
December 19, 2023
Parents' preferences for receiving and discussing prognostic genetic information regarding their children's neurodevelopmental condition: A qualitative study
Erin Turbitt, Meg Bourne, Alison McEwen, et al.
American Journal of Obstetrics and Gynecology
|
August 12, 2023
The association between human chorionic gonadotropin and adverse pregnancy outcomes: a systematic review and meta-analysis
Monique Peris, Kylie Crompton, Daisy A Shepherd, et al.
Journal of Developmental and Behavioral Pediatrics : JDBP
|
January 17, 2025
Parents' Experiences and Views About Use of Wearable Technology for Research and Treatment Monitoring of Children with Neurodevelopmental Disorders
Rachel Xifaras, David J Amor, Erin Turbitt, et al.
Journal of Developmental and Behavioral Pediatrics : JDBP
|
February 17, 2025
Parents' Experiences and Views About Use of Wearable Technology for Research and Treatment Monitoring of Children with Neurodevelopmental Disorders
Rachel Xifaras, David J Amor, Erin Turbitt, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
March 18, 2008
Increased genetic counseling support improves communication of genetic information in families
Laura E Forrest, Jo Burke, Sonya Bacic, et al.
Journal of Paediatrics and Child Health
|
January 17, 2013
Considerations for reporting genome results to patients
Erin Turbitt, David J Amor, Jane L Halliday, et al.
Disability and Health Journal
|
October 15, 2024
Parents' perspectives on conversations about prognosis and an assessment of prognostic information available online: A mixed-methods study
Akira Gokoolparsadh, Meg Bourne, Alison McEwen, et al.
American Journal of Medical Genetics. Part A
|
June 29, 2021
Personal utility of genomic sequencing for infants with congenital deafness
Erin Tutty, David J Amor, Anna Jarmolowicz, et al.
American Journal of Medical Genetics. Part A
|
August 30, 2007
Keipert syndrome (Nasodigitoacoustic syndrome) is X-linked and maps to Xq22.2-Xq28
David J Amor, Hans-Henrik M Dahl, Melanie Bahlo, et al.
Stem Cell Research
|
February 8, 2026
Generation of two tetracycline-inducible NGN2 iN iPSC lines carrying a heterozygous floating-Harbor syndrome SRCAP truncating mutation
Inbal Kantor, Jordan L Wright, David J Amor, et al.
Page
of 28