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American Journal of Medical Genetics. Part A
|
July 27, 2022
Speech and language development and genotype-phenotype correlation in 49 individuals with KAT6A syndrome
Miya St John, David J Amor, Angela T Morgan
The Medical Journal of Australia
|
October 8, 2009
Non-invasive prenatal diagnosis--toward a new horizon
Marleen R Susman, David J Amor, Jane L Halliday
Journal of Paediatrics and Child Health
|
December 31, 2013
Implementation of written consent for newborn screening in Victoria, Australia
Taryn Charles, James Pitt, Jane Halliday, et al.
Developmental Medicine and Child Neurology
|
August 8, 2018
Epigenetics of fragile X syndrome and fragile X-related disorders
Claudine M Kraan, David E Godler, David J Amor
American Journal of Medical Genetics. Part A
|
August 21, 2007
Two siblings with 46,XY DSD, congenital adrenal hypoplasia, aniridia, craniofacial, and skeletal abnormalities and intrauterine growth retardation: a new syndrome?
David J Coman, Susan M White, David J Amor
Developmental Medicine and Child Neurology
|
May 9, 2024
Statistical analysis of observational studies in disability research
Daisy A Shepherd, David J Amor, Margarita Moreno-Betancur
JAMA Network Open
|
July 20, 2021
Principles of Genomic Newborn Screening Programs: A Systematic Review
Lilian Downie, Jane Halliday, Sharon Lewis, et al.
American Journal of Medical Genetics. Part A
|
February 14, 2009
Pallister-Killian syndrome caused by mosaicism for a supernumerary ring chromosome 12p
Alison Yeung, David Francis, Olivia Giouzeppos, et al.
JAMA Neurology
|
June 10, 2014
Methylation analysis in newborn screening for fragile X syndrome
David E Godler, David J Amor, Howard R Slater
European Journal of Human Genetics : EJHG
|
November 17, 2016
Clinical utility gene card for: 16p12.2 microdeletion
Lucilla Pizzo, Joris Andrieux, David J Amor, et al.
Page
of 28
Search research articles
Search
Showing results (21-30 of 275) with videos related to
Sort By:
Page
of 28
American Journal of Medical Genetics. Part A
|
July 27, 2022
Speech and language development and genotype-phenotype correlation in 49 individuals with KAT6A syndrome
Miya St John, David J Amor, Angela T Morgan
The Medical Journal of Australia
|
October 8, 2009
Non-invasive prenatal diagnosis--toward a new horizon
Marleen R Susman, David J Amor, Jane L Halliday
Journal of Paediatrics and Child Health
|
December 31, 2013
Implementation of written consent for newborn screening in Victoria, Australia
Taryn Charles, James Pitt, Jane Halliday, et al.
Developmental Medicine and Child Neurology
|
August 8, 2018
Epigenetics of fragile X syndrome and fragile X-related disorders
Claudine M Kraan, David E Godler, David J Amor
American Journal of Medical Genetics. Part A
|
August 21, 2007
Two siblings with 46,XY DSD, congenital adrenal hypoplasia, aniridia, craniofacial, and skeletal abnormalities and intrauterine growth retardation: a new syndrome?
David J Coman, Susan M White, David J Amor
Developmental Medicine and Child Neurology
|
May 9, 2024
Statistical analysis of observational studies in disability research
Daisy A Shepherd, David J Amor, Margarita Moreno-Betancur
JAMA Network Open
|
July 20, 2021
Principles of Genomic Newborn Screening Programs: A Systematic Review
Lilian Downie, Jane Halliday, Sharon Lewis, et al.
American Journal of Medical Genetics. Part A
|
February 14, 2009
Pallister-Killian syndrome caused by mosaicism for a supernumerary ring chromosome 12p
Alison Yeung, David Francis, Olivia Giouzeppos, et al.
JAMA Neurology
|
June 10, 2014
Methylation analysis in newborn screening for fragile X syndrome
David E Godler, David J Amor, Howard R Slater
European Journal of Human Genetics : EJHG
|
November 17, 2016
Clinical utility gene card for: 16p12.2 microdeletion
Lucilla Pizzo, Joris Andrieux, David J Amor, et al.
Page
of 28