Search research articles
Contact Us
Filters
Showing results (121-130 of 148) with videos related to
Page
of 15
Sort By:
European Journal of Human Genetics : EJHG
|
January 13, 2026
Childhood motor speech disorders: who to prioritise for genetic testing
Halianna Van Niel, Mariana Lauretta, Emma Baker, et al.
BMJ Open
|
January 14, 2025
Protocol for a multisite randomised controlled trial assessing the effect of the Telehealth for Early Developmental Intervention in babies born very preterm (TEDI-Prem) programme on neurodevelopmental outcomes and parent well-being
Abbey L Eeles, Alicia J Spittle, Stacey Dusing, et al.
BMC Pediatrics
|
April 25, 2014
Neurobehaviour between birth and 40 weeks' gestation in infants born <30 weeks' gestation and parental psychological wellbeing: predictors of brain development and child outcomes
Alicia J Spittle, Deanne K Thompson, Nisha C Brown, et al.
Molecular Psychiatry
|
February 22, 2018
A set of regulatory genes co-expressed in embryonic human brain is implicated in disrupted speech development
Else Eising, Amaia Carrion-Castillo, Arianna Vino, et al.
Journal of Medical Genetics
|
January 30, 2024
Expanding the phenotype of Kleefstra syndrome: speech, language and cognition in 103 individuals
Lottie D Morison, Milou G P Kennis, Dmitrijs Rots, et al.
Genetics in Medicine Open
|
December 13, 2024
GenIDA, a participatory patient registry for genetic forms of intellectual disability provides detailed caregiver-reported information on 237 individuals with Koolen-de Vries syndrome
Florent Colin, Pauline Burger, Timothée Mazzucotelli, et al.
European Journal of Human Genetics : EJHG
|
April 19, 2021
Clinical delineation of SETBP1 haploinsufficiency disorder
Nadieh A Jansen, Ruth O Braden, Siddharth Srivastava, et al.
Developmental Medicine and Child Neurology
|
March 21, 2022
Self-reported impact of developmental stuttering across the lifespan
Jessica O Boyce, Victoria E Jackson, Olivia van Reyk, et al.
Clinical Obesity
|
April 10, 2024
GNB1 and obesity: Evidence for a correlation between haploinsufficiency and syndromic obesity
Lotte Kleinendorst, Ozair Abawi, Niels Vos, et al.
Journal of Medical Genetics
|
November 3, 2022
In-depth characterisation of a cohort of individuals with missense and loss-of-function variants disrupting <i>FOXP2</i>
Lottie D Morison, Elisabeth Meffert, Miriam Stampfer, et al.
Page
of 15
Search research articles
Search
Showing results (121-130 of 148) with videos related to
Sort By:
Page
of 15
European Journal of Human Genetics : EJHG
|
January 13, 2026
Childhood motor speech disorders: who to prioritise for genetic testing
Halianna Van Niel, Mariana Lauretta, Emma Baker, et al.
BMJ Open
|
January 14, 2025
Protocol for a multisite randomised controlled trial assessing the effect of the Telehealth for Early Developmental Intervention in babies born very preterm (TEDI-Prem) programme on neurodevelopmental outcomes and parent well-being
Abbey L Eeles, Alicia J Spittle, Stacey Dusing, et al.
BMC Pediatrics
|
April 25, 2014
Neurobehaviour between birth and 40 weeks' gestation in infants born <30 weeks' gestation and parental psychological wellbeing: predictors of brain development and child outcomes
Alicia J Spittle, Deanne K Thompson, Nisha C Brown, et al.
Molecular Psychiatry
|
February 22, 2018
A set of regulatory genes co-expressed in embryonic human brain is implicated in disrupted speech development
Else Eising, Amaia Carrion-Castillo, Arianna Vino, et al.
Journal of Medical Genetics
|
January 30, 2024
Expanding the phenotype of Kleefstra syndrome: speech, language and cognition in 103 individuals
Lottie D Morison, Milou G P Kennis, Dmitrijs Rots, et al.
Genetics in Medicine Open
|
December 13, 2024
GenIDA, a participatory patient registry for genetic forms of intellectual disability provides detailed caregiver-reported information on 237 individuals with Koolen-de Vries syndrome
Florent Colin, Pauline Burger, Timothée Mazzucotelli, et al.
European Journal of Human Genetics : EJHG
|
April 19, 2021
Clinical delineation of SETBP1 haploinsufficiency disorder
Nadieh A Jansen, Ruth O Braden, Siddharth Srivastava, et al.
Developmental Medicine and Child Neurology
|
March 21, 2022
Self-reported impact of developmental stuttering across the lifespan
Jessica O Boyce, Victoria E Jackson, Olivia van Reyk, et al.
Clinical Obesity
|
April 10, 2024
GNB1 and obesity: Evidence for a correlation between haploinsufficiency and syndromic obesity
Lotte Kleinendorst, Ozair Abawi, Niels Vos, et al.
Journal of Medical Genetics
|
November 3, 2022
In-depth characterisation of a cohort of individuals with missense and loss-of-function variants disrupting <i>FOXP2</i>
Lottie D Morison, Elisabeth Meffert, Miriam Stampfer, et al.
Page
of 15