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Clinical Ophthalmology (Auckland, N.Z.)
|
September 10, 2019
Brittle cornea syndrome: current perspectives
Andrew Walkden, Emma Burkitt-Wright, Leon Au
BMJ (Clinical Research Ed.)
|
April 1, 2004
Doctors' communication of trust, care, and respect in breast cancer: qualitative study
Emma Burkitt Wright, Christopher Holcombe, Peter Salmon
Clinical Dysmorphology
|
November 19, 2010
Cutaneous features in 17q21.31 deletion syndrome: a differential diagnosis for cardio-facio-cutaneous syndrome
Emma Burkitt Wright, Dian Donnai, Diana Johnson, et al.
Journal of Genetic Counseling
|
November 11, 2025
Healthcare professionals' perspectives on supporting individuals with NF1 during pregnancy and decision-making processes
Gamze Kaplan, Debbie M Smith, Ming Wai Wan, et al.
European Journal of Human Genetics : EJHG
|
April 22, 2026
Pregnancy experiences of expectant parents with Neurofibromatosis type 1: a qualitative interview study
Gamze Kaplan, Debbie M Smith, Ming Wai Wan, et al.
American Journal of Medical Genetics. Part A
|
June 7, 2017
A heterozygous microdeletion of 20p12.2-3 encompassing PROKR2 and BMP2 in a patient with congenital hypopituitarism and growth hormone deficiency
Samuel J H Parsons, Neville B Wright, Emma Burkitt-Wright, et al.
Developmental Medicine and Child Neurology
|
February 5, 2017
Autism spectrum disorder and other neurobehavioural comorbidities in rare disorders of the Ras/MAPK pathway
Shruti Garg, Ami Brooks, Amy Burns, et al.
Molecular Genetics and Metabolism
|
May 10, 2026
Natural history of hearing loss in adults with mucopolysaccharidoses across phenotype and genotype
Eamon P McCarron, Karolina M Stepien, Neil Summerfield, et al.
American Journal of Medical Genetics. Part A
|
January 7, 2026
Noonan Syndrome Spectrum Disorders Predispose to Systemic Lupus Erythematosus: Case Report and Critical Review of the Literature
Anastasia-Vasiliki Madenidou, Gillian I Rice, James O'Sullivan, et al.
Clinical Neurology and Neurosurgery
|
March 26, 2020
A retrospective regional study of aqueduct stenosis and fourth ventricle outflow obstruction in the paediatric complex neurofibromatosis type 1 population; Aetiology, clinical presentation and management
Christopher Murphy, Grace Vassallo, Emma Burkitt-Wright, et al.
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of 3
Search research articles
Search
Showing results (1-10 of 29) with videos related to
Sort By:
Page
of 3
Clinical Ophthalmology (Auckland, N.Z.)
|
September 10, 2019
Brittle cornea syndrome: current perspectives
Andrew Walkden, Emma Burkitt-Wright, Leon Au
BMJ (Clinical Research Ed.)
|
April 1, 2004
Doctors' communication of trust, care, and respect in breast cancer: qualitative study
Emma Burkitt Wright, Christopher Holcombe, Peter Salmon
Clinical Dysmorphology
|
November 19, 2010
Cutaneous features in 17q21.31 deletion syndrome: a differential diagnosis for cardio-facio-cutaneous syndrome
Emma Burkitt Wright, Dian Donnai, Diana Johnson, et al.
Journal of Genetic Counseling
|
November 11, 2025
Healthcare professionals' perspectives on supporting individuals with NF1 during pregnancy and decision-making processes
Gamze Kaplan, Debbie M Smith, Ming Wai Wan, et al.
European Journal of Human Genetics : EJHG
|
April 22, 2026
Pregnancy experiences of expectant parents with Neurofibromatosis type 1: a qualitative interview study
Gamze Kaplan, Debbie M Smith, Ming Wai Wan, et al.
American Journal of Medical Genetics. Part A
|
June 7, 2017
A heterozygous microdeletion of 20p12.2-3 encompassing PROKR2 and BMP2 in a patient with congenital hypopituitarism and growth hormone deficiency
Samuel J H Parsons, Neville B Wright, Emma Burkitt-Wright, et al.
Developmental Medicine and Child Neurology
|
February 5, 2017
Autism spectrum disorder and other neurobehavioural comorbidities in rare disorders of the Ras/MAPK pathway
Shruti Garg, Ami Brooks, Amy Burns, et al.
Molecular Genetics and Metabolism
|
May 10, 2026
Natural history of hearing loss in adults with mucopolysaccharidoses across phenotype and genotype
Eamon P McCarron, Karolina M Stepien, Neil Summerfield, et al.
American Journal of Medical Genetics. Part A
|
January 7, 2026
Noonan Syndrome Spectrum Disorders Predispose to Systemic Lupus Erythematosus: Case Report and Critical Review of the Literature
Anastasia-Vasiliki Madenidou, Gillian I Rice, James O'Sullivan, et al.
Clinical Neurology and Neurosurgery
|
March 26, 2020
A retrospective regional study of aqueduct stenosis and fourth ventricle outflow obstruction in the paediatric complex neurofibromatosis type 1 population; Aetiology, clinical presentation and management
Christopher Murphy, Grace Vassallo, Emma Burkitt-Wright, et al.
Page
of 3