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Pediatric Dermatology
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April 28, 2007
Mosaic chromosome 6 trisomy in an epidermal nevus
Glenda J Sobey, Oliver W Quarrell, Steven Williams, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
|
February 14, 2017
Ehlers-Danlos syndrome, classical type
Jessica M Bowen, Glenda J Sobey, Nigel P Burrows, et al.
Clinical Dysmorphology
|
December 2, 2014
Ultrastructural and histological findings on examination of skin in osteogenesis imperfecta: a novel study
Meena Balasubramanian, Bart E Wagner, Luiz C Peres, et al.
European Journal of Human Genetics : EJHG
|
March 28, 2023
Diagnosis and management of vascular Ehlers-Danlos syndrome: Experience of the UK national diagnostic service, Sheffield
Jessica M Bowen, Monica Hernandez, Diana S Johnson, et al.
American Journal of Medical Genetics. Part A
|
September 1, 2016
Phenotypic variability in patients with osteogenesis imperfecta caused by BMP1 mutations
Rebecca C Pollitt, Vrinda Saraff, Ann Dalton, et al.
European Journal of Human Genetics : EJHG
|
April 17, 2025
Vascular Ehlers Danlos Syndrome and Chromosome 2q32 Microdeletion Syndrome
Claire E Green, Shadi Albaba, Glenda J Sobey, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
|
March 18, 2017
The 2017 international classification of the Ehlers-Danlos syndromes
Fransiska Malfait, Clair Francomano, Peter Byers, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 7) with videos related to
Sort By:
Page
of 1
Pediatric Dermatology
|
April 28, 2007
Mosaic chromosome 6 trisomy in an epidermal nevus
Glenda J Sobey, Oliver W Quarrell, Steven Williams, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
|
February 14, 2017
Ehlers-Danlos syndrome, classical type
Jessica M Bowen, Glenda J Sobey, Nigel P Burrows, et al.
Clinical Dysmorphology
|
December 2, 2014
Ultrastructural and histological findings on examination of skin in osteogenesis imperfecta: a novel study
Meena Balasubramanian, Bart E Wagner, Luiz C Peres, et al.
European Journal of Human Genetics : EJHG
|
March 28, 2023
Diagnosis and management of vascular Ehlers-Danlos syndrome: Experience of the UK national diagnostic service, Sheffield
Jessica M Bowen, Monica Hernandez, Diana S Johnson, et al.
American Journal of Medical Genetics. Part A
|
September 1, 2016
Phenotypic variability in patients with osteogenesis imperfecta caused by BMP1 mutations
Rebecca C Pollitt, Vrinda Saraff, Ann Dalton, et al.
European Journal of Human Genetics : EJHG
|
April 17, 2025
Vascular Ehlers Danlos Syndrome and Chromosome 2q32 Microdeletion Syndrome
Claire E Green, Shadi Albaba, Glenda J Sobey, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
|
March 18, 2017
The 2017 international classification of the Ehlers-Danlos syndromes
Fransiska Malfait, Clair Francomano, Peter Byers, et al.
Page
of 1