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Gareth Baynam

Showing results (1-10 of 178) with videos related to

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Journal of Law and Medicine|May 15, 2020
Consideration of a Legislative Framework to Support the Diagnostic Odyssey Commonly Encountered in the Instance of Rare DiseaseMarisa Taliangis, Gareth Baynam
Frontiers in Public Health|June 28, 2019
Editorial: Public Health GenomicsPaul Lacaze, Gareth Baynam
Advances in Experimental Medicine and Biology|August 7, 2010
Cornelia de Lange syndromeJinglan Liu, Gareth Baynam
Journal of Maxillofacial and Oral Surgery|November 10, 2012
45,X/46,XY mosaicism and Oculo-Auriculo-Vertebral Spectrum following an IVF pregnancy: a report and a discussion of their interrelationshipsGareth Baynam, Jack Goldblatt
JAMA Pediatrics|June 7, 2017
New Opportunities for Evidence in Fetal Alcohol Spectrum DisorderCarol Bower, Gareth Baynam
The Lancet. Global Health|June 1, 2024
Erasing stigma around rare diseasesDavid A Pearce, Gareth Baynam
American Journal of Medical Genetics. Part A|May 13, 2008
Deletion of 8p23.1 with features of Cornelia de Lange syndrome and congenital diaphragmatic hernia and a review of deletions of 8p23.1 to 8pter? A further locus for Cornelia de Lange syndromeGareth Baynam, Jack Goldblatt, Ian Walpole
Clinical Dysmorphology|June 9, 2006
A case of 3q29 microdeletion with novel features and a review of cytogenetically visible terminal 3q deletionsGareth Baynam, Jack Goldblatt, Sharron Townshend
American Journal of Medical Genetics. Part A|August 2, 2008
A c.1019A > G mutation in FGFR2, which predicts p.Tyr340Cys, in a lethally malformed fetus with Pfeiffer syndrome and multiple pterygiaGareth Baynam, Nicholas Smith, Jack Goldblatt
BMJ Case Reports|June 9, 2012
A child with an STK11 mutation and Sotos syndrome-like features: can STK11 mutations produce a Sotos syndrome phenocopy?Gareth Baynam, Lyn Schofield, Jack Goldblatt
Pageof 18

Showing results (1-10 of 178) with videos related to

Sort By:
Pageof 18
Journal of Law and Medicine|May 15, 2020
Consideration of a Legislative Framework to Support the Diagnostic Odyssey Commonly Encountered in the Instance of Rare DiseaseMarisa Taliangis, Gareth Baynam
Frontiers in Public Health|June 28, 2019
Editorial: Public Health GenomicsPaul Lacaze, Gareth Baynam
Advances in Experimental Medicine and Biology|August 7, 2010
Cornelia de Lange syndromeJinglan Liu, Gareth Baynam
Journal of Maxillofacial and Oral Surgery|November 10, 2012
45,X/46,XY mosaicism and Oculo-Auriculo-Vertebral Spectrum following an IVF pregnancy: a report and a discussion of their interrelationshipsGareth Baynam, Jack Goldblatt
JAMA Pediatrics|June 7, 2017
New Opportunities for Evidence in Fetal Alcohol Spectrum DisorderCarol Bower, Gareth Baynam
The Lancet. Global Health|June 1, 2024
Erasing stigma around rare diseasesDavid A Pearce, Gareth Baynam
American Journal of Medical Genetics. Part A|May 13, 2008
Deletion of 8p23.1 with features of Cornelia de Lange syndrome and congenital diaphragmatic hernia and a review of deletions of 8p23.1 to 8pter? A further locus for Cornelia de Lange syndromeGareth Baynam, Jack Goldblatt, Ian Walpole
Clinical Dysmorphology|June 9, 2006
A case of 3q29 microdeletion with novel features and a review of cytogenetically visible terminal 3q deletionsGareth Baynam, Jack Goldblatt, Sharron Townshend
American Journal of Medical Genetics. Part A|August 2, 2008
A c.1019A > G mutation in FGFR2, which predicts p.Tyr340Cys, in a lethally malformed fetus with Pfeiffer syndrome and multiple pterygiaGareth Baynam, Nicholas Smith, Jack Goldblatt
BMJ Case Reports|June 9, 2012
A child with an STK11 mutation and Sotos syndrome-like features: can STK11 mutations produce a Sotos syndrome phenocopy?Gareth Baynam, Lyn Schofield, Jack Goldblatt
Pageof 18