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Search Results - Keigwin, Sylvia
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Multi‐exon COL5A1 deletion in a child with classical Ehlers–Danlos syndrome: A case report expanding the allelic spectrum and showing evidence of parental gonosomal mosaicism
by
Strang‐Karlsson, Sonja
,
Keigwin, Sylvia
,
Anttonen, Anna‐Kaisa
,
Baker, Duncan
,
Bean, Kerry
,
Jakkula, Eveliina
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Clinical case reports
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Diagnosis and management of vascular Ehlers-Danlos syndrome: Experience of the UK national diagnostic service, Sheffield
by
Bowen, Jessica M
,
Hernandez, Monica
,
Johnson, Diana S
,
Green, Claire
,
Kammin, Tammy
,
Baker, Duncan
,
Keigwin, Sylvia
,
Makino, Seiko
,
Taylor, Naomi
,
Watson, Oliver
,
Wheeldon, Nigel M
,
Sobey, Glenda J
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European journal of human genetics : EJHG
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