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Pediatric Hematology and Oncology Volume 35, 2018 - Issue 7-8
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Letter

Segmental uniparental disomy as a rare cause of congenital severe factor XIII deficiency in a girl with only one heterozygous carrier parent

Ming-Ching ShenDepartment of Laboratory Medicine, National Taiwan University Hospital, Taipei, Taiwan; ;Department of Internal Medicine, Changhua Christian Hospital, Changhua, Taiwan; ;Department of Laboratory Medicine, Changhua Christian Hospital, Changhua, Taiwan; Correspondence[email protected]
ORCID Iconhttp://orcid.org/0000-0001-7789-2148
ORCID Icon,
Ming ChenDepartment of Genomic Medicine, Changhua Christian Hospital, Changhua, Taiwan;
,
Shung-Ping ChangDepartment of Genomic Medicine, Changhua Christian Hospital, Changhua, Taiwan;
,
Po-Te LinDepartment of Internal Medicine, Changhua Christian Hospital, Changhua, Taiwan;
,
Han-Ni HsiehDepartment of Internal Medicine, Changhua Christian Hospital, Changhua, Taiwan;
&
Kai-Hsin LinDepartment of Pediatrics, National Taiwan University Hospital, Taipei, Taiwan
Pages 442-446 | Received 24 Jul 2018, Accepted 06 Nov 2018, Published online: 31 Jan 2019

References

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  • The Human Gene Mutation Database, at the Institute of Medical Genetics in Cardiff NM000129.3, http://www.hgmd.cf.ac.uk/ac/gene.php?gene=F13A1. Accessed February 2018.
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