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

By:

Shen, Ming-Ching

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Producer: 20190404Description: 442-446 p. digitalISSN:

1521-0669

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Available from publisher's website

In: Pediatric hematology and oncology vol. 35

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Publication Type: Journal Article

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