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Population variation in total genetic risk of Hirschsprung disease from common RET, SEMA3 and NRG1 susceptibility polymorphisms. [electronic resource]

By:

Kapoor, Ashish

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Producer: 20160129Description: 2997-3003 p. digitalISSN:

1460-2083

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Available from publisher's website

In: Human molecular genetics vol. 24

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Publication Type: Journal Article; Research Support, N.I.H., Extramural

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