Whole genome sequencing identifies etiology of recurrent male intrauterine fetal death.

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Whole genome sequencing identifies etiology of recurrent male intrauterine fetal death.

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2017 nî lūn-bûn

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2017年学术文章

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Whole genome sequencing identifies etiology of recurrent male intrauterine fetal death.

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Whole genome sequencing identifies etiology of recurrent male intrauterine fetal death.

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Whole genome sequencing identifies etiology of recurrent male intrauterine fetal death.

@en

Whole genome sequencing identifies etiology of recurrent male intrauterine fetal death.

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Whole genome sequencing identifies etiology of recurrent male intrauterine fetal death.

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Whole genome sequencing identifies etiology of recurrent male intrauterine fetal death.

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P1476

Whole genome sequencing identifies etiology of recurrent male intrauterine fetal death

@en

P2093

David J Tester

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F Susan Cowchock

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Nicholas C Ackerman

http://www.w3.org/2001/XMLSchema#string

Omar Shehab

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A framework for variation discovery and genotyping using next-generation DNA sequencing data

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Fetal-onset IPEX: report of two families and review of literature.

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.

Causes of death among stillbirths.

Immunological analogy between allograft rejection, recurrent abortion and pre-eclampsia - the same basic mechanism?

P304

1040-1045

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scholarly article

P356

10.1002/PD.5142

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P433

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P478

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P50

Michael J Ackerman

P577

2017-09-12T00:00:00Z

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P698

28833278

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P921

stillbirth