Novel hereditary spherocytosis-associated splice site mutation in the ANK1 gene caused by parental gonosomal mosaicism.

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Novel hereditary spherocytosis-associated splice site mutation in the ANK1 gene caused by parental gonosomal mosaicism.

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2018 nî lūn-bûn

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2018年の論文

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年學術文章

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Novel hereditary spherocytosis ...... parental gonosomal mosaicism.

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Novel hereditary spherocytosis ...... parental gonosomal mosaicism.

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Novel hereditary spherocytosis ...... parental gonosomal mosaicism.

@en

Novel hereditary spherocytosis ...... parental gonosomal mosaicism.

@nl

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Novel hereditary spherocytosis ...... parental gonosomal mosaicism.

@en

Novel hereditary spherocytosis ...... parental gonosomal mosaicism.

@nl

P1476

Novel hereditary spherocytosis ...... parental gonosomal mosaicism.

@en

P2093

Ming Huang

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Na Shen

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Qun Hu

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Xiong Wang

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Yanjun Lu

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P2860

Structural basis for spectrin recognition by ankyrin

Structure of the ZU5-ZU5-UPA-DD tandem of ankyrin-B reveals interaction surfaces necessary for ankyrin function

Parental somatic mosaicism is underrecognized and influences recurrence risk of genomic disorders

SWISS-MODEL: modelling protein tertiary and quaternary structure using evolutionary information

A genomic view of mosaicism and human disease.

A systematic review of hereditary spherocytosis reported in Chinese biomedical journals from 1978 to 2013 and estimation of the prevalence of the disease using a disease model.

Timing, rates and spectra of human germline mutation.

Hereditary spherocytosis, elliptocytosis, and other red cell membrane disorders.

Improving the limit of detection for Sanger sequencing: A comparison of methodologies for KRAS variant detection.

Recommendations regarding splenectomy in hereditary hemolytic anemias.

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e219-e222

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P31

scholarly article

P356

10.3324/HAEMATOL.2017.186551

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P433

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P478

103

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P577

2018-02-15T00:00:00Z

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29449435

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P932

5927983

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