Exome and copy number variation analyses of Mayer-Rokitansky-Küster- Hauser syndrome

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Exome and copy number variation analyses of Mayer-Rokitansky-Küster- Hauser syndrome

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scientific article published on 27 September 2018

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wetenschappelijk artikel

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наукова стаття, опублікована у 2018

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Exome and copy number variation analyses of Mayer-Rokitansky-Küster- Hauser syndrome

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Exome and copy number variation analyses of Mayer-Rokitansky-Küster- Hauser syndrome

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Exome and copy number variation analyses of Mayer-Rokitansky-Küster- Hauser syndrome

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Exome and copy number variation analyses of Mayer-Rokitansky-Küster- Hauser syndrome

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Exome and copy number variation analyses of Mayer-Rokitansky-Küster- Hauser syndrome

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Exome and copy number variation analyses of Mayer-Rokitansky-Küster- Hauser syndrome

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P1476

Exome and copy number variation analyses of Mayer-Rokitansky-Küster- Hauser syndrome

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P2093

Hirofumi Kashiwagi

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Hirofumi Nakaoka

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Ituro Inoue

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Kazumi Takahashi

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Mari Shinoda

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Ryota Sugimoto

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Shingo Suzuki

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Shun-Ichiro Izumi

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Takahide Hayano

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Takahiro Suzuki

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P2860

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Clinical significance of high c-MYC and low MYCBP2 expression and their association with Ikaros dysfunction in adult acute lymphoblastic leukemia

iJGVD: an integrative Japanese genome variation database based on whole-genome sequencing.

Human genetic variation database, a reference database of genetic variations in the Japanese population.

Recurrent microdeletion at 17q12 as a cause of Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome: two case reports.

ParseCNV integrative copy number variation association software with quality tracking.

P2888

s41439-018-0028-4

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scholarly article

case report

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10.1038/S41439-018-0028-4

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English

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P478

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P50

Akane Kondo

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2018-09-27T00:00:00Z

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30302266

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P932

6160444

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