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 PMID:31259752  

Variable Features of Juvenile Polyposis Syndrome With Gastric Involvement Among Patients With a Large Genomic Deletion of BMPR1A.

Sari Lieberman | Rachel Beeri | Tom Walsh | Menachem Schechter | Dan Keret | Elizabet Half | Suleyman Gulsuner | Ariela Tomer | Harold Jacob | Shlomi Cohen | Lina Basel-Salmon | Mahmud Mansur | Rachel Berger | Lior H Katz | Eliahu Golomb | Tamar Peretz | Zohar Levy | Inbal Kedar | Mary-Claire King | Ephrat Levy-Lahad | Yael Goldberg
Clinical and translational gastroenterology | 2019

Loss-of-function mutations of BMPR1A cause juvenile polyposis syndrome (JPS), but large genomic deletions in BMPR1A are rare, reported in few families only, and data regarding the associated phenotype are limited.

Pubmed ID: 31259752

Research resources used in this publication

None found

Additional research tools detected in this publication

Antibodies used in this publication

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Associated grants

  • Agency: NCI NIH HHS, United States
    Id: R35 CA197458

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This is a list of tools and resources that we have found mentioned in this publication.


QIAGEN (tool)

RRID:SCR_008539

A commercial organization which provides assay technologies to isolate DNA, RNA, and proteins from any biological sample. Assay technologies are then used to make specific target biomolecules, such as the DNA of a specific virus, visible for subsequent analysis.

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Control-FREEC (tool)

RRID:SCR_010822

Prediction of copy number alterations and loss of heterozygosity using deep-sequencing data.

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