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Researchers at University of Jinan Report Findings in Meckel Syndrome (Whole exome sequencing identi...

Researchers at University of Jinan Report Findings in Meckel Syndrome (Whole exome sequencing identi...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_gale_infotracmisc_A609968330

Researchers at University of Jinan Report Findings in Meckel Syndrome (Whole exome sequencing identified a homozygous novel variant in CEP290 gene causes Meckel syndrome)

About this item

Full title

Researchers at University of Jinan Report Findings in Meckel Syndrome (Whole exome sequencing identified a homozygous novel variant in CEP290 gene causes Meckel syndrome)

Publisher

NewsRX LLC

Journal title

Health & Medicine Week, 2020, p.5765

Language

English

Publication information

Publisher

NewsRX LLC

More information

Alternative Titles

Full title

Researchers at University of Jinan Report Findings in Meckel Syndrome (Whole exome sequencing identified a homozygous novel variant in CEP290 gene causes Meckel syndrome)

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_gale_infotracmisc_A609968330

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_gale_infotracmisc_A609968330

Other Identifiers

ISSN

1531-6459

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