Paper Details

Paper Title

Universal newborn genetic screening for pediatric cancer predisposition syndromes: model-based insights.

Paper Journal Title

Genet Med

Paper Citation Count

Paper Publication Year

2021

Bio Mention

ALK, APC, CPS, CPS malignancy, DICER1, P, P/, P/LP, PHOX2B, PTCH1, RB1, RET, SMARCB1, SUFU, TP53, WT1, cancer, newborns, pediatric cancer, pediatric cancer predisposition syndromes, pediatric cancers

Mesh Descriptor

Author Name	Affiliation
Kurt D Christensen	Harvard Medical School
Kurt D Christensen	Harvard Pilgrim Health Care Institute
Robert C Green	Harvard Medical School
Robert C Green	Brigham and Women's Hospital and Broad Institute
Christine Y Lu	Harvard Medical School
Christine Y Lu	Harvard Pilgrim Health Care Institute
Heidi L Rehm	Harvard Medical School
Heidi L Rehm	Center for Genomic Medicine, Massachusetts General Hospital
Heidi L Rehm	Harvard Medical School
Heidi L Rehm	Center for Genomic Medicine, Massachusetts General Hospital
Marc S Williams	Genomic Medicine Institute
Ann Chen Wu	Harvard Medical School
Ann Chen Wu	Harvard Pilgrim Health Care Institute

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Dataset	Description	Source Link
ClinVar	ClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publ	Link
ClinVar	ClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.	Link
ClinVar	ClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publ	Link
ClinVar	ClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publ	Link
ClinVar	ClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.	Link
ClinVar	ClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publ	Link
ClinVar	ClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publ	Link
ClinVar	ClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publ	Link
ClinVar	ClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.	Link
ClinVar	ClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publ	Link
ClinVar	ClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.	Link
ClinVar	ClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.	Link
ClinVar	ClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.	Link
ClinVar	ClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.	Link
ClinVar	ClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publ	Link

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