Phenotypic definition of Chiari type I malformation coupled with high-density SNP genome screen shows significant evidence for linkage to regions on chromosomes 9 and 15.

Abee L Boyles; David S Enterline; Preston H Hammock; Deborah G Siegel; Susan H Slifer; Lorraine Mehltretter; John R Gilbert; Diane Hu-Lince; Dietrich Stephan; Ulrich Batzdorf

doi:10.1002/ajmg.a.31546

Phenotypic definition of Chiari type I malformation coupled with high-density SNP genome screen shows significant evidence for linkage to regions on chromosomes 9 and 15.

Identifier:nobleid.org/w1/20260515/7F673FEF

Type:Journal Article

0 views

Support unavailableClaim Your Authorship

View Original Paper Source

Embeddable Badge

[![NobleID](https://www.nobleid.org/api/badge/7F673FEF.svg?ark=w1%2F20260515%2F7F673FEF)](https://nobleid.org/work/w1/20260515/7F673FEF)

ARK Inflections

Metadata Policy

Metadata Formats

Bibliometric Analysis

Impact metrics, research fronts, co-authorship networks →

Authors & Claims

Paper Authors

Claim authorship of this work

Phenotypic definition of Chiari type I malformation coupled with high-density SNP genome screen shows significant evidence for linkage to regions on chromosomes 9 and 15.

Identifier:nobleid.org/w1/20260515/7F673FEF

Type:Journal Article

0 views

Support unavailableClaim Your Authorship

View Original Paper Source

Embeddable Badge

[![NobleID](https://www.nobleid.org/api/badge/7F673FEF.svg?ark=w1%2F20260515%2F7F673FEF)](https://nobleid.org/work/w1/20260515/7F673FEF)

ARK Inflections

Metadata Policy

Metadata Formats

Bibliometric Analysis

Impact metrics, research fronts, co-authorship networks →

Authors & Claims

Paper Authors

Claim authorship of this work