Volume 17 Issue 3, March 2015

News Briefs

Primary-care providers’ perceived barriers to integration of genetics services: a systematic review of the literature

• Natalie A. Mikat-Stevens
• Ingrid A. Larson
• Beth A. Tarini

Increased frequency of FBN1 truncating and splicing variants in Marfan syndrome patients with aortic events

• Linnea M. Baudhuin
• Katrina E. Kotzer
• Susan A. Lagerstedt

Exceptional aggressiveness of cerebral cavernous malformation disease associated with PDCD10 mutations

• Robert Shenkar
• Changbin Shi
• Issam A. Awad

The impact of reporting incidental findings from exome and whole-genome sequencing: predicted frequencies based on modeling

• Lucy-Enid Ding
• Leslie Burnett
• Douglas Chesher

Outcomes of individuals with profound and partial biotinidase deficiency ascertained by newborn screening in Michigan over 25 years

• Allison M. Jay
• Robert L. Conway
• Barry Wolf

Identification of OSBPL2 as a novel candidate gene for progressive nonsyndromic hearing loss by whole-exome sequencing

• Guangqian Xing
• Jun Yao
• Xin Cao

Molecular genetic testing for cystic fibrosis: laboratory performance on the College of American Pathologists external proficiency surveys

• Elaine Lyon
• Iris Schrijver
• Glenn E. Palomaki

Informed consent for biobanking: consensus-based guidelines for adequate comprehension

• Laura M. Beskow
• Carrie B. Dombeck
• Kevin P. Weinfurt

Discordant noninvasive prenatal testing and cytogenetic results: a study of 109 consecutive cases

• Jia-Chi Wang
• Trilochan Sahoo
• Charles M. Strom

Adverse events in cancer patients with sickle cell trait or disease: case reports

• Helen Swede
• Biree Andemariam
• Richard G. Stevens

Erratum: In This Issue

ADDENDUM: Reviewer Acknowledgment 2014