Volume 16; Issue 4

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Genetics in Medicine
Volume 16; Issue 4

Genetics in Medicine

Volume 16; Issue 4

1

Familial incidence and associated symptoms in a population of individuals with nonsyndromic craniosynostosis

Greenwood, Jaclyn, Flodman, Pamela, Osann, Kathryn, Boyadjiev, Simeon A., Kimonis, Virginia

Journal:

Genetics in Medicine

Year:

2014

Language:

english

File:

PDF, 332 KB

english, 2014

2

Processes and factors involved in decisions regarding return of incidental genomic findings in research

Klitzman, Robert, Buquez, Brigitte, Appelbaum, Paul S., Fyer, Abby, Chung, Wendy K.

Journal:

Genetics in Medicine

Year:

2014

Language:

english

File:

PDF, 348 KB

english, 2014

3

Recommendations from the EGAPP Working Group: does PCA3 testing for the diagnosis and management of prostate cancer improve patient health outcomes?

Journal:

Genetics in Medicine

Year:

2014

Language:

english

File:

PDF, 377 KB

english, 2014

4

Communication of genetic test results to family and health-care providers following disclosure of research results

Graves, Kristi D., Sinicrope, Pamela S., Esplen, Mary Jane, Peterson, Susan K., Patten, Christi A., Lowery, Jan, Sinicrope, Frank A., Nigon, Sandra K., Borgen, Joyce, Sheinfeld Gorin, Sherri, Keogh, L

Journal:

Genetics in Medicine

Year:

2014

Language:

english

File:

PDF, 421 KB

english, 2014

5

Noninvasive prenatal testing: limitations and unanswered questions

Lutgendorf, Monica A., Stoll, Katie A., Knutzen, Dana M., Foglia, Lisa M.

Journal:

Genetics in Medicine

Year:

2014

Language:

english

File:

PDF, 280 KB

english, 2014

6

Determining pathogenicity of genetic variants in hypertrophic cardiomyopathy: importance of periodic reassessment

Das K, Jipin, Ingles, Jodie, Bagnall, Richard D., Semsarian, Christopher

Journal:

Genetics in Medicine

Year:

2014

Language:

english

File:

PDF, 437 KB

english, 2014

7

In This Issue

Journal:

Genetics in Medicine

Year:

2014

Language:

english

File:

PDF, 314 KB

english, 2014

8

22q13.2q13.32 genomic regions associated with severity of speech delay, developmental delay, and physical features in Phelan–McDermid syndrome

Sarasua, Sara M., Dwivedi, Alka, Boccuto, Luigi, Chen, Chin-Fu, Sharp, Julia L., Rollins, Jonathan D., Collins, Julianne S., Rogers, R. Curtis, Phelan, Katy, DuPont, Barbara R.

Journal:

Genetics in Medicine

Year:

2014

Language:

english

File:

PDF, 905 KB

english, 2014

9

News Briefs

Journal:

Genetics in Medicine

Year:

2014

Language:

english

File:

PDF, 203 KB

english, 2014

10

Factors affecting maternal participation in the genetic component of the National Birth Defects Prevention Study—United States, 1997–2007

Glidewell, Jill, Reefhuis, Jennita, Rasmussen, Sonja A., Woomert, Alison, Hobbs, Charlotte, Romitti, Paul A., Crider, Krista S.

Journal:

Genetics in Medicine

Year:

2014

Language:

english

File:

PDF, 378 KB

english, 2014

11

American College of Medical Genetics and Genomics guideline for the clinical evaluation and etiologic diagnosis of hearing loss

Alford, Raye L., Arnos, Kathleen S., Fox, Michelle, Lin, Jerry W., Palmer, Christina G., Pandya, Arti, Rehm, Heidi L., Robin, Nathaniel H., Scott, Daryl A., Yoshinaga-Itano, Christine

Journal:

Genetics in Medicine

Year:

2014

Language:

english

File:

PDF, 534 KB

english, 2014

12

Corrigendum: Phenylalanine hydroxylase deficiency: diagnosis and management guideline

Journal:

Genetics in Medicine

Year:

2014

File:

PDF, 246 KB

2014