Increased prevalence of inherited neuromuscular disorders due to endogamy in Northeast Brazil: the need of community genetics services Silvana SantosAnne Aluska da Silva PequenoFernando Kok Original Article 26 November 2013 Pages: 199 - 203
Public attitudes regarding the use of electronic health information and residual clinical tissues for research Jeffrey R. BotkinErin RothwellJoyce Mitchell Original Article 05 December 2013 Pages: 205 - 213
“To perpetuate blindness!”: attitudes of UK patients with inherited retinal disease towards genetic testing Barbara PotrataMartin McKibbinJenny Hewison Original Article 24 December 2013 Pages: 215 - 222
Knowledge, attitudes, and barriers to carrier screening for the Ashkenazi Jewish panel: a Florida experience Jessica R. L. WarschSean WarschDeborah Barbouth Original Article 12 January 2014 Pages: 223 - 231
Family history of cancer associated with breast tumor clinicopathological features Luisel J. RicksAltovise EwingCarla Williams Original Article 15 January 2014 Pages: 233 - 240
Random inbreeding, isonymy, and population isolates in Argentina José DipierriAlvaro Rodríguez-LarraldeEmma Alfaro Original Article 06 February 2014 Pages: 241 - 248
The impact of participation in genetic research for families with cleft lip with and without cleft palate: a qualitative study Lynley J. DonoghueMargaret A. SahharLaura E. Forrest Original Article 06 February 2014 Pages: 249 - 256
Considerations for bio-specimen collection among black women residing in the rural Deep South participating in a cancer prevention study Tiffany L. CarsonClaudia M. HardyMonica L. Baskin Case Report 15 December 2013 Pages: 257 - 263
Carrier screening for inherited haemoglobin disorders among secondary school students and young adults in Latium, Italy Antonio AmatoMaria Pia CappabiancaRoberta Piscitelli Short Communication 27 October 2013 Pages: 265 - 268
Spatial and temporal analysis of infant mortality from congenital malformations in Brazil (1996–2010) Rubén BronbergLavinia Schuler-FacciniJosé Dipierri Country Report 01 October 2013 Pages: 269 - 282
Congenital and genetic disorders in the Sultanate of Oman. First attempt to assess healthcare needs A. RajabQ. Al SalmiM. A. Patton Country Report 02 March 2014 Pages: 283 - 289
