Cite

Zorrilla M, Yatsenko AN. The genetics of infertility: Current status of the field. Curr Genet Med Rep. 2013; 1(4): 247-260.ZorrillaMYatsenkoAN.The genetics of infertility: Current status of the fieldCurr Genet Med Rep20131424726010.1007/s40142-013-0027-1388517424416713Search in Google Scholar

Bittles AH, Black ML. Evolution in health and medicine Sackler colloquium: Consanguinity, human evolution, and complex diseases. Proc Natl Acad Sci USA. 2010; 107(Suppl 1): 1779-1786.BittlesAHBlackML.Evolution in health and medicine Sackler colloquium: Consanguinity, human evolution, and complex diseasesProc Natl Acad Sci USA2010107Suppl 11779178610.1073/pnas.0906079106286828719805052Search in Google Scholar

Tadmouri GO, Nair P, Obeid T, Al Ali MT, Al Khaja N, Hamamy HA. Consanguinity and reproductive health among Arabs. Reprod Health. 2009; 6:17. doi: 10.1186/1742- 4755-6-17.TadmouriGONairPObeidTAl AliMTAl KhajaNHamamyHAConsanguinity and reproductive health among ArabsReprod Health2009617doi: 10.1186/1742- 4755-6-17Open DOISearch in Google Scholar

Saadat M, Ansari-Lari M, Farhud DD. Consanguineous marriage in Iran. Ann Hum Biol. 2004; 31(2): 263-269.SaadatMAnsari-LariMFarhudDD.Consanguineous marriage in IranAnn Hum Biol200431226326910.1080/0301446031000165221115204368Search in Google Scholar

Aref Eshghi E, Masoumi P. Genetic and demographic analysis of retinitis pigmentosa in Iran during 2007-2008. Med Sci J Islamic Azad Univ Tehran Med Branch. 2012; 22(1): 78-84. (www.iau-tmuj.ir/browse. php?a_id=545&sid=1&slc.lang-en)Aref EshghiEMasoumiP.Genetic and demographic analysis of retinitis pigmentosa in Iran during 2007-2008Med Sci J Islamic Azad Univ Tehran Med Branch20122217884www.iau-tmuj.ir/browse. php?a_id=545&sid=1&slc.lang-enSearch in Google Scholar

Rull K, Nagirnaja L, Laan M. Genetics of recurrent miscarriage: Challenges, current knowledge, future directions. Front Genet. 2012; 3: 34. doi: 10.3389/fgene.2012. 00034.RullKNagirnajaLLaanM.Genetics of recurrent miscarriage: Challenges, current knowledge, future directionsFront Genet2012334doi: 10.3389/fgene.2012. 00034Open DOISearch in Google Scholar

Helm BM. Exploring the genetic counselor’s role in facilitating meaning-making: Rare disease diagnoses. J Genet Couns. 2015; 24(2): 205-212.HelmBM.Exploring the genetic counselor’s role in facilitating meaning-making: Rare disease diagnosesJ Genet Couns201524220521210.1007/s10897-014-9812-625566742Search in Google Scholar

Lee H, Deignan JL, Dorrani N, Strom SP, Kantarci S, Quintero-Rivera F, et al. Clinical exome sequencing for genetic identification of rare Mendelian disorders. JAMA 2014; 312(18): 1880-1887.LeeHDeignanJLDorraniNStromSPKantarciSQuintero-RiveraF,et alClinical exome sequencing for genetic identification of rare Mendelian disordersJAMA2014312181880188710.1001/jama.2014.14604427863625326637Search in Google Scholar

Zlotogora J. Population programs for the detection of couples at risk for severe monogenic genetic diseases. Hum Genet. 2009; 126(2): 247-253.ZlotogoraJ.Population programs for the detection of couples at risk for severe monogenic genetic diseasesHum Genet2009126224725310.1007/s00439-009-0669-y19390864Search in Google Scholar

Boland PM, Ruth K, Matro JM, Rainey KL, Fang CY, Wong YN, et al. Genetic counselors’ (GC) knowledge, awareness, understanding of clinical next-generation sequencing (NGS) genomic testing. Clin Genet. 2014; 88(6): 565-572.BolandPMRuthKMatroJMRaineyKLFangCYWongYN,et alGenetic counselors’ (GC) knowledge, awareness, understanding of clinical next-generation sequencing (NGS) genomic testingClin Genet201488656557210.1111/cge.12555447477425523111Search in Google Scholar

Fathzadeh M, Bigi MA, Bazrgar M, Yavarian M, Tabatabaee HR, Akrami SM. Genetic counseling in southern Iran: Consanguinity and reason for referral. J Genet Couns. 2008; 17(5): 472-479.FathzadehMBigiMABazrgarMYavarianMTabatabaeeHRAkramiSM.Genetic counseling in southern Iran: Consanguinity and reason for referralJ Genet Couns200817547247910.1007/s10897-008-9163-218551360Search in Google Scholar

Ormond KE. From genetic counseling to “genomic counseling.” Mol Genet Genomic Med. 2013; 1(4): 189-193.OrmondKE.From genetic counseling to “genomic counseling.”Mol Genet Genomic Med20131418919310.1002/mgg3.45386558724498615Search in Google Scholar

eISSN:
1311-0160
Language:
English
Publication timeframe:
2 times per year
Journal Subjects:
Medicine, Basic Medical Science, other