
THE GENETIC BACKGROUND OF SOUTHERN IRANIAN
COUPLES BEFORE MARRIAGE Nariman A, Sobhan MR, Savaei M, Aref-Eshghi E, Nourinejad R,
Manoochehri M, Ghahremani S, Daliri F, Daliri K,* *Corresponding Author: Dr. Karim Daliri, Department of Human Genetics, Behbahan Faculty of Medical Sciences, Bashir
Boulevard, Behbahan, Iran. Tel: +98-9374140937. Fax: +98-9374140937. E-mail: karimdaliri@ gmail.com page: 71
|
MATERIALS AND METHODS
Data Collection. The main proposal was approved
by the Research Ethics Committee of Behbahan School
of Paramedicine. All participants were assured that they
had the right to refuse to sign the consent form. For the
pilot study, 500 participants were selected from couples
who were referred to the Behbahan Marital Counseling
Center, located in Behbahan, a city in southern Iran, during
the period from January to November 2014, to obtain
information on consanguinity, disease history, and previous
referral to a medical genetics center.
The genetic counseling questionnaire included demographic
data (age, sex and ethnicity), and information
used to record different aspects of their medical history.
Regarding genetic counseling services, we asked participants:
“Have you ever been referred for genetic counseling
before?” For those who answered yes, we asked them to
provide the reason(s) for the referral(s) in a free-text item.
We also asked participants: “Have you ever been referred
for genetic testing, and if so, what were the results of the
tests?”
Other items evaluated their genetic background. One
item asked respondents to specify whether their marriage
was consanguineous (inbred) or non-consanguineous (outbred).
Couples who were consanguineous were asked to
indicate the degree of consanguinity. In a second item, the
participants were asked to report any genetic diseases in
their siblings or any experiences with infertility.
Data Analysis. Descriptive statistics and classical
tests of hypotheses were conducted using
STATA 11.0 software (http://en.softonic.com/s/
spss-11.0-free-full-version?ex-TOP-207.3).
|
|
|
|



 |
Number 27 VOL. 27 (2), 2024 |
Number 27 VOL. 27 (1), 2024 |
Number 26 Number 26 VOL. 26(2), 2023 All in one |
Number 26 VOL. 26(2), 2023 |
Number 26 VOL. 26, 2023 Supplement |
Number 26 VOL. 26(1), 2023 |
Number 25 VOL. 25(2), 2022 |
Number 25 VOL. 25 (1), 2022 |
Number 24 VOL. 24(2), 2021 |
Number 24 VOL. 24(1), 2021 |
Number 23 VOL. 23(2), 2020 |
Number 22 VOL. 22(2), 2019 |
Number 22 VOL. 22(1), 2019 |
Number 22 VOL. 22, 2019 Supplement |
Number 21 VOL. 21(2), 2018 |
Number 21 VOL. 21 (1), 2018 |
Number 21 VOL. 21, 2018 Supplement |
Number 20 VOL. 20 (2), 2017 |
Number 20 VOL. 20 (1), 2017 |
Number 19 VOL. 19 (2), 2016 |
Number 19 VOL. 19 (1), 2016 |
Number 18 VOL. 18 (2), 2015 |
Number 18 VOL. 18 (1), 2015 |
Number 17 VOL. 17 (2), 2014 |
Number 17 VOL. 17 (1), 2014 |
Number 16 VOL. 16 (2), 2013 |
Number 16 VOL. 16 (1), 2013 |
Number 15 VOL. 15 (2), 2012 |
Number 15 VOL. 15, 2012 Supplement |
Number 15 Vol. 15 (1), 2012 |
Number 14 14 - Vol. 14 (2), 2011 |
Number 14 The 9th Balkan Congress of Medical Genetics |
Number 14 14 - Vol. 14 (1), 2011 |
Number 13 Vol. 13 (2), 2010 |
Number 13 Vol.13 (1), 2010 |
Number 12 Vol.12 (2), 2009 |
Number 12 Vol.12 (1), 2009 |
Number 11 Vol.11 (2),2008 |
Number 11 Vol.11 (1),2008 |
Number 10 Vol.10 (2), 2007 |
Number 10 10 (1),2007 |
Number 9 1&2, 2006 |
Number 9 3&4, 2006 |
Number 8 1&2, 2005 |
Number 8 3&4, 2004 |
Number 7 1&2, 2004 |
Number 6 3&4, 2003 |
Number 6 1&2, 2003 |
Number 5 3&4, 2002 |
Number 5 1&2, 2002 |
Number 4 Vol.3 (4), 2000 |
Number 4 Vol.2 (4), 1999 |
Number 4 Vol.1 (4), 1998 |
Number 4 3&4, 2001 |
Number 4 1&2, 2001 |
Number 3 Vol.3 (3), 2000 |
Number 3 Vol.2 (3), 1999 |
Number 3 Vol.1 (3), 1998 |
Number 2 Vol.3(2), 2000 |
Number 2 Vol.1 (2), 1998 |
Number 2 Vol.2 (2), 1999 |
Number 1 Vol.3 (1), 2000 |
Number 1 Vol.2 (1), 1999 |
Number 1 Vol.1 (1), 1998 |
|
|