A modified program designed to screen for the Tay-Sachs carrier is presented in which testing is limited to one or both partners, as needed, in an Ashkenazi Jewish (Jews of central and eastern Europeancestry) mating when there is a definite commitment toward having a child, or in the early stages of the pregnancy. Testing of unmarried indi-viduals is discouraged. The approach maximizes individ-ualization of both the medical and laboratory aspects of the program and promotes a positive and beneficial rela-tionship between physician and clinical chemist. There is little involvement of the lay population or clergy, and no special sources of funding are required. Whereas most mass screening programs for the Tay-Sachs carrier have attempted to e...
The primary goal of carrier screening is to identify asymptomatic individuals who carry variants ass...
Introduction: Tay Sachs Disease (TSD) is a fatal genetic disorder with autosomal recessive inheritan...
CONTEXT: Tay-Sachs disease is an autosomal recessive disease characterized by progressive neurologic...
Tay-Sachs disease is a fatal genetic disease affecting Jewish infants of eastern European ancestry. ...
Objective: To give recommendations to physicians and midwives providing pre-conception or prenatal c...
C1 - Journal Articles RefereedA screening programme for Tay Sachs disease (TSD) carrier status was i...
Carrier screening for autosomal recessive disorders aims to facilitate reproductive decision-making ...
Tay-Sachs disease (TSD) is a fatal, recessively inherited neurodegenerative condition of infancy and...
Reproductive carrier screening started in some countries in the 1970s for hemoglobinopathies and Tay...
In Yemen, the prevalence of sickle cell trait and b-thalassemia trait are high. The aim of this prem...
Background: Carrier screening for autosomal recessive disorders aims to facilitate reproductive deci...
One of the primary aims of the genetic counselor is the reduction in the number of children born wit...
Background: Carrier screening for autosomal recessive disorders aims to facilitate reproductive deci...
Programs of prospective carrier screening and genetic counseling for β-thalassemia among couples pla...
This study was designed to asses the Persian-American Jewish community’s perceptions of the risk of ...
The primary goal of carrier screening is to identify asymptomatic individuals who carry variants ass...
Introduction: Tay Sachs Disease (TSD) is a fatal genetic disorder with autosomal recessive inheritan...
CONTEXT: Tay-Sachs disease is an autosomal recessive disease characterized by progressive neurologic...
Tay-Sachs disease is a fatal genetic disease affecting Jewish infants of eastern European ancestry. ...
Objective: To give recommendations to physicians and midwives providing pre-conception or prenatal c...
C1 - Journal Articles RefereedA screening programme for Tay Sachs disease (TSD) carrier status was i...
Carrier screening for autosomal recessive disorders aims to facilitate reproductive decision-making ...
Tay-Sachs disease (TSD) is a fatal, recessively inherited neurodegenerative condition of infancy and...
Reproductive carrier screening started in some countries in the 1970s for hemoglobinopathies and Tay...
In Yemen, the prevalence of sickle cell trait and b-thalassemia trait are high. The aim of this prem...
Background: Carrier screening for autosomal recessive disorders aims to facilitate reproductive deci...
One of the primary aims of the genetic counselor is the reduction in the number of children born wit...
Background: Carrier screening for autosomal recessive disorders aims to facilitate reproductive deci...
Programs of prospective carrier screening and genetic counseling for β-thalassemia among couples pla...
This study was designed to asses the Persian-American Jewish community’s perceptions of the risk of ...
The primary goal of carrier screening is to identify asymptomatic individuals who carry variants ass...
Introduction: Tay Sachs Disease (TSD) is a fatal genetic disorder with autosomal recessive inheritan...
CONTEXT: Tay-Sachs disease is an autosomal recessive disease characterized by progressive neurologic...