Turkey is among the most populous countries of the world, and has a young population structure. The rate of consanguinity has been approximately 20-25% for the last 25 years. Various studies have shown that high consanguinity can be a contributing factor to the high incidence of some rare autosomal recessive diseases. Hemoglobinopathies are an important health problem, and Turkey also has one of the highest incidences of phenylketonuria in the world. Training and education in medical genetics, established as a specialty since 1972, play an important role in the setting of genetic services and meeting public health problems. Prenatal and preimplantation diagnosis is available for a variety of fetal diseases. Key words: consanguinity, congeni...
Objective: The objective of this study was to explore consanguinity, consanguineous marriages, their...
BACKGROUNDS: While many studies agree that consanguinity increases the rate of congenital heart dise...
WOS: 000290454500006PubMed ID: 21221751A limited numbers of published studies evaluate the referral ...
WOS: 000328080800021PubMed: 24046181In Turkey, the rate of consanguineous marriage is quite high (22...
Cukurova, the southern part of Turkey on the Mediterranean is noted for hemoglobinopathies and these...
PubMedID: 17486511Hemoglobinopathies are the most common genetic diseases in Turkey. Sickle cell ane...
We examined the distribution and demographic characteristics of congenital anomalies in a Turkish pr...
PubMedID: 824359119750 school children, ages 6 to 15 years, were examined by the authors of this stu...
Purpose: The purpose of this study was to assess the educational needs of physicians relating to gen...
PURPOSE: The purpose of this study was to assess the educational needs of physicians relating to gen...
PubMedID: 19065329Hemoglobinopathies are the most common genetic diseases in Turkey. The incidence o...
Inborn errors of metabolism (IEM) are a heterogeneous group of genetic disorders present in all ethn...
Consanguineous unions have been associated with an increased susceptibility to various forms of inhe...
Hereditary hemoglobin disorders with thalassemia and sickle-cell anemia are the most common monogeni...
Abstract Background and Objective: Consanguinity increases the incidence of genetic disorders. The ...
Objective: The objective of this study was to explore consanguinity, consanguineous marriages, their...
BACKGROUNDS: While many studies agree that consanguinity increases the rate of congenital heart dise...
WOS: 000290454500006PubMed ID: 21221751A limited numbers of published studies evaluate the referral ...
WOS: 000328080800021PubMed: 24046181In Turkey, the rate of consanguineous marriage is quite high (22...
Cukurova, the southern part of Turkey on the Mediterranean is noted for hemoglobinopathies and these...
PubMedID: 17486511Hemoglobinopathies are the most common genetic diseases in Turkey. Sickle cell ane...
We examined the distribution and demographic characteristics of congenital anomalies in a Turkish pr...
PubMedID: 824359119750 school children, ages 6 to 15 years, were examined by the authors of this stu...
Purpose: The purpose of this study was to assess the educational needs of physicians relating to gen...
PURPOSE: The purpose of this study was to assess the educational needs of physicians relating to gen...
PubMedID: 19065329Hemoglobinopathies are the most common genetic diseases in Turkey. The incidence o...
Inborn errors of metabolism (IEM) are a heterogeneous group of genetic disorders present in all ethn...
Consanguineous unions have been associated with an increased susceptibility to various forms of inhe...
Hereditary hemoglobin disorders with thalassemia and sickle-cell anemia are the most common monogeni...
Abstract Background and Objective: Consanguinity increases the incidence of genetic disorders. The ...
Objective: The objective of this study was to explore consanguinity, consanguineous marriages, their...
BACKGROUNDS: While many studies agree that consanguinity increases the rate of congenital heart dise...
WOS: 000290454500006PubMed ID: 21221751A limited numbers of published studies evaluate the referral ...