X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (16) 16
iran (15) 15
mutation (12) 12
female (11) 11
index medicus (10) 10
male (9) 9
alpha-thalassemia - genetics (8) 8
pregnancy (6) 6
adult (5) 5
diagnosis (5) 5
dna mutational analysis (5) 5
family (5) 5
genetics & heredity (5) 5
genotype (5) 5
hematology (5) 5
iran - epidemiology (5) 5
prenatal diagnosis (5) 5
prevalence (5) 5
α-thalassemia (5) 5
alpha-globins - genetics (4) 4
alpha-thalassemia - epidemiology (4) 4
deletion (4) 4
gene frequency (4) 4
genetic testing (4) 4
intellectual disability - genetics (4) 4
population (4) 4
thalassemia (4) 4
alpha-thalassemia - diagnosis (3) 3
beta-thalassemia (3) 3
biochemistry & molecular biology (3) 3
homozygote (3) 3
human genetics (3) 3
medicine, general & internal (3) 3
mental retardation (3) 3
polymorphism (3) 3
province (3) 3
spectrum (3) 3
adolescent (2) 2
alpha-thalassemia (2) 2
alpha-thalassemia mutations (2) 2
aneuploidy (2) 2
apolipoprotein e (2) 2
beta-thalassemia - diagnosis (2) 2
biomedicine (2) 2
child (2) 2
chromosomes (2) 2
consanguinity (2) 2
dna - genetics (2) 2
experience (2) 2
genes (2) 2
genes, recessive (2) 2
genetic aspects (2) 2
genetic variation (2) 2
genetics (2) 2
hematologic tests (2) 2
hemoglobin h - genetics (2) 2
identification (2) 2
intellectual disability (2) 2
metabolic diseases (2) 2
middle aged (2) 2
molecular medicine (2) 2
multiple sclerosis (2) 2
mutations (2) 2
pedigree (2) 2
phenotype (2) 2
polymerase chain reaction (2) 2
prenatal diagnosis - methods (2) 2
research (2) 2
retrospective studies (2) 2
β-thalassemia (2) 2
5q13 (1) 1
alleles (1) 1
alpha thalassemia (1) 1
alpha-thalassemia - physiopathology (1) 1
amniocentesis (1) 1
amniotic fluid (1) 1
analysis (1) 1
anemia - genetics (1) 1
animals (1) 1
anomalies (1) 1
arrays (1) 1
autism (1) 1
base sequence (1) 1
beta-globins - genetics (1) 1
beta-thalassemia - genetics (1) 1
beta-thalassemia - prevention & control (1) 1
binding-protein (1) 1
blood transfusion (1) 1
brain - metabolism (1) 1
brain - physiology (1) 1
care and treatment (1) 1
cathepsin-g (1) 1
cell cycle (1) 1
cells, cultured (1) 1
children (1) 1
chromosome disorders (1) 1
chromosome disorders - diagnosis (1) 1
chromosome mapping (1) 1
cognition disorders (1) 1
cognition disorders - genetics (1) 1
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Nature, ISSN 0028-0836, 10/2011, Volume 478, Issue 7367, pp. 57 - 63
Journal Article
Journal Article
Public Health Genomics, ISSN 1662-4246, 04/2006, Volume 9, Issue 2, pp. 93 - 97
For 14 years, Iranian scientists have worked to develop a national thalassemia prevention program. Although historically abortion was considered unacceptable... 
Original Paper | Prevention | Screening | Thalassemia | Prenatal diagnosis | Traits | screening | PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH | thalassemia | traits | MUTATION | GENETICS & HEREDITY | prenatal diagnosis | BETA-THALASSEMIA | prevention | DNA - genetics | Pregnancy | Iran | Humans | Prenatal Diagnosis | Female | Mutation | beta-Thalassemia - diagnosis
Journal Article
Haematologica, ISSN 0390-6078, 07/2007, Volume 92, Issue 7, pp. 992 - 993
alpha thalassemia (alpha-thal) is one of the most common hemoglobin (Hb) disorders in the world. alpha-globin genes are located on chromosome 16. The majority... 
Iran | α Thalassemia | Mutation | mutation | DIAGNOSIS | alpha thalassemia | HEMATOLOGY | Molecular Epidemiology | Gene Frequency | Hemoglobins, Abnormal - genetics | Humans | alpha-Thalassemia - epidemiology | alpha-Thalassemia - genetics | Iran - epidemiology
Journal Article
Hemoglobin, ISSN 0363-0269, 2009, Volume 33, Issue 3-4, pp. 235 - 241
One hundred and three patients from Gilan Province, Iran, presenting with hypochromic and microcytic anemia parameters without iron deficiency were included in... 
Gilan province | Mutation | α-Thalassemia (α-thal) | Iran | DNA Mutational Analysis | alpha-Globins - genetics | Base Sequence | Gene Frequency | Humans | Genotype | alpha-Thalassemia - genetics
Journal Article
Hemoglobin, ISSN 0363-0269, 2009, Volume 33, Issue 2, pp. 115 - 123
Two hundred and fifty-five patients from Mazandaran Province, Iran, all presenting with hypochromic and microcytic anemia, were selected for α-thalassemia... 
Mutation | α-Thalassemia (α-thal) | Iran | Mazandaran Province | Mazandaran province | α-thalassemia (othal) | Genetic Testing | DNA Mutational Analysis | alpha-Globins - genetics | Humans | Hematologic Tests | alpha-Thalassemia - epidemiology | alpha-Thalassemia - genetics | Iran - epidemiology
Journal Article
American Journal of Human Genetics, ISSN 0002-9297, 05/2008, Volume 82, Issue 5, p. 1158
Recent studies have shown that autosomal recessive mental retardation (ARMR) is extremely heterogeneous, and there is reason to believe that the number of... 
Proteins | Genes | Genomics | Mutation | Mental retardation | Chromosomes
Journal Article
Human Mutation, ISSN 1059-7794, 09/2007, Volume 28, Issue 9, pp. 874 - 881
Journal Article
Journal of the Pakistan Medical Association, ISSN 0030-9982, 04/2012, Volume 62, Issue 4, pp. 396 - 398
Journal Article
Journal Article
Pediatric Hematology and Oncology, ISSN 0888-0018, 7/2010, Volume 27, Issue 5, pp. 405 - 412
Journal Article
Blood, ISSN 0006-4971, 11/2004, Volume 104, Issue 11, pp. 781 - 781
Abstract Heterozygous mutations in the gene, ELA2, encoding neutrophil elastase, cause cyclic neutropenia and are the commonest cause of severe congenital... 
Journal Article