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satb2-associated syndrome (6) 6
satb2‐associated syndrome (6) 6
genetics & heredity (5) 5
index medicus (5) 5
satb2 (5) 5
abnormalities, multiple - genetics (4) 4
cleft-palate (4) 4
humans (4) 4
matrix attachment region binding proteins - genetics (4) 4
phenotypes (4) 4
syndrome (4) 4
transcription factors - genetics (4) 4
abnormalities, multiple - diagnosis (3) 3
amino acid sequence (3) 3
child, preschool (3) 3
female (3) 3
genetic aspects (3) 3
infant (3) 3
mutation (3) 3
phenotype (3) 3
adolescent (2) 2
analysis (2) 2
child (2) 2
deletion (2) 2
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differentiation (2) 2
gene (2) 2
genetic association studies - methods (2) 2
genotype-phenotype correlation (2) 2
genotypes (2) 2
hereditary diseases (2) 2
identification (2) 2
male (2) 2
neurodevelopmental disorders (2) 2
nonsense mutation (2) 2
osteoporosis (2) 2
patients (2) 2
teeth (2) 2
young adult (2) 2
1 microdeletion syndrome (1) 1
2q32 deletion syndrome (1) 1
2q32-q33 (1) 1
2q33 (1) 1
2q33.1 (1) 1
2q33.1 microdeletion syndrome (1) 1
abnormalities, multiple - pathology (1) 1
adult (1) 1
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chromosome deletion (1) 1
chromosomes, human, pair 2 (1) 1
cleft lip/palate (1) 1
cleft palate - genetics (1) 1
cleft palate - pathology (1) 1
coding (1) 1
codon (1) 1
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colorectal-cancer (1) 1
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glass syndrome (1) 1
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American Journal of Medical Genetics Part A, ISSN 1552-4825, 02/2017, Volume 173, Issue 2, pp. 327 - 337
Journal Article
Journal Article
American Journal of Medical Genetics Part A, ISSN 1552-4825, 04/2018, Volume 176, Issue 4, pp. 925 - 935
Journal Article
American Journal of Medical Genetics Part A, ISSN 1552-4825, 12/2018, Volume 176, Issue 12, pp. 2614 - 2622
Special AT‐rich sequence‐binding protein 2 (SATB2)‐associated syndrome (SAS) is characterized by alterations of SATB2. Its clinical features include... 
SATB2‐associated syndrome | de novo mutation | odontoma | dental anomaly | SATB2 | SATB2-associated syndrome | CLEFT-PALATE | GENE | GENETICS & HEREDITY | IDENTIFICATION | OSTEOPOROSIS | Phenotypes | Mesenchyme | Nonsense mutation | Teeth | Amino acid sequence | mRNA | Mutation | Patients | Cleft lip/palate
Journal Article
Special Care in Dentistry, ISSN 0275-1879, 03/2019, Volume 39, Issue 2, pp. 220 - 224
Journal Article
Human Mutation, ISSN 1059-7794, 2019, Volume 40, Issue 8, pp. 1013 - 1029
SATB2‐associated syndrome (SAS) is an autosomal dominant neurodevelopmental disorder caused by alterations in the SATB2 gene. Here we present a review of... 
SATB2‐associated syndrome | genotype‐phenotype correlation | pathogenic variants | SATB2 | whole exome sequencing | SATB2-associated syndrome | genotype-phenotype correlation | GENETICS & HEREDITY | Genetic aspects | Codon | Genes | Analysis | Animal models | Phenotypes | Reviews | Nonsense mutation | Coding | Stop codon | Neurodevelopmental disorders | Genotypes | Hereditary diseases
Journal Article
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