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satb2-associated syndrome (11) 11
satb2 (9) 9
genetics & heredity (7) 7
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humans (5) 5
satb2‐associated syndrome (5) 5
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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
American Journal of Medical Genetics Part A, ISSN 1552-4825, 04/2018, Volume 176, Issue 4, pp. 925 - 935
Journal Article
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
Objective Identify, diagnose, and document oral clinical and radiographic evidence associated with the genetic condition known as special AT‐rich... 
SATB2‐associated syndrome | dental | SATB2-associated syndrome | Health care industry | Protein binding
Journal Article
by Qian, YQ and Liu, J and Yang, YM and Chen, M and Jin, CL and Chen, PL and Lei, YL and Pan, HY and Dong, MY
FRONTIERS IN GENETICS, ISSN 1664-8021, 07/2019, Volume 10, p. 630
Mutations of SATB2 (OMIM#608148) gene at 2q33.1 have been associated with the autosomal dominant SATB2-associated syndrome (SAS), which is still short of... 
chromosome microarray analysis | GENE | droplet digital PCR | QUANTIFICATION | SATB2 | mosaicism | GENETICS & HEREDITY | SATB2-associated syndrome | gap-PCR | Polymerase chain reaction | Mosaicism | Usage | Diagnosis | Research
Journal Article
Human Mutation, ISSN 1059-7794, 08/2019, 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... 
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
Frontiers in Molecular Neuroscience, ISSN 1662-5099, 02/2019, Volume 12, p. 33
Satb2-associated syndrome (SAS) is a genetic disorder that results from the deletion or mutation of one allele within the Satb2 locus. Patients with SAS show... 
Satb2 | Cerebral cortex | Satb2-associated syndrome | Mouse behavior | Hippocampus | cerebral cortex | hippocampus | CALLOSAL | DETERMINANT | PROJECTION NEURON IDENTITY | mouse behavior | TRANSCRIPTION FACTOR | NEUROSCIENCES
Journal Article
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