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Journal of cellular physiology, ISSN 0021-9541, 05/2018, Volume 233, Issue 5, pp. 4194 - 4204
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Oncotarget, ISSN 1949-2553, 04/2018, Volume 9, Issue 27, pp. 18929 - 18938
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Genes & diseases, ISSN 2352-3042, 10/2020
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Gene, ISSN 0378-1119, 02/2018, Volume 644, pp. 13 - 19
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Journal of neuroscience methods, ISSN 0165-0270, 11/2017, Volume 291, pp. 113 - 121
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Molecular neurobiology, ISSN 0893-7648, 04/2017, pp. 1 - 16
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Two types of primary mucinous ovarian tumors can be distinguished based on their origin
Modern pathology, ISSN 0893-3952, 04/2020, Volume 33, Issue 4, pp. 722 - 733
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American journal of medical genetics. Part A, ISSN 1552-4825, 12/2018, Volume 176, Issue 12, pp. 2614 - 2622
SATB2‐associated syndrome | de novo mutation | odontoma | dental anomaly | SATB2 | SATB2-associated syndrome | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Phenotypes | Mesenchyme | Nonsense mutation | Teeth | Amino acid sequence | mRNA | Mutation | Patients | Cleft lip/palate | Index Medicus
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Human mutation, ISSN 1059-7794, 2019, Volume 40, Issue 8, pp. 1013 - 1029
SATB2‐associated syndrome | genotype‐phenotype correlation | pathogenic variants | SATB2 | whole exome sequencing | SATB2-associated syndrome | genotype-phenotype correlation | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Genetic Association Studies | Humans | Child, Preschool | Male | Neurodevelopmental Disorders - genetics | Mutation, Missense | Transcription Factors - genetics | Animals | Gene Rearrangement | Matrix Attachment Region Binding Proteins - genetics | Adolescent | Female | Polymorphism, Single Nucleotide | Mutation | Codon, Terminator | Child | Disease Models, Animal | Genetic aspects | Codon | Genes | Analysis | Animal models | Phenotypes | Reviews | Nonsense mutation | Coding | Stop codon | Neurodevelopmental disorders | Genotypes | Hereditary diseases | Index Medicus
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Histopathology, ISSN 0309-0167, 1/2020, Volume 76, Issue 2, pp. 251 - 264
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Nature (London), ISSN 0028-0836, 02/2017, Volume 542, Issue 7642, pp. 433 - 438
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Prevalence | Humans | Middle Aged | Parents | Male | Mi-2 Nucleosome Remodeling and Deacetylase Complex - genetics | Developmental Disabilities - genetics | Casein Kinase II - genetics | Autoantigens - genetics | Young Adult | ras GTPase-Activating Proteins - genetics | Adult | Female | Child | CDC2 Protein Kinase - genetics | Histone-Lysine N-Methyltransferase - genetics | Repressor Proteins - genetics | Sex Characteristics | Transcription Factors - genetics | DNA-Binding Proteins - genetics | Mutation - genetics | Nerve Tissue Proteins - genetics | Sequence Analysis, DNA | Homeodomain Proteins - genetics | DEAD-box RNA Helicases - genetics | Exome - genetics | Phenotype | Myeloid-Lymphoid Leukemia Protein - genetics | Adolescent | Heredity - genetics | Protein Phosphatase 2C - genetics | Cohort Studies | Child development deviations | Genetic aspects | Genetic disorders | Developmental disabilities | Distribution | Genes | Families & family life | Births | Genomes | Mutation | Causality | Estimates | Age | Index Medicus | TRIO | MYT1L | EHMT1 | HNRNPU | SUV420H1 | COL4A3BP | SYNGAP1 | PPP2R1A | POGZ | EP300 | KCNH1 | SCN1A | MEF2C | CDKL5 | CSNK2A1 | DYRK1A | CASK | ALG13 | FOXP1 | KAT6B | TBL1XR1 | KAT6A | SCN8A | KCNQ2 | EEF1A2 | KCNQ3 | ADNP | PhenIcons | SET | KMT2A | ANKRD11 | STXBP1 | FOXG1 | ZC4H2 | ITPR1 | De novo mutation | Seizures | ZBTB18 | CREBBP | SMAD4 | PDHA1 | IQSEC2 | AUTS2 | BCL11A | BRAF | SMARCA2 | GRIN2B | MED13L | GNAO1 | CNOT3 | TCF4 | SCN2A | CDK13 | GABRB3 | SETD5 | KDM5B | Developmental Disease | DDX3X | CHD8 | PTEN | CHD4 | TCF20 | CTCF | CHD2 | WDR45 | SLC6A1 | MECP2 | CHAMP1 | KIF1A | Average Faces | MSL3 | PPP2R5D | SMC1A | ARID1B | DNM1 | CNKSR2 | PACS1 | WAC | ZMYND11 | AHDC1 | NFIX | SATB2 | HDAC8 | PPM1D | GNAI1 | PURA | PUF60 | NSD1 | Intellectual Disability | SLC35A2 | DYNC1H1 | NAA10 | USP9X | PTPN11 | GATAD2B | ASXL1 | KANSL1 | ASXL3 | CTNNB1 | QRICH1
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