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Human Genetics, ISSN 0340-6717, 11/2017, Volume 136, Issue 11, pp. 1419 - 1429
Journal Article
Brain and Development, ISSN 0387-7604, 02/2019, Volume 41, Issue 2, pp. 223 - 223
Journal Article
Brain and Development, ISSN 0387-7604, 10/2018, Volume 40, Issue 9, pp. 824 - 826
Journal Article
Journal Article
BMC Medical Genetics, ISSN 1471-2350, 10/2017, Volume 18, Issue 1, pp. 119 - 5
Background: Chromosomal rearrangements involving 17q23 have been described rarely. Deletions at 17q23.1q23.2 have been reported in individuals with... 
Chromosomal disorders | Genomic rearrangements | Chromosomal microarray | 17q23.2q23.3 duplication | GENETICS & HEREDITY | Seizures - genetics | Chromosome Duplication | Humans | Learning Disorders - physiopathology | Male | Developmental Disabilities - genetics | Electroencephalography | Self-Injurious Behavior - diagnosis | Seizures - physiopathology | Psychomotor Disorders - genetics | Psychomotor Disorders - physiopathology | Ataxia - genetics | Child | Developmental Disabilities - diagnosis | Speech Disorders - diagnosis | Ataxia - physiopathology | Developmental Disabilities - physiopathology | Gene Expression | Learning Disorders - diagnosis | Speech Disorders - genetics | Seizures - diagnosis | Gene Dosage | Ataxia - diagnosis | Speech Disorders - physiopathology | Proteins - genetics | Self-Injurious Behavior - genetics | Phenotype | Self-Injurious Behavior - physiopathology | Psychomotor Disorders - diagnosis | Learning Disorders - genetics | Chromosomes, Human, Pair 17 - chemistry | Case studies | Chromosome abnormalities | Diagnosis | Research | Gene mutations | Growth rate | Intellectual disabilities | Hyperactivity | Diagnostic tests | Genes | Genomes | Chromosome rearrangements | Clubfoot | Skills | Learning disabilities | Behavior | Chromosomes | Age | Chromosome 17 | Seizures | Phenotypes | Congenital diseases | EEG | DNA microarrays | Motor skill learning | Speech | Gene duplication | Ankyrin | Mutation | Foot diseases | Brain injury
Journal Article
by Anazi, Shams and Anazi, Shams and Maddirevula, Sateesh and Maddirevula, Sateesh and Salpietro, Vincenzo and Salpietro, Vincenzo and Asi, Yasmine T and Asi, Yasmine T and Alsahli, Saud and Alsahli, Saud and Alhashem, Amal and Alhashem, Amal and Shamseldin, Hanan E and Shamseldin, Hanan E and AlZahrani, Fatema and AlZahrani, Fatema and Patel, Nisha and Patel, Nisha and Ibrahim, Niema and Ibrahim, Niema and Abdulwahab, Firdous M and Abdulwahab, Firdous M and Hashem, Mais and Hashem, Mais and Alhashmi, Nadia and Alhashmi, Nadia and Al Murshedi, Fathiya and Al Murshedi, Fathiya and Al Kindy, Adila and Al Kindy, Adila and Alshaer, Ahmad and Alshaer, Ahmad and Rumayyan, Ahmed and Rumayyan, Ahmed and Al Tala, Saeed and Al Tala, Saeed and Kurdi, Wesam and Kurdi, Wesam and Alsaman, Abdulaziz and Alsaman, Abdulaziz and Alasmari, Ali and Alasmari, Ali and Banu, Selina and Banu, Selina and Sultan, Tipu and Sultan, Tipu and Saleh, Mohammed M and Saleh, Mohammed M and Alkuraya, Hisham and Alkuraya, Hisham and Salih, Mustafa A and Salih, Mustafa A and Aldhalaan, Hesham and Aldhalaan, Hesham and Ben-Omran, Tawfeg and Ben-Omran, Tawfeg and Al Musafri, Fatima and Al Musafri, Fatima and Ali, Rehab and Ali, Rehab and Suleiman, Jehan and Suleiman, Jehan and Tabarki, Brahim and Tabarki, Brahim and El-Hattab, Ayman W and El-Hattab, Ayman W and Bupp, Caleb and Bupp, Caleb and Alfadhel, Majid and Alfadhel, Majid and Al Tassan, Nada and Al Tassan, Nada and Monies, Dorota and Monies, Dorota and Arold, Stefan T and Arold, Stefan T and Abouelhoda, Mohamed and Abouelhoda, Mohamed and Lashley, Tammaryn and Lashley, Tammaryn and Houlden, Henry and Houlden, Henry and Faqeih, Eissa and Faqeih, Eissa and Alkuraya, Fowzan S and Alkuraya, Fowzan S
Human Genetics, ISSN 0340-6717, 1/2018, Volume 137, Issue 1, pp. 105 - 109
Variant nomenclature discrepancy was identified in the article. 
Human Genetics | Gene Function | Molecular Medicine | Biomedicine | Metabolic Diseases | Medical colleges | Intellectual disabilities | Nomenclature
Journal Article