164 related articles for article (PubMed ID: 31064002)
1. Chromosomal Abnormalities in Patients with Intellectual Disability: A 21-Year Retrospective Study.
Belkady B; Elkhattabi L; Elkarhat Z; Zarouf L; Razoki L; Aboulfaraj J; Nassereddine S; Cadi R; Rouba H; Barakat A
Hum Hered; 2018; 83(5):274-282. PubMed ID: 31064002
[TBL] [Abstract][Full Text] [Related]
2. Cytogenetic Studies of Rwandan Pediatric Patients Presenting with Global Developmental Delay, Intellectual Disability and/or Multiple Congenital Anomalies.
Uwineza A; Hitayezu J; Jamar M; Caberg JH; Murorunkwere S; Janvier N; Bours V; Mutesa L
J Trop Pediatr; 2016 Feb; 62(1):38-45. PubMed ID: 26507407
[TBL] [Abstract][Full Text] [Related]
3. Cytogenetic analysis of 5572 patients referred for suspected chromosomal abnormalities in Morocco.
Aboussair N; Jaouad IC; Dequaqui SC; Sbiti A; Elkerch F; Yahya B; Natiq A; Sefiani A
Genet Test Mol Biomarkers; 2012 Jun; 16(6):569-73. PubMed ID: 22506488
[TBL] [Abstract][Full Text] [Related]
4. A cytogenetic study in a large population of intellectually disabled Indonesians.
Mundhofir FE; Winarni TI; van Bon BW; Aminah S; Nillesen WM; Merkx G; Smeets D; Hamel BC; Faradz SM; Yntema HG
Genet Test Mol Biomarkers; 2012 May; 16(5):412-7. PubMed ID: 22191675
[TBL] [Abstract][Full Text] [Related]
5. New insights in the interpretation of array-CGH: autism spectrum disorder and positive family history for intellectual disability predict the detection of pathogenic variants.
Cappuccio G; Vitiello F; Casertano A; Fontana P; Genesio R; Bruzzese D; Ginocchio VM; Mormile A; Nitsch L; Andria G; Melis D
Ital J Pediatr; 2016 Apr; 42():39. PubMed ID: 27072107
[TBL] [Abstract][Full Text] [Related]
6. Confirmation of chromosomal microarray as a first-tier clinical diagnostic test for individuals with developmental delay, intellectual disability, autism spectrum disorders and dysmorphic features.
Battaglia A; Doccini V; Bernardini L; Novelli A; Loddo S; Capalbo A; Filippi T; Carey JC
Eur J Paediatr Neurol; 2013 Nov; 17(6):589-99. PubMed ID: 23711909
[TBL] [Abstract][Full Text] [Related]
7. First report on chromosomal abnormalities in Eastern Morocco: Identification of a new case of a de novo partial trisomy 13q using single-nucleotide polymorphism array.
Elidrissi Errahhali M; Elidrissi Errahhali M; Ramdani S; Lhousni S; Benajiba N; Rkain M; Babakhouya A; Elouali A; Ghanam A; Amrani R; Messaoudi S; Ayyad A; Oneib B; Mimouni A; Saadi H; Allaoui S; Ouarzane M; Guichet A; Charif M; Boulouiz R; Bellaoui M
Arch Pediatr; 2024 Feb; 31(2):112-116. PubMed ID: 38262863
[TBL] [Abstract][Full Text] [Related]
8. An epidemiological and aetiological study of children with intellectual disability in Taiwan.
Hou JW; Wang TR; Chuang SM
J Intellect Disabil Res; 1998 Apr; 42 ( Pt 2)():137-43. PubMed ID: 9617697
[TBL] [Abstract][Full Text] [Related]
9. Association of structural and numerical anomalies of chromosome 22 in a patient with syndromic intellectual disability.
Naoufal R; Legendre M; Couet D; Gilbert-Dussardier B; Kitzis A; Bilan F; Harbuz R
Eur J Med Genet; 2016 Sep; 59(9):483-7. PubMed ID: 27452446
[TBL] [Abstract][Full Text] [Related]
10. Cytogenetic analysis of 4216 patients referred for suspected chromosomal abnormalities in Southeast Turkey.
Balkan M; Akbas H; Isi H; Oral D; Turkyilmaz A; Kalkanli S; Simsek S; Fidanboy M; Alp MN; Gedik A; Budak T
Genet Mol Res; 2010 Jun; 9(2):1094-103. PubMed ID: 20568054
[TBL] [Abstract][Full Text] [Related]
11. Cytogenetic profile in 1,921 cases of trisomy 21 syndrome.
Flores-Ramírez F; Palacios-Guerrero C; García-Delgado C; Morales-Jiménez AB; Arias-Villegas CM; Cervantes A; Morán-Barroso VF
Arch Med Res; 2015 Aug; 46(6):484-9. PubMed ID: 26314225
[TBL] [Abstract][Full Text] [Related]
12. Inattention and hyperactivity/impulsivity among children with attention-deficit/hyperactivity-disorder, autism spectrum disorder, and intellectual disability.
McClain MB; Hasty Mills AM; Murphy LE
Res Dev Disabil; 2017 Nov; 70():175-184. PubMed ID: 28957735
[TBL] [Abstract][Full Text] [Related]
13. Investigation of microdeletions in syndromic intellectual disability by MLPA in Iranian population.
Loghmani Khouzani H; Kariminejad A; Zamani G; Ghalandary M; Bozorgmehr B; Amirsalari S; Mojahedi F; Tonekaboni SH; Kariminejad R; Najmabadi H
Arch Iran Med; 2014 Jul; 17(7):471-4. PubMed ID: 24979557
[TBL] [Abstract][Full Text] [Related]
14. Chromosome Abnormalities Related to Reproductive and Sexual Development Disorders: A 5-Year Retrospective Study.
Benchikh S; Bousfiha A; Razoki L; Aboulfaraj J; Zarouf L; Elbakay C; Rifai LL; El Hamouchi A; Nassereddine S
Biomed Res Int; 2021; 2021():8893467. PubMed ID: 34036105
[TBL] [Abstract][Full Text] [Related]
15. Chromosomal Microarray Analysis as a First-Tier Clinical Diagnostic Test in Patients With Developmental Delay/Intellectual Disability, Autism Spectrum Disorders, and Multiple Congenital Anomalies: A Prospective Multicenter Study in Korea.
Jang W; Kim Y; Han E; Park J; Chae H; Kwon A; Choi H; Kim J; Son JO; Lee SJ; Hong BY; Jang DH; Han JY; Lee JH; Kim SY; Lee IG; Sung IK; Moon Y; Kim M; Park JH
Ann Lab Med; 2019 May; 39(3):299-310. PubMed ID: 30623622
[TBL] [Abstract][Full Text] [Related]
16. Cytogenetic surveillance of mentally-retarded school children in southern Taiwan.
Shiue CN; Lin YH; Kuan LC; Lii LM; Tsai WH; Chen YJ; Lin SJ; Kuo PL
J Formos Med Assoc; 2004 Mar; 103(3):218-24. PubMed ID: 15124050
[TBL] [Abstract][Full Text] [Related]
17. Chromosomal microarray analysis of Bulgarian patients with epilepsy and intellectual disability.
Peycheva V; Kamenarova K; Ivanova N; Stamatov D; Avdjieva-Tzavella D; Alexandrova I; Zhelyazkova S; Pacheva I; Dimova P; Ivanov I; Litvinenko I; Bozhinova V; Tournev I; Simeonov E; Mitev V; Jordanova A; Kaneva R
Gene; 2018 Aug; 667():45-55. PubMed ID: 29753047
[TBL] [Abstract][Full Text] [Related]
18. Cytogenetic and epidemiological profiles of Down syndrome in a Moroccan population: a report of 852 cases.
Jaouad IC; Cherkaoui Deqaqi S; Sbiti A; Natiq A; Elkerch F; Sefiani A
Singapore Med J; 2010 Feb; 51(2):133-6. PubMed ID: 20358152
[TBL] [Abstract][Full Text] [Related]
19. Cytogenetic studies in a selected group of mentally retarded children.
Moghe M; Patel ZM; Peter JJ; Ambani LM
Hum Genet; 1981; 58(2):184-7. PubMed ID: 6456981
[TBL] [Abstract][Full Text] [Related]
20. Comorbidities associated with genetic abnormalities in children with intellectual disability.
Chen JS; Yu WH; Tsai MC; Hung PL; Tu YF
Sci Rep; 2021 Mar; 11(1):6563. PubMed ID: 33753861
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]