These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

175 related articles for article (PubMed ID: 25922617)

  • 21. [Detection of genomic copy number variations in patients with unexplained mental retardation/developmental delay by low coverage whole-genome sequencing].
    Song H; Shi P; Xiao Y; Hou Y; Chen D; Kong X
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Sep; 37(9):953-957. PubMed ID: 32820506
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Rare Copy Number Variations and Predictors in Children With Intellectual Disability and Epilepsy.
    Kessi M; Xiong J; Wu L; Yang L; He F; Chen C; Pang N; Duan H; Zhang W; Arafat A; Yin F; Peng J
    Front Neurol; 2018; 9():947. PubMed ID: 30510536
    [No Abstract]   [Full Text] [Related]  

  • 23. Recurrent benign copy number variants & issues in interpretation of variants of unknown significance identified by cytogenetic microarray in Indian patients with intellectual disability.
    Boggula VR; Agarwal M; Kumar R; Awasthi S; Phadke SR
    Indian J Med Res; 2015 Dec; 142(6):699-712. PubMed ID: 26831419
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Application of high resolution SNP arrays in patients with congenital oral clefts in south China.
    Lei TY; Wang HT; Li F; Cui YQ; Fu F; Li R; Liao C
    J Genet; 2016 Dec; 95(4):801-809. PubMed ID: 27994178
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Changing interpretation of chromosomal microarray over time in a community cohort with intellectual disability.
    Palmer E; Speirs H; Taylor PJ; Mullan G; Turner G; Einfeld S; Tonge B; Mowat D
    Am J Med Genet A; 2014 Feb; 164A(2):377-85. PubMed ID: 24311194
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Array-CGH increased the diagnostic rate of developmental delay or intellectual disability in Taiwan.
    Lee CL; Lee CH; Chuang CK; Chiu HC; Chen YJ; Chou CL; Wu PS; Chen CP; Lin HY; Lin SP
    Pediatr Neonatol; 2019 Aug; 60(4):453-460. PubMed ID: 30581099
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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]  

  • 28. Copy number variants analysis in a cohort of isolated and syndromic developmental delay/intellectual disability reveals novel genomic disorders, position effects and candidate disease genes.
    Di Gregorio E; Riberi E; Belligni EF; Biamino E; Spielmann M; Ala U; Calcia A; Bagnasco I; Carli D; Gai G; Giordano M; Guala A; Keller R; Mandrile G; Arduino C; Maffè A; Naretto VG; Sirchia F; Sorasio L; Ungari S; Zonta A; Zacchetti G; Talarico F; Pappi P; Cavalieri S; Giorgio E; Mancini C; Ferrero M; Brussino A; Savin E; Gandione M; Pelle A; Giachino DF; De Marchi M; Restagno G; Provero P; Cirillo Silengo M; Grosso E; Buxbaum JD; Pasini B; De Rubeis S; Brusco A; Ferrero GB
    Clin Genet; 2017 Oct; 92(4):415-422. PubMed ID: 28295210
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Benign, Pathogenic and Copy Number Variations of Unknown Clinical Significance in Patients with Congenital Malformations and Developmental Delay.
    Mihaylova M; Staneva R; Toncheva D; Pancheva M; Hadjidekova S
    Balkan J Med Genet; 2017 Jun; 20(1):5-12. PubMed ID: 28924535
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Genomic study via chromosomal microarray analysis in a group of Romanian patients with obesity and developmental disability/intellectual disability.
    Micleaa D; Al-Khzouza C; Osan S; Bucerzan S; Cret V; Popp RA; Puiu M; Chirita-Emandi A; Zimbru C; Ghervan C
    J Pediatr Endocrinol Metab; 2019 Jul; 32(7):667-674. PubMed ID: 31150357
    [TBL] [Abstract][Full Text] [Related]  

  • 31. 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]  

  • 32. Large De Novo Microdeletion in Epilepsy with Intellectual and Developmental Disabilities, with a Systems Biology Analysis.
    Gao K; Zhang Y; Zhang L; Kong W; Xie H; Wang J; Wu Y; Wu X; Liu X; Zhang Y; Zhang F; Yu AC; Jiang Y
    Adv Neurobiol; 2018; 21():247-266. PubMed ID: 30334225
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Case Report: Identification of a
    Tung Y; Lu H; Lin W; Huang T; Kim S; Hu G; Zhang G; Zheng G
    Front Genet; 2021; 12():648351. PubMed ID: 34093647
    [No Abstract]   [Full Text] [Related]  

  • 34. Copy number variants prioritization after array-CGH analysis - a cohort of 1000 patients.
    Carreira IM; Ferreira SI; Matoso E; Pires LM; Ferrão J; Jardim A; Mascarenhas A; Pinto M; Lavoura N; Pais C; Paiva P; Simões L; Caramelo F; Ramos L; Venâncio M; Ramos F; Beleza A; Sá J; Saraiva J; de Melo JB
    Mol Cytogenet; 2015; 8():103. PubMed ID: 26719768
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Obesity and developmental delay in a patient with uniparental disomy of chromosome 2.
    Yu T; Li J; Li N; Liu R; Ding Y; Chang G; Chen Y; Shen Y; Wang X; Wang J
    Int J Obes (Lond); 2016 Dec; 40(12):1935-1941. PubMed ID: 27654142
    [TBL] [Abstract][Full Text] [Related]  

  • 36. 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]  

  • 37. Identification of De Novo and Rare Inherited Copy Number Variants in Children with Syndromic Congenital Heart Defects.
    Hussein IR; Bader RS; Chaudhary AG; Bassiouni R; Alquaiti M; Ashgan F; Schulten HJ; Al Qahtani MH
    Pediatr Cardiol; 2018 Jun; 39(5):924-940. PubMed ID: 29541814
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Construction of copy number variation landscape and characterization of associated genes in a Bangladeshi cohort of neurodevelopmental disorders.
    Akter H; Rahman MM; Sarker S; Basiruzzaman M; Islam MM; Rahaman MA; Rahaman MA; Eshaque TB; Dity NJ; Sarker S; Amin MR; Hossain MM; Lopa M; Jahan N; Hossain S; Islam A; Mondol A; Faruk MO; Saha N; Kundu GK; Kanta SI; Kazal RK; Fatema K; Rahman MA; Hasan M; Hossain Mollah MA; Hosen MI; Karuvantevida N; Begum G; Zehra B; Nassir N; Nabi AHMN; Uddin KMF; Uddin M
    Front Genet; 2023; 14():955631. PubMed ID: 36959829
    [No Abstract]   [Full Text] [Related]  

  • 39. Chromosomal Microarray Analysis in Turkish Patients with Unexplained Developmental Delay and Intellectual Developmental Disorders.
    Gürkan H; Atli Eİ; Atli E; Bozatli L; Altay MA; Yalçintepe S; Özen Y; Eker D; Akurut Ç; Demır S; Görker I
    Noro Psikiyatr Ars; 2020 Sep; 57(3):177-191. PubMed ID: 32952419
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Genome-wide copy number variation analysis in idiopathic intellectual disability/multiple congenital anomalies.
    Pariltay E; Durmaz A; Durmaz B; Aykut A; Onay H; Ak H; Aydin HH; Ozkinay F; Cogulu O
    Genet Couns; 2014; 25(2):221-9. PubMed ID: 25059023
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.