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 *

140 related articles for article (PubMed ID: 21465664)

  • 21. Phenotypic spectrum associated with de novo and inherited deletions and duplications at 16p11.2 in individuals ascertained for diagnosis of autism spectrum disorder.
    Fernandez BA; Roberts W; Chung B; Weksberg R; Meyn S; Szatmari P; Joseph-George AM; Mackay S; Whitten K; Noble B; Vardy C; Crosbie V; Luscombe S; Tucker E; Turner L; Marshall CR; Scherer SW
    J Med Genet; 2010 Mar; 47(3):195-203. PubMed ID: 19755429
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Ocular Findings in the 16p11.2 Microdeletion Syndrome: A Case Report and Literature Review.
    Stingl CS; Jackson-Cook C; Couser NL
    Case Rep Pediatr; 2020; 2020():2031701. PubMed ID: 32373379
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Chemogenetic Activation of Prefrontal Cortex Rescues Synaptic and Behavioral Deficits in a Mouse Model of 16p11.2 Deletion Syndrome.
    Wang W; Rein B; Zhang F; Tan T; Zhong P; Qin L; Yan Z
    J Neurosci; 2018 Jun; 38(26):5939-5948. PubMed ID: 29853627
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Expanding the spectrum of microdeletion 4q21 syndrome: a partial phenotype with incomplete deletion of the minimal critical region and a new association with cleft palate and Pierre Robin sequence.
    Bhoj E; Halbach S; McDonald-McGinn D; Tan C; Lande R; Waggoner D; Zackai E
    Am J Med Genet A; 2013 Sep; 161A(9):2327-33. PubMed ID: 23913759
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [Molecular genetic analysis of a child with de novo 16p11.2 microdeletion].
    Zhuang J; Wang Y; Zeng S; Wang J; Jiang Y
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Nov; 37(11):1283-1286. PubMed ID: 33179241
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Diversity of Clinical and Molecular Characteristics in Korean Patients with 16p11.2 Microdeletion Syndrome.
    Han JY; Cho YG; Jo DS; Park J
    Int J Mol Sci; 2023 Dec; 25(1):. PubMed ID: 38203422
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Germline 16p11.2 Microdeletion Predisposes to Neuroblastoma.
    Egolf LE; Vaksman Z; Lopez G; Rokita JL; Modi A; Basta PV; Hakonarson H; Olshan AF; Diskin SJ
    Am J Hum Genet; 2019 Sep; 105(3):658-668. PubMed ID: 31474320
    [TBL] [Abstract][Full Text] [Related]  

  • 28. A 1.37-Mb 12p11.22-p11.21 deletion coincident with a 367-kb 22q11.2 duplication detected by array comparative genomic hybridization in an adolescent girl with autism and difficulty in self-care of menstruation.
    Chen CP; Lin SP; Chern SR; Wu PS; Su JW; Lee CC; Wang W
    Taiwan J Obstet Gynecol; 2014 Mar; 53(1):74-8. PubMed ID: 24767651
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Expanding the clinical spectrum of the 16p11.2 chromosomal rearrangements: three patients with syringomyelia.
    Schaaf CP; Goin-Kochel RP; Nowell KP; Hunter JV; Aleck KA; Cox S; Patel A; Bacino CA; Shinawi M
    Eur J Hum Genet; 2011 Feb; 19(2):152-6. PubMed ID: 20959866
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Three case reports of patients indicating the diversity of molecular and clinical features of 16p11.2 microdeletion anomaly.
    Szelest M; Stefaniak M; Ręka G; Jaszczuk I; Lejman M
    BMC Med Genomics; 2021 Mar; 14(1):76. PubMed ID: 33691695
    [TBL] [Abstract][Full Text] [Related]  

  • 31. 16p11.2 600 kb Duplications confer risk for typical and atypical Rolandic epilepsy.
    Reinthaler EM; Lal D; Lebon S; Hildebrand MS; Dahl HH; Regan BM; Feucht M; Steinböck H; Neophytou B; Ronen GM; Roche L; Gruber-Sedlmayr U; Geldner J; Haberlandt E; Hoffmann P; Herms S; Gieger C; Waldenberger M; Franke A; Wittig M; Schoch S; Becker AJ; Hahn A; Männik K; Toliat MR; Winterer G; ; Lerche H; Nürnberg P; Mefford H; Scheffer IE; Berkovic SF; Beckmann JS; ; ; Sander T; Jacquemont S; Reymond A; Zimprich F; Neubauer BA
    Hum Mol Genet; 2014 Nov; 23(22):6069-80. PubMed ID: 24939913
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Association between microdeletion and microduplication at 16p11.2 and autism.
    Weiss LA; Shen Y; Korn JM; Arking DE; Miller DT; Fossdal R; Saemundsen E; Stefansson H; Ferreira MA; Green T; Platt OS; Ruderfer DM; Walsh CA; Altshuler D; Chakravarti A; Tanzi RE; Stefansson K; Santangelo SL; Gusella JF; Sklar P; Wu BL; Daly MJ;
    N Engl J Med; 2008 Feb; 358(7):667-75. PubMed ID: 18184952
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Cognitive and behavioral characterization of 16p11.2 deletion syndrome.
    Hanson E; Nasir RH; Fong A; Lian A; Hundley R; Shen Y; Wu BL; Holm IA; Miller DT;
    J Dev Behav Pediatr; 2010 Oct; 31(8):649-57. PubMed ID: 20613623
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Atypical neural variability in carriers of 16p11.2 copy number variants.
    Al-Jawahiri R; Jones M; Milne E
    Autism Res; 2019 Sep; 12(9):1322-1333. PubMed ID: 31260176
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Brain MRI abnormalities and spectrum of neurological and clinical findings in three patients with proximal 16p11.2 microduplication.
    Filges I; Sparagana S; Sargent M; Selby K; Schlade-Bartusiak K; Lueder GT; Robichaux-Viehoever A; Schlaggar BL; Shimony JS; Shinawi M
    Am J Med Genet A; 2014 Aug; 164A(8):2003-12. PubMed ID: 24891046
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [Prenatal ultrasonographic manifestations and genetic analysis of eight fetuses with 16p11.2 microdeletions].
    Cai M; Huang H; Lin N; Su L; Wu X; Xie X; Li Y; Xu L
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2022 Feb; 39(2):227-230. PubMed ID: 35076926
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Microdeletions in 16p11.2 and 13q31.3 associated with developmental delay and generalized overgrowth.
    George AM; Taylor J; Love DR
    Genet Mol Res; 2012 Sep; 11(3):3133-7. PubMed ID: 23007991
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Unusual Trisomy X Phenotype Associated with a Concurrent Heterozygous 16p11.2 Deletion: Importance of an Integral Approach for Proper Diagnosis.
    González-Del Angel A; Alcántara-Ortigoza MA; Ramos S; Algara-Ramírez C; Hernández-Hernández MA; Saenger-Rivas L
    Int J Mol Sci; 2023 Sep; 24(19):. PubMed ID: 37834089
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Major Vault Protein, a Candidate Gene in 16p11.2 Microdeletion Syndrome, Is Required for the Homeostatic Regulation of Visual Cortical Plasticity.
    Ip JPK; Nagakura I; Petravicz J; Li K; Wiemer EAC; Sur M
    J Neurosci; 2018 Apr; 38(16):3890-3900. PubMed ID: 29540554
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Scoliosis and vertebral anomalies: additional abnormal phenotypes associated with chromosome 16p11.2 rearrangement.
    Al-Kateb H; Khanna G; Filges I; Hauser N; Grange DK; Shen J; Smyser CD; Kulkarni S; Shinawi M
    Am J Med Genet A; 2014 May; 164A(5):1118-26. PubMed ID: 24458548
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.