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 *

181 related articles for article (PubMed ID: 29441129)

  • 21. Prenatal diagnosis of a 15q11.2-q14 deletion of paternal origin associated with increased nuchal translucency, mosaicism for de novo multiple unbalanced translocations involving 15q11-q14, 5qter, 15qter, 17pter and 3qter and Prader-Willi syndrome.
    Chen CP; Lin MH; Chen YY; Chern SR; Wu PS; Chen SW; Wu FT; Town DD; Lee MS; Pan CW; Wang W
    Taiwan J Obstet Gynecol; 2021 Mar; 60(2):335-340. PubMed ID: 33678338
    [TBL] [Abstract][Full Text] [Related]  

  • 22. A rare familial rearrangement of chromosomes 9 and 15 associated with intellectual disability: a clinical and molecular study.
    Lemskaya NA; Romanenko SA; Rezakova MA; Filimonova EA; Prokopov DY; Dolskiy AA; Perelman PL; Maksimova YV; Shorina AR; Yudkin DV
    Mol Cytogenet; 2021 Oct; 14(1):47. PubMed ID: 34607577
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Copy number changes and methylation patterns in an isodicentric and a ring chromosome of 15q11-q13: report of two cases and review of literature.
    Wang Q; Wu W; Xu Z; Luo F; Zhou Q; Li P; Xie J
    Mol Cytogenet; 2015; 8():97. PubMed ID: 26697114
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Screening for genomic rearrangements and methylation abnormalities of the 15q11-q13 region in autism spectrum disorders.
    Depienne C; Moreno-De-Luca D; Heron D; Bouteiller D; Gennetier A; Delorme R; Chaste P; Siffroi JP; Chantot-Bastaraud S; Benyahia B; Trouillard O; Nygren G; Kopp S; Johansson M; Rastam M; Burglen L; Leguern E; Verloes A; Leboyer M; Brice A; Gillberg C; Betancur C
    Biol Psychiatry; 2009 Aug; 66(4):349-59. PubMed ID: 19278672
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Tetrasomy 15q11-q13 diagnosed by FISH in a patient with autistic disorder.
    Ouldim K; Natiq A; Jonveaux P; Sefiani A
    J Biomed Biotechnol; 2007; 2007(3):61538. PubMed ID: 17541469
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Multiple forms of atypical rearrangements generating supernumerary derivative chromosome 15.
    Wang NJ; Parokonny AS; Thatcher KN; Driscoll J; Malone BM; Dorrani N; Sigman M; LaSalle JM; Schanen NC
    BMC Genet; 2008 Jan; 9():2. PubMed ID: 18177502
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Autism or atypical autism in maternally but not paternally derived proximal 15q duplication.
    Cook EH; Lindgren V; Leventhal BL; Courchesne R; Lincoln A; Shulman C; Lord C; Courchesne E
    Am J Hum Genet; 1997 Apr; 60(4):928-34. PubMed ID: 9106540
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Prenatal diagnosis of mosaic ring chromosome 22 associated with cardiovascular abnormalities and intrauterine growth restriction.
    Chen CP; Chern SR; Chang TY; Lee CC; Chen LF; Tzen CY; Wang W; Lin CJ; Yang BP; Yang LS
    Prenat Diagn; 2003 Jan; 23(1):40-3. PubMed ID: 12533811
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Williams Syndrome and 15q Duplication: Coincidence versus Association.
    Khokhar A; Agarwal S; Perez-Colon S
    Mol Syndromol; 2017 Jan; 8(1):50-54. PubMed ID: 28232784
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Detailed analysis of an idic(Y)(q11.21) in a mosaic karyotype.
    Al-Achkar W; Wafa A; Liehr T; Klein E; Moassass F
    Mol Med Rep; 2012 Aug; 6(2):293-6. PubMed ID: 22664581
    [TBL] [Abstract][Full Text] [Related]  

  • 31. A Familial Small Supernumerary Marker Chromosome 15 Associated with Cryptic Mosaicism with Two Different Additional Marker Chromosomes Derived de novo from Chromosome 9: Detailed Case Study and Implications for Recurrent Pregnancy Loss.
    Čulić V; Lasan-Trcić R; Liehr T; Lebedev IN; Pivić M; Pavelic J; Vulić R
    Cytogenet Genome Res; 2018; 156(4):179-184. PubMed ID: 30466092
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Three probands with autistic disorder and isodicentric chromosome 15.
    Wolpert CM; Menold MM; Bass MP; Qumsiyeh MB; Donnelly SL; Ravan SA; Vance JM; Gilbert JR; Abramson RK; Wright HH; Cuccaro ML; Pericak-Vance MA
    Am J Med Genet; 2000 Jun; 96(3):365-72. PubMed ID: 10898916
    [TBL] [Abstract][Full Text] [Related]  

  • 33. De Novo Mosaic 6p23-p25.3 Tetrasomy Caused by a Small Supernumerary Marker Chromosome Presenting Trisomy Distal 6p Phenotype: A Case Report and Literature Review.
    Syu YM; Ma JY; Ou TH; Lee CL; Lin HY; Lin SP; Lee CJ; Chen CP
    Diagnostics (Basel); 2022 Sep; 12(10):. PubMed ID: 36291995
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Characterization of an autism-associated segmental maternal heterodisomy of the chromosome 15q11-13 region.
    Kwasnicka-Crawford DA; Roberts W; Scherer SW
    J Autism Dev Disord; 2007 Apr; 37(4):694-702. PubMed ID: 17006779
    [TBL] [Abstract][Full Text] [Related]  

  • 35. A new case of mosaicism for invdup(15) duplicated for Prader-Willi/Angelman syndrome critical region (PWACR) in an adult healthy man.
    Guanciali-Franchi P; Calabrese G; Morizio E; Gatta V; Palka C; Stuppia L; Zuffardi O
    Eur J Med Genet; 2008; 51(3):239-44. PubMed ID: 18378203
    [TBL] [Abstract][Full Text] [Related]  

  • 36. A case of isodicentric chromosome 15 presented with epilepsy and developmental delay.
    Kim JS; Park J; Min BJ; Oh SK; Choi JS; Woo MJ; Chae JH; Kim KJ; Hwang YS; Lim BC
    Korean J Pediatr; 2012 Dec; 55(12):487-90. PubMed ID: 23300505
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Unique karyotypes in two patients with Prader-Willi syndrome.
    Narahara K; Hiramoto K; Murakami M; Miyake S; Tsuji K; Yokoyama Y; Namba H; Ninomiya S; Murakami R; Seino Y
    Am J Med Genet; 1992 Mar; 42(5):671-7. PubMed ID: 1632436
    [TBL] [Abstract][Full Text] [Related]  

  • 38. 15q duplication associated with autism in a multiplex family with a familial cryptic translocation t(14;15)(q11.2;q13.3) detected using array-CGH.
    Koochek M; Harvard C; Hildebrand MJ; Van Allen M; Wingert H; Mickelson E; Holden JJ; Rajcan-Separovic E; Lewis ME
    Clin Genet; 2006 Feb; 69(2):124-34. PubMed ID: 16433693
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Tetrasomy 15q11-q13 identified by fluorescence in situ hybridization in a patient with autistic disorder.
    Silva AE; Vayego-Lourenco SA; Fett-Conte AC; Goloni-Bertollo EM; Varella-Garcia M
    Arq Neuropsiquiatr; 2002 Jun; 60(2-A):290-4. PubMed ID: 12068363
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Molecular cytogenetic characterization of an inv dup(15) chromosome presenting as a small supernumerary marker chromosome associated with the inv dup(15) syndrome.
    Chen CP; Lin SP; Chern SR; Wu PS; Chen YN; Chen SW; Lee CC; Town DD; Yang CW; Wang W
    Taiwan J Obstet Gynecol; 2016 Oct; 55(5):728-732. PubMed ID: 27751425
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.