168 related articles for article (PubMed ID: 19653912)
1. Molecular cytogenetic characterisation of a mosaic add(12)(p13.3) with an inv dup(3)(q26.31 --> qter) detected in an autistic boy.
Carreira IM; Melo JB; Rodrigues C; Backx L; Vermeesch J; Weise A; Kosyakova N; Oliveira G; Matoso E
Mol Cytogenet; 2009 Aug; 2():16. PubMed ID: 19653912
[TBL] [Abstract][Full Text] [Related]
2. Inv dup del(10q): identification by fluorescence in situ hybridization and array comparative genomic hybridization in a fetus with two concurrent chromosomal rearrangements.
Chen CP; Chen M; Su YN; Huang JP; Ma GC; Chang SP; Chern SR; Chen YT; Su JW; Lee CC; Town DD; Wang W
Taiwan J Obstet Gynecol; 2012 Jun; 51(2):245-52. PubMed ID: 22795102
[TBL] [Abstract][Full Text] [Related]
3. Molecular cytogenetic characterization of Xp22.32→pter deletion and Xq26.3→qter duplication in a male fetus associated with 46,Y,rec(X)dup(Xq) inv(X)(p22.3q26.3), a hypoplastic left heart, short stature, and maternal X chromosome pericentric inversion.
Chen CP; Chen CY; Chern SR; Wu PS; Chen YN; Chen SW; Lee CC; Town DD; Lee MS; Yang CW; Wang W
Taiwan J Obstet Gynecol; 2016 Oct; 55(5):705-711. PubMed ID: 27751420
[TBL] [Abstract][Full Text] [Related]
4. Novel case of dup(3q) syndrome due to a de novo interstitial duplication 3q24-q26.31 with minimal overlap to the dup(3q) critical region.
Meins M; Hagh JK; Gerresheim F; Einhoff E; Olschewski H; Strehl H; Epplen JT
Am J Med Genet A; 2005 Jan; 132A(1):84-9. PubMed ID: 15551338
[TBL] [Abstract][Full Text] [Related]
5. Inv dup del(9p): prenatal diagnosis and molecular cytogenetic characterization by fluorescence in situ hybridization and array comparative genomic hybridization.
Chen CP; Su YN; Chern SR; Hsu CY; Tsai FJ; Wu PC; Lee CC; Chen YT; Lee MS; Wang W
Taiwan J Obstet Gynecol; 2011 Mar; 50(1):67-73. PubMed ID: 21482378
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Partial tetrasomy of chromosome 3q and mosaicism in a child with autism.
Oliveira G; Matoso E; Vicente A; Ribeiro P; Marques C; Ataíde A; Miguel T; Saraiva J; Carreira I
J Autism Dev Disord; 2003 Apr; 33(2):177-85. PubMed ID: 12757357
[TBL] [Abstract][Full Text] [Related]
8. The inv dup (15) or idic (15) syndrome (Tetrasomy 15q).
Battaglia A
Orphanet J Rare Dis; 2008 Nov; 3():30. PubMed ID: 19019226
[TBL] [Abstract][Full Text] [Related]
9. Prenatal diagnosis and molecular cytogenetic characterization of rec(10)dup(10p)inv(10)(p11.2q26.3) in a fetus associated with paternal pericentric inversion.
Chen CP; Ko TM; Su YN; Wang LK; Chern SR; Wu PS; Chen YN; Chen SW; Ko K; Lee CC; Chen LF; Yang CW; Wang W
Taiwan J Obstet Gynecol; 2016 Oct; 55(5):733-737. PubMed ID: 27751426
[TBL] [Abstract][Full Text] [Related]
10. Analphoid supernumerary marker chromosome characterized by aCGH and FISH as inv dup(3)(q25.33qter) de novo in a child with dysmorphic features and streaky pigmentation: case report.
Murthy SK; Malhotra AK; Jacob PS; Naveed S; Al-Rowaished EE; Mani S; Padariyakam S; Pramathan R; Nath R; Al-Ali MT; Al-Gazali L
Mol Cytogenet; 2008 Aug; 1():19. PubMed ID: 18700989
[TBL] [Abstract][Full Text] [Related]
11. Inv dup del(10p): Prenatal diagnosis and molecular cytogenetic characterization.
Chen CP; Ko TM; Wang LK; Chern SR; Wu PS; Chen SW; Wu FT; Chen LF; Wang W
Taiwan J Obstet Gynecol; 2019 Sep; 58(5):698-703. PubMed ID: 31542096
[TBL] [Abstract][Full Text] [Related]
12. Two mosaic terminal inverted duplications arising post-zygotically: Evidence for possible formation of neo-telomeres.
Daniel A; St Heaps L; Sylvester D; Diaz S; Peters G
Cell Chromosome; 2008 Mar; 7():1. PubMed ID: 18331649
[TBL] [Abstract][Full Text] [Related]
13. Molecular cytogenetic characterization of the first reported case of an inv dup (4p)(p15.1-pter) with a concomitant 4q35.1-qter deletion and normal parents.
Tassano E; Alpigiani MG; Salvati P; Gimelli S; Lorini R; Gimelli G
Gene; 2012 Dec; 511(2):338-40. PubMed ID: 23031810
[TBL] [Abstract][Full Text] [Related]
14. Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from inv dup(15).
Chen CP; Lin HY; Wang LK; Chern SR; Wu PS; Chen SW; Wu FT; Fran S; Chen YY; Town DD; Pan CW; Wang W
Taiwan J Obstet Gynecol; 2020 Jul; 59(4):580-585. PubMed ID: 32653133
[TBL] [Abstract][Full Text] [Related]
15. Mosaic 46,XY,dup(14) (q12q22.3)/46, XY at amniocentesis in a pregnancy associated with a favorable fetal outcome and cytogenetic discrepancy in various tissues.
Chen CP; Wu FT; Chen CY; Chen SW; Chern SR; Wu PS; Pan YT; Lee CC; Lee MS; Chen YY; Wang W
Taiwan J Obstet Gynecol; 2023 Mar; 62(2):343-347. PubMed ID: 36965906
[TBL] [Abstract][Full Text] [Related]
16. Mosaic deletion-duplication syndrome of chromosome 3: prenatal molecular cytogenetic diagnosis using cultured and uncultured amniocytes and association with fetoplacental discrepancy.
Chen CP; Su YN; Hsu CY; Chern SR; Lee CC; Chen YT; Chen WL; Wang W
Taiwan J Obstet Gynecol; 2011 Dec; 50(4):485-91. PubMed ID: 22212322
[TBL] [Abstract][Full Text] [Related]
17. Relatives with opposite chromosome constitutions, rec(10)dup(10p)inv(10)(p15.1q26.12) and rec(10)dup(10q)inv(10)(p15.1q26.12), due to a familial pericentric inversion.
Ciuladaite Z; Preiksaitiene E; Utkus A; Kučinskas V
Cytogenet Genome Res; 2014; 144(2):109-13. PubMed ID: 25401700
[TBL] [Abstract][Full Text] [Related]
18. A new case of dup(3q) syndrome due to a pure duplication of 3qter.
Faas BH; De Vries BB; Van Es-Van Gaal J; Merkx G; Draaisma JM; Smeets DF
Clin Genet; 2002 Oct; 62(4):315-20. PubMed ID: 12372060
[TBL] [Abstract][Full Text] [Related]
19. Interphase fluorescence in situ hybridization characterization of mosaicism using uncultured amniocytes and cultured stimulated cord blood lymphocytes in prenatally detected Pallister-Killian syndrome.
Chen CP; Peng CR; Chern SR; Kuo YL; Wu PS; Town DD; Pan CW; Yang CW; Wang W
Taiwan J Obstet Gynecol; 2014 Dec; 53(4):566-71. PubMed ID: 25510702
[TBL] [Abstract][Full Text] [Related]
20. The embryo battle against adverse genomes: Are de novo terminal deletions the rescue of unfavorable zygotic imbalances?
Zuffardi O; Fichera M; Bonaglia MC
Eur J Med Genet; 2022 Aug; 65(8):104532. PubMed ID: 35724817
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]