328 related articles for article (PubMed ID: 26088875)
1. Distal 10q trisomy with copy number gain in chromosome region 10q23.1-10q25.1: the Wnt signaling pathway is the most pertinent to the gene content in the region of copy number gain: a case report.
Wong SL; Chou HH; Chao CN; Leung JH; Chen YH; Hsu CD
BMC Res Notes; 2015 Jun; 8():250. PubMed ID: 26088875
[TBL] [Abstract][Full Text] [Related]
2. Prenatal diagnosis of sub-microscopic partial trisomy 10q using chromosomal microarray analysis in a phenotypically abnormal fetus with normal karyotype.
Browne PC; Adam S; Badr M; Brooks CR; Edwards J; Walker P; Mohamed S; Gregg AR
J Neonatal Perinatal Med; 2016 May; 9(2):217-22. PubMed ID: 27197934
[TBL] [Abstract][Full Text] [Related]
3. Partial trisomy of the distal part of 10q: a report of two Egyptian cases.
Aglan MS; Kamel AK; Helmy NA
Genet Couns; 2008; 19(2):199-209. PubMed ID: 18618995
[TBL] [Abstract][Full Text] [Related]
4. A rare case of trisomy 11q23.3-11q25 and trisomy 22q11.1-22q11.21.
Zou PS; Li HF; Chen LS; Ma M; Chen XH; Xue D; Cao DH
Genet Mol Res; 2016 May; 15(2):. PubMed ID: 27173335
[TBL] [Abstract][Full Text] [Related]
5. Subtelomeric 6.7 Mb trisomy 10p and 5.6 Mb monosomy 21q detected by FISH and array-CGH in three related patients.
Szabó GP; Knegt AC; Ujfalusi A; Balogh E; Szabó T; Oláh É
Am J Med Genet A; 2012 Apr; 158A(4):869-76. PubMed ID: 22407767
[TBL] [Abstract][Full Text] [Related]
6. Prenatal diagnosis and molecular cytogenetic analysis of partial monosomy 10q (10q25.3-->qter) and partial trisomy 18q (18q23-->qter) in a fetus associated with cystic hygroma and ambiguous genitalia.
Chen CP; Chern SR; Wang TH; Hsueh DW; Lee CC; Town DD; Wang W; Ko TM
Prenat Diagn; 2005 Jun; 25(6):492-6. PubMed ID: 15966044
[TBL] [Abstract][Full Text] [Related]
7. Clinical and cytogenetic features of a patient with partial trisomy 8q and partial monosomy 13q delineated by array comparative genomic hybridization.
Sohn YB; Yun JN; Park SJ; Park MS; Kim SH; Lee JH
Ann Clin Lab Sci; 2013; 43(3):332-6. PubMed ID: 23884231
[TBL] [Abstract][Full Text] [Related]
8. Distal trisomy of 10q with distal monosomy of 15q due to a paternal translocation.
Sun SC; Luo FW; Song HW; He JB; Peng YS
J Int Med Res; 2009; 37(4):1230-7. PubMed ID: 19761709
[TBL] [Abstract][Full Text] [Related]
9. A further patient with van Maldergem syndrome.
Neuhann TM; Müller D; Hackmann K; Holzinger S; Schrock E; Di Donato N
Eur J Med Genet; 2012 Jun; 55(6-7):423-8. PubMed ID: 22469822
[TBL] [Abstract][Full Text] [Related]
10. Complex distal 10q rearrangement in a girl with mild intellectual disability: follow up of the patient and review of the literature of non-acrocentric satellited chromosomes.
Sarri C; Douzgou S; Gyftodimou Y; Tümer Z; Ravn K; Pasparaki A; Sarafidou T; Kontos H; Kokotas H; Karadima G; Grigoriadou M; Pandelia E; Theodorou V; Moschonas NK; Petersen MB
Am J Med Genet A; 2011 Nov; 155A(11):2841-54. PubMed ID: 21964744
[TBL] [Abstract][Full Text] [Related]
11. Microduplications in 22q11.2 and 8q22.1 associated with mild mental retardation and generalized overgrowth.
Tarsitano M; Ceglia C; Novelli A; Capalbo A; Lombardo B; Pastore L; Fioretti G; Vicari L; Pisanti MA; Friso P; Cavaliere ML
Gene; 2014 Feb; 536(1):213-6. PubMed ID: 24315824
[TBL] [Abstract][Full Text] [Related]
12. Chromosomal 10Q26 trisomy resulting from paternal T(9;10)(PTER;Q26.1).
Hou JW
J Formos Med Assoc; 2003 Dec; 102(12):887-92. PubMed ID: 14976570
[TBL] [Abstract][Full Text] [Related]
13. Early renal insufficiency in a neonate with de novo partial trisomy of chromosome 10q.
Varda NM; Kokalj Vokac N; Kanic Z; Bracic K; Erjavec A; Zagradisnik B; Gregoric A
Am J Med Genet A; 2003 Dec; 123A(2):164-8. PubMed ID: 14598340
[TBL] [Abstract][Full Text] [Related]
14. De-novo 'pure' partial trisomy (6)(p22.3→pter): a case report and review of the literature.
Sivasankaran A; Murthy K; Oruganti VP; Deenadayalu A; R Samuel C; Kandukuri LR
Clin Dysmorphol; 2017 Jan; 26(1):26-32. PubMed ID: 27759572
[TBL] [Abstract][Full Text] [Related]
15. Deletion 21q22.3 and duplication 7q35q36.3 in a Colombian girl: a case report.
Ruiz-Botero F; Pachajoa H
J Med Case Rep; 2016 Jul; 10():204. PubMed ID: 27459995
[TBL] [Abstract][Full Text] [Related]
16. Chromosomal-array analysis reveals partial 11q duplication and partial 12p deletion in a mildly affected case.
Tuğ E; Yirmibeş Karaoğuz M; Kayhan G; Ergün MA; Perçin FE
Am J Med Genet A; 2014 Jul; 164A(7):1770-6. PubMed ID: 24677787
[TBL] [Abstract][Full Text] [Related]
17. Partial trisomy 3p and partial monosomy 11q associated with atrial septal defect, cleft palate, and developmental delay: a case report.
Tan EC; Lim E; Cham B; Knight L; Ng I
Cytogenet Genome Res; 2011; 134(4):319-24. PubMed ID: 21654159
[TBL] [Abstract][Full Text] [Related]
18. [Clinical and molecular cytogenetic analysis of a rare case of mosaicism for partial monosomy 3p and partial trisomy 10q in human].
Karamysheva TV; Matveeva VG; Shorina AP; Rubtsov NB
Genetika; 2001 Jun; 37(6):811-6. PubMed ID: 11517768
[TBL] [Abstract][Full Text] [Related]
19. Familial 9q22.3 microduplication spanning PTCH1 causes short stature syndrome with mild intellectual disability and dysmorphic features.
Izumi K; Hahn A; Christ L; Curtis C; Neilson DE
Am J Med Genet A; 2011 Jun; 155A(6):1384-9. PubMed ID: 21567912
[TBL] [Abstract][Full Text] [Related]
20. A severely mental and motor retarded boy with monosomy 9pter-->p22 trisomy 10q26-->qter due to paternal reciprocal translocation 46,XY,t(9;10)(p23;q26).
Akbas E; Polat S; Karakas-Celik S; Altintas ZM; Yildirim M; Yilgor E
Genet Couns; 2011; 22(4):417-23. PubMed ID: 22303803
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]