179 related articles for article (PubMed ID: 15264291)
1. Inverted duplication of 15q with terminal deletion in a multiple malformed newborn with intrauterine growth failure and lethal phenotype.
Genesio R; De Brasi D; Conti A; Borghese A; Di Micco P; Di Costanzo P; Paladini D; Ungaro P; Nitsch L
Am J Med Genet A; 2004 Aug; 128A(4):422-8. PubMed ID: 15264291
[TBL] [Abstract][Full Text] [Related]
2. Prenatal detection of a de novo terminal inverted duplication 4p in a fetus with the Wolf-Hirschhorn syndrome phenotype.
Beaujard MP; Jouannic JM; Bessières B; Borie C; Martin-Luis I; Fallet-Bianco C; Portnoï MF
Prenat Diagn; 2005 Jun; 25(6):451-5. PubMed ID: 15966060
[TBL] [Abstract][Full Text] [Related]
3. Recurrent inverted duplication of 2p with terminal deletion in a patient with the classical phenotype of trisomy 2p23-pter.
Gruchy N; Jacquemont ML; Lyonnet S; Labrune P; El Kamel I; Siffroi JP; Portnoï MF
Am J Med Genet A; 2007 Oct; 143A(20):2417-22. PubMed ID: 17853488
[TBL] [Abstract][Full Text] [Related]
4. Molecular characterization of a ring chromosome 15 in a fetus with intra uterine growth retardation and diaphragmatic hernia.
Hatem E; Meriam BR; Walid D; Adenen M; Moez G; Ali S
Prenat Diagn; 2007 May; 27(5):471-4. PubMed ID: 17380471
[TBL] [Abstract][Full Text] [Related]
5. Perinatal findings and molecular cytogenetic analysis of de novo partial trisomy 16q (16q22.1-->qter) and partial monosomy 20q (20q13.3-->qter).
Chen CP; Lin SP; Lin CC; Li YC; Chern SR; Chen WM; Lee CC; Hsieh LJ; Wang W
Prenat Diagn; 2005 Feb; 25(2):112-8. PubMed ID: 15712324
[TBL] [Abstract][Full Text] [Related]
6. Detection of mutually exclusive mosaicism in a girl with genotype-phenotype discrepancies.
Luo M; Mulchandani S; Dubbs HA; Swarr D; Pyle L; Zackai EH; Spinner NB; Conlin LK
Am J Med Genet A; 2015 Dec; 167A(12):3091-5. PubMed ID: 26198585
[TBL] [Abstract][Full Text] [Related]
7. Partial trisomy 15q: report of a patient and literature review.
Chandler K; Schrander-Stumpel CT; Engelen J; Theunissen P; Fryns JP
Genet Couns; 1997; 8(2):91-7. PubMed ID: 9219006
[TBL] [Abstract][Full Text] [Related]
8. Postnatal overgrowth by 15q-trisomy and intrauterine growth retardation by 15q-monosomy due to familial translocation t(13;15): dosage effect of IGF1R?
Nagai T; Shimokawa O; Harada N; Sakazume S; Ohashi H; Matsumoto N; Obata K; Yoshino A; Murakami N; Murai T; Sakuta R; Niikawa N
Am J Med Genet; 2002 Nov; 113(2):173-7. PubMed ID: 12407708
[TBL] [Abstract][Full Text] [Related]
9. Partial trisomy 8q and partial monosomy 15q associated with congenital hydrocephalus, diaphragmatic hernia, urinary tract anomalies, congenital heart defect and kyphoscoliosis.
Chen CP; Lee CC; Pan CW; Kir TY; Chen BF
Prenat Diagn; 1998 Dec; 18(12):1289-93. PubMed ID: 9885021
[TBL] [Abstract][Full Text] [Related]
10. Inverted duplication deletion of 8P: characterization by standard cytogenetic and SNP array analyses.
Sireteanu A; Braha E; Popescu R; Gramescu M; Gorduza EV; Rusu C
Rev Med Chir Soc Med Nat Iasi; 2013; 117(3):731-4. PubMed ID: 24502041
[TBL] [Abstract][Full Text] [Related]
11. 5.78 Mb terminal deletion of chromosome 15q in a girl, evaluation of NR2F2 as candidate gene for congenital heart defects.
Nakamura E; Makita Y; Okamoto T; Nagaya K; Hayashi T; Sugimoto M; Manabe H; Taketazu G; Kajino H; Fujieda K
Eur J Med Genet; 2011; 54(3):354-6. PubMed ID: 21172461
[TBL] [Abstract][Full Text] [Related]
12. Array based characterization of a terminal deletion involving chromosome subband 15q26.2: an emerging syndrome associated with growth retardation, cardiac defects and developmental delay.
Davidsson J; Collin A; Björkhem G; Soller M
BMC Med Genet; 2008 Jan; 9():2. PubMed ID: 18194513
[TBL] [Abstract][Full Text] [Related]
13. Overgrowth and trisomy 15q26.1-qter including the IGF1 receptor gene: report of two families and review of the literature.
Faivre L; Gosset P; Cormier-Daire V; Odent S; Amiel J; Giurgea I; Nassogne MC; Pasquier L; Munnich A; Romana S; Prieur M; Vekemans M; De Blois MC; Turleau C
Eur J Hum Genet; 2002 Nov; 10(11):699-706. PubMed ID: 12404101
[TBL] [Abstract][Full Text] [Related]
14. Tetrasomy 15q25.2→qter identified with SNP microarray in a patient with multiple anomalies including complex cardiovascular malformation.
George-Abraham JK; Zimmerman SL; Hinton RB; Marino BS; Witte DP; Hopkin RJ
Am J Med Genet A; 2012 Aug; 158A(8):1971-6. PubMed ID: 22711292
[TBL] [Abstract][Full Text] [Related]
15. Terminal 6.9 Mb deletion of chromosome 15q, associated with a structurally abnormal X chromosome in a patient with congenital diaphragmatic hernia and heart defect.
Jaillard S; Loget P; Lucas J; Dubourg C; Le Bouar G; Demurger F; Bertorello I; David V; Poulain P; Odent S; Belaud-Rotureau MA
Eur J Med Genet; 2011; 54(2):186-8. PubMed ID: 21115145
[TBL] [Abstract][Full Text] [Related]
16. Detection of an unexpected subtelomeric 15q26.2 --> qter deletion in a little girl: clinical and cytogenetic studies.
Pinson L; Perrin A; Plouzennec C; Parent P; Metz C; Collet M; Le Bris MJ; Douet-Guilbert N; Morel F; De Braekeleer M
Am J Med Genet A; 2005 Oct; 138A(2):160-5. PubMed ID: 16114049
[TBL] [Abstract][Full Text] [Related]
17. Congenital glaucoma and Silver-Russell phenotype associated with partial trisomy 7q and monosomy 15q.
Kato R; Kishibayashi J; Shimokawa O; Harada N; Niikawa N; Matsumoto N
Am J Med Genet; 2001 Dec; 104(4):319-22. PubMed ID: 11754068
[TBL] [Abstract][Full Text] [Related]
18. Molecular cytogenetic determination of a deletion/duplication of 1q that results in a trisomy 18 syndrome-like phenotype.
Mewar R; Harrison W; Weaver DD; Palmer C; Davee MA; Overhauser J
Am J Med Genet; 1994 Aug; 52(2):178-83. PubMed ID: 7802005
[TBL] [Abstract][Full Text] [Related]
19. A rare case of trisomy 15pter-q21.2 due to a de novo marker chromosome.
Pacanaro AN; Christofolini DM; Kulikowski LD; Belangero SI; da Silva Bellucco FT; Varela MC; Koiffmann CP; Yoshimoto M; Squire JA; Schiavon AV; Heck B; Melaragno MI
Am J Med Genet A; 2010 Mar; 152A(3):753-8. PubMed ID: 20186782
[TBL] [Abstract][Full Text] [Related]
20. A case of partial trisomy 2p23-pter syndrome with trisomy 18p due to a de novo supernumerary marker chromosome.
Lee JH; Cho HS; Lee ES; Jung BC
Korean J Lab Med; 2010 Jun; 30(3):312-7. PubMed ID: 20603594
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
