425 related articles for article (PubMed ID: 18236428)
1. Larsen-like phenotype associated with partial trisomy 3p and monosomy 5p.
Goumy C; Beaufrère AM; Tchirkov A; Gouas L; Gaspard F; Giollant M; Roucaute T; Veronèse L; Lemery D; Vago P
Prenat Diagn; 2008 Feb; 28(2):131-4. PubMed ID: 18236428
[TBL] [Abstract][Full Text] [Related]
2. Stillborn baby with partial monosomy of the short arm of chromosome 5 and partial trisomy of the short arm of chromosome 20.
Okada M; Usami A; Okajima K; Yamada M; Yamaguchi Y; Umezaki I; Matsuda Y; Ohta H
Congenit Anom (Kyoto); 2005 Dec; 45(4):161-4. PubMed ID: 16359498
[TBL] [Abstract][Full Text] [Related]
3. Combined partial trisomy 3p/monosomy 5p resulting in sonographic abnormalities.
Entezami M; Coumbos A; Runkel S; Vogel M; Wegner R
Clin Genet; 1997 Aug; 52(2):96-9. PubMed ID: 9298744
[TBL] [Abstract][Full Text] [Related]
4. De novo monosomy 9p24.3-pter and trisomy 17q24.3-qter characterised by microarray comparative genomic hybridisation in a fetus with an increased nuchal translucency.
Brisset S; Kasakyan S; L'Herminé AC; Mairovitz V; Gautier E; Aubry MC; Benkhalifa M; Tachdjian G
Prenat Diagn; 2006 Mar; 26(3):206-13. PubMed ID: 16450348
[TBL] [Abstract][Full Text] [Related]
5. Prenatal diagnosis of partial trisomy 3p(3p23-->pter) and monosomy 7q(7q36-->qter) in a fetus with microcephaly alobar holoprosencephaly and cyclopia.
Chen CP; Devriendt K; Lee CC; Chen WL; Wang W; Wang TY
Prenat Diagn; 1999 Oct; 19(10):986-9. PubMed ID: 10521829
[TBL] [Abstract][Full Text] [Related]
6. Prenatal diagnosis of partial trisomy 14q (14q31.1-->qter) and partial monosomy 5p (5p13.2-->pter) associated with polyhydramnios, short limbs, micropenis and brain malformations.
Chen CP; Chern SR; Tsai EJ; Lee CC; Chen LF; Wang W
Genet Couns; 2009; 20(3):281-8. PubMed ID: 19852436
[No Abstract] [Full Text] [Related]
7. 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]
8. 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]
9. Unbalanced translocation (3;5)(q26.1;p14): a clinical report.
Rossi M; Di Micco P; Perone L; De Brasi D; Guzzetta V; Andreucci MV; Vega GR; Marzano MG; Iaccarino E; Andria G
Am J Med Genet; 2002 Jul; 110(4):353-8. PubMed ID: 12116209
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. 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]
12. Prader-Willi syndrome resulting from an unbalanced translocation: characterization by array comparative genomic hybridization.
Klein OD; Cotter PD; Albertson DG; Pinkel D; Tidyman WE; Moore MW; Rauen KA
Clin Genet; 2004 Jun; 65(6):477-82. PubMed ID: 15151506
[TBL] [Abstract][Full Text] [Related]
13. Prenatal diagnosis of partial trisomy 3p and partial monosomy 11q in a fetus with a Dandy-Walker variant and trigonocephaly.
Chen CP; Tzen CY; Chang TY; Lin CJ; Wang W; Lee CC; Town DD; Chen LF; Lee MS
Prenat Diagn; 2002 Dec; 22(12):1112-3. PubMed ID: 12454968
[No Abstract] [Full Text] [Related]
14. Unbalanced translocation in an adult patient with premature ovarian failure and mental retardation detected by spectral karyotyping and array-comparative genomic hybridization.
Guo QS; Qin SY; Zhou SF; He L; Ma D; Zhang YP; Xiong Y; Peng T; Cheng Y; Li XT
Eur J Clin Invest; 2009 Aug; 39(8):729-37. PubMed ID: 19515099
[TBL] [Abstract][Full Text] [Related]
15. Molecular studies of segmental aneusomy: FISHing for the atypical cry in del(5)(p15.3).
Hodge JC; Lawson-Yuen A; Stoler JM; Ligon AH
Cytogenet Genome Res; 2007; 119(1-2):15-20. PubMed ID: 18160776
[TBL] [Abstract][Full Text] [Related]
16. Recurrent proximal 18p monosomy and 18q trisomy in a family with a maternal pericentric inversion of chromosome 18.
Prabhakara K; Wyandt HE; Huang XL; Prasad KS; Ramadevi AR
Ann Genet; 2004; 47(3):297-303. PubMed ID: 15337476
[TBL] [Abstract][Full Text] [Related]
17. Monosomy 5p and trisomy 12p in a boy with familial balanced translocation.
Vasudevan PC; Parker MJ
Clin Dysmorphol; 2006 Apr; 15(2):85-7. PubMed ID: 16531734
[TBL] [Abstract][Full Text] [Related]
18. Identification of a subtle chromosomal translocation in a family with recurrent miscarriages and a child with multiple congenital anomalies. A case report.
Shaffer LG; Spikes AS; Macha M; Dunn R
J Reprod Med; 1996 May; 41(5):367-71. PubMed ID: 8725766
[TBL] [Abstract][Full Text] [Related]
19. Prenatal diagnosis of partial monosomy 18p(18p11.2-->pter) and trisomy 21q(21q22.3-->qter) with alobar holoprosencephaly and premaxillary agenesis.
Chen CP; Chern SR; Wang W; Lee CC; Chen WL; Chen LF; Chang TY; Tzen CY
Prenat Diagn; 2001 May; 21(5):346-50. PubMed ID: 11360273
[TBL] [Abstract][Full Text] [Related]
20. Proximal 5p trisomy resulting from a marker chromosome implicates band 5p13 in 5p trisomy syndrome.
Avansino JR; Dennis TR; Spallone P; Stock AD; Levin ML
Am J Med Genet; 1999 Nov; 87(1):6-11. PubMed ID: 10528239
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
