208 related articles for article (PubMed ID: 17582615)
1. Prenatal diagnosis and prenatal imaging features of fetal monosomy 1p36.
Lissauer D; Larkins SA; Sharif S; MacPherson L; Rhodes C; Kilby MD
Prenat Diagn; 2007 Sep; 27(9):874-8. PubMed ID: 17582615
[TBL] [Abstract][Full Text] [Related]
2. Monosomy 1p36 deletion syndrome.
Gajecka M; Mackay KL; Shaffer LG
Am J Med Genet C Semin Med Genet; 2007 Nov; 145C(4):346-56. PubMed ID: 17918734
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Prenatal detection of a 1p36 deletion in a fetus with multiple malformations and a review of the literature.
Faivre L; Morichon-Delvallez N; Viot G; Martinovic J; Pinson MP; Aubry JP; Raclin V; Edery P; Dumez Y; Munnich A; Vekemans M
Prenat Diagn; 1999 Jan; 19(1):49-53. PubMed ID: 10073907
[TBL] [Abstract][Full Text] [Related]
5. Monosomy 1p36.
Slavotinek A; Shaffer LG; Shapira SK
J Med Genet; 1999 Sep; 36(9):657-63. PubMed ID: 10507720
[TBL] [Abstract][Full Text] [Related]
6. Further delineation of deletion 1p36 syndrome in 60 patients: a recognizable phenotype and common cause of developmental delay and mental retardation.
Battaglia A; Hoyme HE; Dallapiccola B; Zackai E; Hudgins L; McDonald-McGinn D; Bahi-Buisson N; Romano C; Williams CA; Brailey LL; Zuberi SM; Carey JC
Pediatrics; 2008 Feb; 121(2):404-10. PubMed ID: 18245432
[TBL] [Abstract][Full Text] [Related]
7. Identification of proximal 1p36 deletions using array-CGH: a possible new syndrome.
Kang SH; Scheffer A; Ou Z; Li J; Scaglia F; Belmont J; Lalani SR; Roeder E; Enciso V; Braddock S; Buchholz J; Vacha S; Chinault AC; Cheung SW; Bacino CA
Clin Genet; 2007 Oct; 72(4):329-38. PubMed ID: 17850629
[TBL] [Abstract][Full Text] [Related]
8. Prenatal detection of full monosomy 21 in a fetus with increased nuchal translucency: molecular cytogenetic analysis and review of the literature.
Manolakos E; Peitsidis P; Eleftheriades M; Dedoulis E; Ziegler M; Orru S; Liehr T; Petersen MB
J Obstet Gynaecol Res; 2010 Apr; 36(2):435-40. PubMed ID: 20492403
[TBL] [Abstract][Full Text] [Related]
9. Partial monosomy of chromosome 1p36.3: characterization of the critical region and delineation of a syndrome.
Reish O; Berry SA; Hirsch B
Am J Med Genet; 1995 Dec; 59(4):467-75. PubMed ID: 8585567
[TBL] [Abstract][Full Text] [Related]
10. Subtelomeric rearrangements and 22q11.2 deletion syndrome in anomalous growth-restricted fetuses with normal or balanced G-banded karyotype.
Chen M; Hwu WL; Kuo SJ; Chen CP; Yin PL; Chang SP; Lee DJ; Chen TH; Wang BT; Lin CC
Ultrasound Obstet Gynecol; 2006 Dec; 28(7):939-43. PubMed ID: 17121426
[TBL] [Abstract][Full Text] [Related]
11. Prader-Willi-like phenotype: investigation of 1p36 deletion in 41 patients with delayed psychomotor development, hypotonia, obesity and/or hyperphagia, learning disabilities and behavioral problems.
D'Angelo CS; Da Paz JA; Kim CA; Bertola DR; Castro CI; Varela MC; Koiffmann CP
Eur J Med Genet; 2006; 49(6):451-60. PubMed ID: 16564757
[TBL] [Abstract][Full Text] [Related]
12. Chromosome 1p36 deletion syndrome: prenatal diagnosis, molecular cytogenetic characterization and fetal ultrasound findings.
Chen CP; Chen M; Su YN; Hsu CY; Tsai FJ; Chern SR; Wu PC; Lee CC; Wang W
Taiwan J Obstet Gynecol; 2010 Dec; 49(4):473-80. PubMed ID: 21199750
[TBL] [Abstract][Full Text] [Related]
13. Prenatal diagnosis of a fetus affected with Down syndrome and deletion 1p36 syndrome by fluorescence in situ hybridization and spectral karyotyping.
Hsieh LJ; Hsieh TC; Yeh GP; Lin MI; Chen M; Wang BB
Fetal Diagn Ther; 2004; 19(4):356-60. PubMed ID: 15192296
[TBL] [Abstract][Full Text] [Related]
14. Prenatal diagnosis of mosaicism for 11q terminal deletion.
Valduga M; Cannard VL; Philippe C; Romana S; Miton A; Droulle P; Foliguet B; Lecompte T; Jonveaux P
Eur J Med Genet; 2007; 50(6):475-81. PubMed ID: 17761465
[TBL] [Abstract][Full Text] [Related]
15. Prenatal diagnosis and molecular characterization of an interstitial 1q24.2q25.2 deletion.
Chaabouni M; Martinovic J; Sanlaville D; AttiƩ-Bittach T; Caillat S; Turleau C; Vekemans M; Morichon N
Eur J Med Genet; 2006; 49(6):487-93. PubMed ID: 17142120
[TBL] [Abstract][Full Text] [Related]
16. Prenatal diagnosis of monosomy 1p36: a focus on brain abnormalities and a review of the literature.
Campeau PM; Ah Mew N; Cartier L; Mackay KL; Shaffer LG; Der Kaloustian VM; Thomas MA
Am J Med Genet A; 2008 Dec; 146A(23):3062-9. PubMed ID: 19006213
[TBL] [Abstract][Full Text] [Related]
17. Monosomy 1p36 breakpoint junctions suggest pre-meiotic breakage-fusion-bridge cycles are involved in generating terminal deletions.
Ballif BC; Yu W; Shaw CA; Kashork CD; Shaffer LG
Hum Mol Genet; 2003 Sep; 12(17):2153-65. PubMed ID: 12915474
[TBL] [Abstract][Full Text] [Related]
18. Unexpected death of a 12 year old boy with monosomy 1p36.
Neumann LM; Polster T; Spantzel T; Bartsch O
Genet Couns; 2004; 15(1):19-26. PubMed ID: 15083695
[TBL] [Abstract][Full Text] [Related]
19. Sacrococcygeal teratoma in a fetus with prenatally diagnosed partial trisomy 10q (10q24.3-->qter) and partial monosomy 17p (p13.3-->pter).
Batukan C; Ozgun MT; Basbug M; Caglayan O; Dundar M; Murat N
Prenat Diagn; 2007 Apr; 27(4):365-8. PubMed ID: 17295347
[TBL] [Abstract][Full Text] [Related]
20. Prenatal diagnosis of the distal 11q deletion and review of the literature.
Chen CP; Chern SR; Chang TY; Tzen CY; Lee CC; Chen WL; Chen LF; Wang W
Prenat Diagn; 2004 Feb; 24(2):130-6. PubMed ID: 14974122
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]