These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
1247 related articles for article (PubMed ID: 15966060)
41. Prenatal diagnosis of a partial trisomy 13q (q14-->qter): phenotype, cytogenetics and molecular characterization by spectral karyotyping and array comparative genomic hybridization. Machado IN; Heinrich JK; Campanhol C; Rodrigues-Peres RM; Oliveira FM; Barini R Genet Mol Res; 2010 Mar; 9(1):441-8. PubMed ID: 20391329 [TBL] [Abstract][Full Text] [Related]
42. Prenatal diagnosis of concomitant Wolf-Hirschhorn syndrome and split hand-foot malformation associated with partial monosomy 4p (4p16.1-->pter) and partial trisomy 10q (10q25.1-->qter). Chen CP; Chen YJ; Chern SR; Tsai FJ; Chang TY; Lee CC; Town DD; Lee MS; Wang W Prenat Diagn; 2008 May; 28(5):450-3. PubMed ID: 18395879 [No Abstract] [Full Text] [Related]
43. 4p- syndrome and 9p tetrasomy mosaicism with cleft lip and palate. Kobayashi J; Kimijima Y; Yamada S; Amagasa T; Saito-Ohara F J Craniomaxillofac Surg; 2000 Jun; 28(3):165-70. PubMed ID: 10964553 [TBL] [Abstract][Full Text] [Related]
44. First clinical case of small de novo duplication of 19q (13.3-13.4) confirmed by FISH. Bhat M; Morrison PJ; Getty A; McManus D; Tubman R; Nevin NC Am J Med Genet; 2000 Mar; 91(3):201-3. PubMed ID: 10756343 [TBL] [Abstract][Full Text] [Related]
45. Two sibs with different phenotypes due to adjacent-1 segregation of a subtle translocation t(4;5)(p16.3;p15.3)mat. Qumsiyeh MB; Stevens CA Am J Med Genet; 1993 Sep; 47(3):387-91. PubMed ID: 8135287 [TBL] [Abstract][Full Text] [Related]
46. Prenatal diagnosis of de novo unbalanced translocation 8p;21q using subtelomeric probes. Ozkinay F; Kanit H; Onay H; Cogulu O; Gunduz C; Ercal D; Ozkinay C Genet Couns; 2006; 17(3):315-20. PubMed ID: 17100200 [TBL] [Abstract][Full Text] [Related]
47. 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]
48. 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]
49. Tandem duplication/deletion in a maternally derived chromosome 9 supernumerary derivative resulting in 9p trisomy and partial 9q tetrasomy. Wyandt HE; Lebo RV; Fenerci EY; Sadhu DN; Milunsky JM Am J Med Genet; 2000 Aug; 93(4):305-12. PubMed ID: 10946358 [TBL] [Abstract][Full Text] [Related]
50. A paternally derived inverted duplication of 7q with evidence of a telomeric deletion. Stetten G; Charity LL; Kasch LM; Scott AF; Berman CL; Pressman E; Blakemore KJ Am J Med Genet; 1997 Jan; 68(1):76-81. PubMed ID: 8986281 [TBL] [Abstract][Full Text] [Related]
51. Class II neocentromeres: a putative common neocentromere site in band 4q21.2. Warburton PC; Barwell J; Splitt M; Maxwell D; Bint S; Ogilvie CM Eur J Hum Genet; 2003 Oct; 11(10):749-53. PubMed ID: 14512964 [TBL] [Abstract][Full Text] [Related]
52. Effect of the size of the deletion and clinical manifestation in Wolf-Hirschhorn syndrome: analysis of 13 patients with a de novo deletion. Wieczorek D; Krause M; Majewski F; Albrecht B; Horn D; Riess O; Gillessen-Kaesbach G Eur J Hum Genet; 2000 Jul; 8(7):519-26. PubMed ID: 10909852 [TBL] [Abstract][Full Text] [Related]
53. Prenatal diagnosis of inherited satellited non-acrocentric chromosomes. Chen CP; Devriendt K; Chern SR; Lee CC; Wang W; Lin SP Prenat Diagn; 2000 May; 20(5):384-9. PubMed ID: 10820405 [TBL] [Abstract][Full Text] [Related]
54. Duplication of the Wolf-Hirschhorn syndrome critical region causes neurodevelopmental delay. Hannes F; Drozniewska M; Vermeesch JR; Haus O Eur J Med Genet; 2010; 53(3):136-40. PubMed ID: 20197130 [TBL] [Abstract][Full Text] [Related]
55. Prenatal diagnosis of a de novo complex chromosome rearrangement (CCR) mediated by six breakpoints, and a review of 20 prenatally ascertained CCRs. Giardino D; Corti C; Ballarati L; Finelli P; Valtorta C; Botta G; Giudici M; Grosso E; Larizza L Prenat Diagn; 2006 Jun; 26(6):565-70. PubMed ID: 16683274 [TBL] [Abstract][Full Text] [Related]
56. A rare case of de novo distal 19q trisomy prenatally diagnosed. Rombout S; Sartenaer D; Parmentier B; Dugauquier C; Gillerot Y Prenat Diagn; 2004 Oct; 24(10):822-7. PubMed ID: 15503276 [TBL] [Abstract][Full Text] [Related]
57. Precise mapping of a de novo duplication 18(q21-->q22) utilizing cytogenetic, biochemical, and molecular techniques. Wolff DJ; Schwartz MF; Cohen MM; Schwartz S Am J Med Genet; 1993 Jun; 46(5):520-3. PubMed ID: 8322813 [TBL] [Abstract][Full Text] [Related]
58. Beckwith-Wiedemann syndrome due to 11p15.5 paternal duplication associated with Klinefelter syndrome and a "de novo" pericentric inversion of chromosome Y. Delicado A; Lapunzina P; Palomares M; Molina MA; Galán E; López Pajares I Eur J Med Genet; 2005; 48(2):159-66. PubMed ID: 16053907 [TBL] [Abstract][Full Text] [Related]
59. De novo inv del(4) in an infant with the Wolf-Hirschhorn syndrome. Serville F; Saura R; Billeaud C; Girard S; Choiset A; Longy M; Sandler B Ann Genet; 1987; 30(3):170-4. PubMed ID: 3499855 [TBL] [Abstract][Full Text] [Related]
60. Recombinant 4 syndrome due to an unbalanced pericentric inversion of chromosome 4. Battaglia A; Brothman AR; Carey JC Am J Med Genet; 2002 Sep; 112(1):103-6. PubMed ID: 12239731 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]