Detalhe da pesquisa
1.
One-cell biopsy significantly improves the outcome of preimplantation genetic diagnosis (PGD) treatment: retrospective analysis of 569 PGD cycles at the Stockholm PGD centre.
Hum Reprod
; 27(9): 2843-9, 2012 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-22736325
2.
Improved structural characterization of chromosomal breakpoints using high resolution custom array-CGH.
Clin Genet
; 77(6): 552-62, 2010 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-20236111
3.
Detailed molecular and clinical characterization of three patients with 21q deletions.
Clin Genet
; 77(2): 145-54, 2010 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-19863549
4.
Concurrent microdeletion and duplication of 22q11.2.
Clin Genet
; 74(1): 61-7, 2008 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-18445048
5.
Frequent amplification of the telomerase reverse transcriptase gene in human tumors.
Cancer Res
; 60(22): 6230-5, 2000 Nov 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-11103775
6.
Inv dup(22), del(22)(q11) and r(22) in the father of a child with DiGeorge syndrome.
Eur J Hum Genet
; 8(10): 801-4, 2000 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-11039583
7.
Tetrasomy 18p de novo: parental origin and different mechanisms of formation.
Eur J Hum Genet
; 4(3): 160-7, 1996.
Artigo
em Inglês
| MEDLINE | ID: mdl-8840116
8.
Origin of nondisjunction in trisomy 8 and trisomy 8 mosaicism.
Eur J Hum Genet
; 6(5): 432-8, 1998.
Artigo
em Inglês
| MEDLINE | ID: mdl-9801867
9.
Maternal isodisomy of chromosome 9 with no impact on the phenotype in a woman with two isochromosomes: i(9p) and i(9q).
Am J Med Genet
; 87(1): 49-52, 1999 Nov 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-10528247
10.
Monosomy 1p36.31-33-->pter due to a paternal reciprocal translocation: prognostic significance of FISH analysis.
Am J Med Genet
; 65(1): 60-7, 1996 Oct 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-8914743
11.
Trisomy 5q12-->q13.3 in a patient with add(13q): characterization of an interchromosomal insertion by forward and reverse chromosome painting.
Am J Med Genet
; 73(3): 351-5, 1997 Dec 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-9415698
12.
Fifty probands with extra structurally abnormal chromosomes characterized by fluorescence in situ hybridization.
Am J Med Genet
; 55(1): 85-94, 1995 Jan 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-7702104
13.
Molecular cytogenetic characterization and origin of two de novo duplication 9p cases.
Am J Med Genet
; 91(2): 102-6, 2000 Mar 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-10748406
14.
Detailed characterization of 12 supernumerary ring chromosomes using micro-FISH and search for uniparental disomy.
Am J Med Genet
; 99(3): 223-33, 2001 Mar 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-11241494
15.
Detailed characterization of a complex karyotype in a patient with primary plasma cell leukaemia using multicolour spectral karyotyping and micro-FISH.
Hematol J
; 1(2): 95-101, 2000.
Artigo
em Inglês
| MEDLINE | ID: mdl-11920176
16.
Physical state of HPV16 and chromosomal mapping of the integrated form in cervical carcinomas.
Diagn Mol Pathol
; 10(1): 46-54, 2001 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-11277395
17.
A case of acute lymphoblastic leukemia, near-triploidy, and poor outcome: characterization by fluorescence in situ hybridization using chromosome-specific libraries from all human chromosomes.
Cancer Genet Cytogenet
; 99(2): 93-6, 1997 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-9398861
18.
DNA image analysis in childhood acute lymphoblastic leukemia.
Leuk Lymphoma
; 9(3): 229-35, 1993 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-8471982
19.
New chromosomal breakpoints in non-Hodgkin's lymphomas revealed by spectral karyotyping and G-banding.
Int J Mol Med
; 5(5): 485-92, 2000 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-10762651
20.
Generation of dendritic cells from peripheral blood of patients at different stages of chronic myeloid leukemia.
Med Oncol
; 17(4): 270-8, 2000 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-11114705