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PGD for dystrophin gene deletions using fluorescence in situ hybridization.
- Published in:
- Molecular Human Reproduction, 2006, v. 12, n. 5, p. 353, doi. 10.1093/molehr/gal039
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- Publication type:
- Article
Inherited mosaicism for the supernumerary marker chromosome in cat eye syndrome: Inter- and intra-individual variation and correlation to the phenotype.
- Published in:
- American Journal of Medical Genetics. Part A, 2012, v. 158A, n. 5, p. 1111, doi. 10.1002/ajmg.a.35311
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- Publication type:
- Article
Clinical outcome of treatment cycles using preimplantation genetic diagnosis for structural chromosomal abnormalities.
- Published in:
- 2001
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- Publication type:
- journal article
Highly abnormal cleavage divisions in preimplantation embryos from translocation carriers.
- Published in:
- Prenatal Diagnosis, 2000, v. 20, n. 13, p. 1038, doi. 10.1002/1097-0223(200012)20:13<1038::AID-PD976>3.0.CO;2-8
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- Publication type:
- Article
Swedish survey on extra structurally abnormal chromosomes in 39 105 consecutive prenatal diagnoses: prevalence and characterization by fluorescence in situ hybridization.
- Published in:
- 1994
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- Publication type:
- journal article
Trisomy 12 in HESC leads to no selective in vivo growth advantage in teratomas, but induces an increased abundance of renal development.
- Published in:
- Journal of Cellular Biochemistry, 2007, v. 100, n. 6, p. 1518, doi. 10.1002/jcb.21144
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- Publication type:
- Article
FISH-mapping of a 100-kb terminal 22q13 deletion.
- Published in:
- Human Genetics, 2002, v. 110, n. 5, p. 439, doi. 10.1007/s00439-002-0713-7
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- Publication type:
- Article
Fine mapping of the constitutional translocation t(11;22)(q23;q11).
- Published in:
- Human Genetics, 2000, v. 106, n. 5, p. 506, doi. 10.1007/s004390000287
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- Publication type:
- Article
An excess of chromosome 1 breakpoints in male infertility.
- Published in:
- European Journal of Human Genetics, 2004, v. 12, n. 12, p. 993, doi. 10.1038/sj.ejhg.5201263
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- Publication type:
- Article
Claes Lundsteen-in Memoriam.
- Published in:
- 2004
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- Publication type:
- Obituary
A comparison of different metaphase CGH methods for the detection of cryptic chromosome aberrations of defined size.
- Published in:
- European Journal of Human Genetics, 2004, v. 12, n. 6, p. 447, doi. 10.1038/sj.ejhg.5201175
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- Publication type:
- Article
Cryptic subtelomeric 6p deletion in a girl with congenital malformations and severe language impairment.
- Published in:
- European Journal of Human Genetics, 2003, v. 11, n. 1, p. 89, doi. 10.1038/sj.ejhg.5200907
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- Publication type:
- Article
Inv dup(22), del(22)(q11) and r(22) in the father of a child with DiGeorge syndrome.
- Published in:
- European Journal of Human Genetics, 2000, v. 8, n. 10, p. 801, doi. 10.1038/sj.ejhg.5200525
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- Publication type:
- Article
Origin of nondisjunction in trisomy 8 and trisomy 8 mosaicism.
- Published in:
- European Journal of Human Genetics, 1998, v. 6, n. 5, p. 432, doi. 10.1038/sj.ejhg.5200212
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- Publication type:
- Article
Spectral karyotyping and interphase FISH reveal abnormalities not detected by conventional G-banding.
- Published in:
- European Journal of Haematology, 2002, v. 68, n. 1, p. 31, doi. 10.1034/j.1600-0609.2002.00547.x
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- Publication type:
- Article
Identification of numerical and structural chromosome aberrations in 15 high hyperdiploid childhood acute lymphoblastic leukemias using spectral karyotyping.
- Published in:
- European Journal of Haematology, 2001, v. 66, n. 5, p. 297, doi. 10.1034/j.1600-0609.2001.066005297.x
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- Publication type:
- Article
Clonal culturing of human embryonic stem cells on laminin-521/E-cadherin matrix in defined and xeno-free environment.
- Published in:
- Nature Communications, 2014, v. 5, n. 1, p. 3195, doi. 10.1038/ncomms4195
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- Publication type:
- Article
Mechanical isolation of the inner cell mass is effective in derivation of new human embryonic stem cell lines.
- Published in:
- Human Reproduction, 2007, v. 22, n. 12, p. 3051
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- Publication type:
- Article
A culture system using human foreskin fibroblasts as feeder cells allows production of human embryonic stem cells.
- Published in:
- 2003
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- Publication type:
- journal article
Clinical and cytogenetic features of a population-based consecutive series of 285 pediatric T-cell acute lymphoblastic leukemias: Rare T-cell receptor gene rearrangements are associated with poor outcome.
- Published in:
- Genes, Chromosomes & Cancer, 2009, v. 48, n. 9, p. 795, doi. 10.1002/gcc.20684
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- Publication type:
- Article
Cytogenetic patterns in ETV6/RUNX1-positive pediatric B-cell precursor acute lymphoblastic leukemia: A Nordic series of 245 cases and review of the literature.
- Published in:
- Genes, Chromosomes & Cancer, 2007, v. 46, n. 5, p. 440, doi. 10.1002/gcc.20423
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- Publication type:
- Article
Spontaneously immortalized human T lymphocytes develop gain of chromosomal region 2p13–24 as an early and common genetic event.
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- Genes, Chromosomes & Cancer, 2004, v. 41, n. 2, p. 133, doi. 10.1002/gcc.20059
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- Publication type:
- Article
Amplification of the telomerase reverse transcriptase ( hTERT) gene in cervical carcinomas.
- Published in:
- Genes, Chromosomes & Cancer, 2002, v. 34, n. 3, p. 269, doi. 10.1002/gcc.10071
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- Publication type:
- Article
Severe phenotype of neurofibromatosis type 2 in a patient with a 7.4-MB constitutional deletion on chromosome 22: Possible localization of a neurofibromatosis type 2 modifier gene?
- Published in:
- Genes, Chromosomes & Cancer, 1999, v. 25, n. 2, p. 184, doi. 10.1002/(SICI)1098-2264(199906)25:2<184::AID-GCC15>3.0.CO;2-B
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- Publication type:
- Article
Interphase fluorescent in situ hybridization deletion analysis of the 9p21 region and prognosis in childhood acute lymphoblastic leukaemia (ALL): results from a prospective analysis of 519 Nordic patients treated according to the NOPHO-ALL 2000 protocol.
- Published in:
- British Journal of Haematology, 2011, v. 152, n. 5, p. 615, doi. 10.1111/j.1365-2141.2010.08532.x
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- Publication type:
- Article
Outcome of ETV6/RUNX1-positive childhood acute lymphoblastic leukaemia in the NOPHO-ALL-1992 protocol: frequent late relapses but good overall survival.
- Published in:
- British Journal of Haematology, 2008, v. 140, n. 6, p. 665, doi. 10.1111/j.1365-2141.2008.06980.x
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- Publication type:
- Article
Array-CGH reveals hidden gene dose changes in children with acute lymphoblastic leukaemia and a normal or failed karyotype by G-banding.
- Published in:
- British Journal of Haematology, 2008, v. 140, n. 5, p. 572, doi. 10.1111/j.1365-2141.2007.06917.x
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- Publication type:
- Article
Characterisation of dic(9;20)(p11–13;q11) in childhood B-cell precursor acute lymphoblastic leukaemia by tiling resolution array-based comparative genomic hybridisation reveals clustered breakpoints at 9p13.2 and 20q11.2.
- Published in:
- British Journal of Haematology, 2006, v. 135, n. 4, p. 492, doi. 10.1111/j.1365-2141.2006.06328.x
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- Publication type:
- Article
Cytogenetic abnormalities in childhood acute myeloid leukaemia: a Nordic series comprising all children enrolled in the NOPHO-93-AML trial between 1993 and 2001.
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- British Journal of Haematology, 2003, v. 121, n. 4, p. 566, doi. 10.1046/j.1365-2141.2003.04349.x
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- Publication type:
- Article
Interphase fluorescence in situ hybridization and spectral karyotyping reveals hidden genetic aberrations in children with acute lymphoblastic leukaemia and a normal banded karyotype.
- Published in:
- British Journal of Haematology, 2001, v. 114, n. 4, p. 786, doi. 10.1046/j.1365-2141.2001.03008.x
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- Publication type:
- Article
A full-coverage, high-resolution human chromosome 22 genomic microarray for clinical and research applications.
- Published in:
- Human Molecular Genetics, 2002, v. 11, n. 25, p. 3221, doi. 10.1093/hmg/11.25.3221
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- Publication type:
- Article
Molecular identification of a small supernumerary marker chromosome by in situ hybridization: diagnosis of an isochromosome 18p with probe L1.84.
- Published in:
- Clinical Genetics, 1991, v. 39, n. 6, p. 429, doi. 10.1111/j.1399-0004.1991.tb03054.x
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- Publication type:
- Article