C. Lundsteen

发表

E. Granum, C. Lundsteen, T. Gerdes, 1981, Clinical genetics.

Automated multiple‐cell karyotyping: a clinical feasibility study

C. Lundsteen, T. Gerdes, J. Maahr, 1991, Clinical genetics.

Microphotometry of banded human chromosomes: High resolving power by direct scanning of the specimen compared with scanning on microphotographs

C. Lundsteen, J. Philip, 1974, Journal of medical genetics.

Human chromosome analysis by machine

J. Piper, C. Lundsteen, 1987 .

Automatic classification of chromosomes as part of a routine system for clinical analysis.

C Lundsteen, C. Lundsteen, T. Gerdes, 1986, Cytometry.

Detection of chromosomal gains and losses in comparative genomic hybridization analysis based on standard reference intervals.

C. Lundsteen, T. Gerdes, J. Maahr, 1998, Cytometry.

High resolution comparative genomic hybridisation in clinical cytogenetics

C. Lundsteen, M. Kirchhoff, H. Rose, 2001, Journal of medical genetics.

Disease associated balanced chromosome rearrangements: a resource for large scale genotype-phenotype delineation in man

Kim R. Rasmussen, C. Lundsteen, N. Tommerup, 2000, Journal of medical genetics.

Automated cytogenetic analysis: accomplishments, present status and practical future possibilities

C. Lundsteen, J. Philip, Claes Lundsteen, 1989, Clinical genetics.

Detection of chromosomal aberrations in seminomatous germ cell tumours using comparative genomic hybridization

C. Lundsteen, T. Gerdes, J. Philip, 1997, Genes, chromosomes & cancer.

Interstitial deletion of the short arm of chromosome 1: Attempt to establish a clinical phenotype (46,XX,del (1)(p22p32))

C. Lundsteen, M. Rethoré, C. Mircher, 2003, American journal of medical genetics. Part A.

Comparative genomic hybridization reveals non-random chromosomal aberrations in early preinvasive cervical lesions.

C. Lundsteen, T. Gerdes, J. Philip, 2001, Cancer genetics and cytogenetics.

Metaphase quality can be monitored by automatic counting of bands

C. Lundsteen, T. Gerdes, J. Maahr, 1994, Clinical genetics.

Comparison of cell cultures, chromosome quality and karyotypes obtained after chorionic villus sampling and early amniocentesis with filter technique

C. Lundsteen, J. Philip, K. Sundberg, 1999, Prenatal diagnosis.

Prenatal Diagnosis in Denmark

C. Lundsteen, L. Vejerslev, 1997, European journal of human genetics : EJHG.

Segmental haplosufficiency: transmitted deletions of 2p12 include a pancreatic regeneration gene cluster and have no apparent phenotypic consequences

J. Barber, C. Lundsteen, N. S. Thomas, 2005, European Journal of Human Genetics.

Non-disjunction of chromosome 13.

C. Lundsteen, N. Tommerup, H. Eiberg, 2007, Human molecular genetics.

Microphotometry of banded human chromosomes III

E. Granum, C. Lundsteen, 1976, Clinical genetics.

Comparative genomic hybridization in clinical cytogenetics.

C. Lundsteen, T. Gerdes, J. Philip, 1995, American journal of human genetics.

The selective miscarriage of Down's syndrome from 10 weeks of pregnancy

G. B. Petersen, C. Lundsteen, N. Wald, 1996, British journal of obstetrics and gynaecology.

De novo complex chromosomal rearrangements (CCR) involving chromosome 1, 5, and 6 resulting in microdeletion for 6q14 in a female carrier with psychotic disorder

C. Lundsteen, M. Kirchhoff, M. Rethoré, 2004, American journal of medical genetics. Part A.

A 5;7, 5;12 double reciprocal translocation in a normal mother and a 5;7 translocation with a recombinant chromosome 5 in her normal child.

C. Lundsteen, E. Niebuhr, A. Tabor, 1981, Journal of medical genetics.

The frequency of chromosome aberrations in tall men with special reference to 47, XYY and 47, XXY.

K. Hirschhorn, C. Lundsteen, J. Philip, 1976, American journal of human genetics.

Studies on the mechanism of chromosome banding with trypsin

C. Lundsteen, L. Kristoffersen, F. Ottosen, 2004, Humangenetik.

Randomised comparison of amniocentesis and transabdominal and transcervical chorionic villus sampling

C. Lundsteen, J. Philip, S. Fowler, 1992, The Lancet.

On the selection of systems for automated cytogenetic analysis.

C Lundsteen, C. Lundsteen, A O Martin, 1989, American journal of medical genetics.

Description of chromosome banding patterns by band transition sequences

E Granum, C Lundsteen, E. Granum, 1979, Clinical genetics.

High‐resolution comparative genomic hybridization detects extra chromosome arm 12p material in most cases of carcinoma in situ adjacent to overt germ cell tumors, but not before the invasive tumor development

H. Leffers, C. Lundsteen, N. Skakkebæk, 2003, Genes, chromosomes & cancer.

Erroneous Genetic Sex Determination of a Newborn Twin Girl due to Chimerism Caused by Foetal Blood Transfusion

C. Lundsteen, M. Schwartz, A. Byskov, 2003, Hormone Research in Paediatrics.

Aneuploidy as a marker for carcinoma-in-situ of the testis.

C. Lundsteen, N. Skakkeboek, J. Müller, 2009, Acta pathologica et microbiologica Scandinavica. Section A, Pathology.

Cytogenetic investigation of testicular carcinoma in situ and early seminoma by high-resolution comparative genomic hybridization analysis of subpopulations flow sorted according to DNA content.

N. Skakkebaek, C. Lundsteen, T. Gerdes, 2004, Cancer genetics and cytogenetics.

Cytogenetic and molecular analysis of a family with three brothers afflicted with germ‐cell cancer

C. Lundsteen, E. Rajpert-De Meyts, A. M. Ottesen, 2003, Clinical genetics.

Y-22 translocation in a YY male.

C. Lundsteen, J. Philip, 1973, Cytogenetics and cell genetics.

Transabdominal chorionic villus sampling in the second and third trimesters of pregnancy: Chromosome quality, reporting time, and feto‐maternal bleeding

C. Lundsteen, J. Philip, S. Smidt‐Jensen, 1993, Prenatal diagnosis.

An excess of chromosome 1 breakpoints in male infertility

R. Stallings, C. Lundsteen, Z. Tümer, 2004, European Journal of Human Genetics.

Randomised study of risk of fetal loss related to early amniocentesis versus chorionic villus sampling

C. Lundsteen, J. Philip, J. Parner, 1997, The Lancet.

The most common chromosome aberration detected by high-resolution comparative genomic hybridization in vulvar intraepithelial neoplasia is not seen in vulvar squamous cell carcinoma

C. Lundsteen, M. Kirchhoff, T. Bryndorf, 2004, Cytogenetic and Genome Research.

Balanced complex chromosomal rearrangements (BCCR) with at least three chromosomes and three or more breakpoints: report of three new cases.

C. Lundsteen, M. Rethoré, M. Bugge, 2004, Annales de genetique.

A complex four-break rearrangement between chromosomes 4 and 13 resulting in a recombinant chromosome 4.

C. Lundsteen, E. Niebuhr, O. Andersen, 1981, Cytogenetics and cell genetics.

Image analysis in comparative genomic hybridization.

P. Lichter, C. Lundsteen, T. Gerdes, 1995, Cytometry.

Choroideremia: further evidence for assignment of the locus to Xq13–Xq21

C. Lundsteen, E. Niebuhr, M. Schwartz, 1986, Human Genetics.

Comparative genomic hybridization reveals a recurrent pattern of chromosomal aberrations in severe dysplasia/carcinoma in situ of the cervix and in advanced‐stage cervical carcinoma

C. Lundsteen, T. Gerdes, J. Philip, 1999, Genes, chromosomes & cancer.

Further delineation of the 22q13 deletion syndrome

C. Lundsteen, N. Tommerup, M. Kirchhoff, 2005, Clinical dysmorphology.

High‐resolution comparative genomic hybridisation yields a high detection rate of chromosomal aberrations in childhood acute lymphoblastic leukaemia

C. Lundsteen, K. Schmiegelow, M. Kirchhoff, 2003, European journal of haematology.

Cytogenetic analysis of 2928 CVS samples and 1075 amniocenteses from randomized studies

C. Lundsteen, J. Philip, S. Smidt‐Jensen, 1993, Prenatal diagnosis.

Choroideremia in interstitial deletion of the X chromosome.

C. Lundsteen, T. Rosenberg, E. Niebuhr, 1986, Ophthalmic paediatrics and genetics.

Selective miscarriage of Down's syndrome fetuses in women aged 35 years and older

T. Chard, C. Lundsteen, C. Lundsteen, 1995, British journal of obstetrics and gynaecology.

Visual classification of banded human chromosomes. III. Classification and karyotyping of density profiles described by band transition sequences.

E. Granum, C. Lundsteen, 1979, Clinical genetics.

Automation of Cytogenetics

Jim Piper, Claes Lundsteen, J. Piper, 1989 .

Optimization of DOP-PCR amplification of DNA for high-resolution comparative genomic hybridization analysis.

H. Leffers, C. Lundsteen, J. Larsen, 2001, Cytometry.

Criminality in XYY and XXY men.

D B Rubin, K Hirschhorn, K O Christiansen, 1976, Science.

A familial, balanced 2-5 translocation associated with trisomy 21 in one individual.

C. Lundsteen, J. Philip, S. Vestermark, 1974, Human Heredity.

Microspectrophotometry of Trypsin-Leishman-stained Human Chromosomes

C. Lundsteen, J. Philip, P. Ernst, 1973, Nature.

Microphotometry of banded human chromosomes II:Technique for microphotography of banding patterns

C. Lundsteen, 1976, Clinical Genetics.

Prospective study comparing HR‐CGH and subtelomeric FISH for investigation of individuals with mental retardation and dysmorphic features and an update of a study using only HR‐CGH

C. Lundsteen, E. Kjeldsen, S. Kolvraa, 2004, American journal of medical genetics. Part A.

High resolution comparative genomic hybridisation analysis reveals imbalances in dyschromosomal patients with normal or apparently balanced conventional karyotypes

C. Lundsteen, T. Gerdes, Z. Tümer, 2000, European Journal of Human Genetics.

Systematic re-examination of carriers of balanced reciprocal translocations: a strategy to search for candidate regions for common and complex diseases

J. Hilden, C. Lundsteen, N. Tommerup, 2006, European Journal of Human Genetics.

Letters to the Editor

C. Lundsteen, 1976 .

[Chromosome aberrations in mentally retarded and dysmorphic patients with normal karyotypes].

C. Lundsteen, E. Kjeldsen, S. Kolvraa, 2004, Ugeskrift for laeger.

EARLY FILTRATION AMNIOCENTESIS FOR FURTHER INVESTIGATION OF MOSAICISM DIAGNOSED BY CHORIONIC VILLUS SAMPLING

C. Lundsteen, J. Philip, K. Sundberg, 1996, Prenatal diagnosis.

Randomized comparison of amniocentesis and transabdominal and transcervical chorionic villus sampling

C. Lundsteen, J. Philip, S. Fowler, 1993 .

[Randomized comparison of transabdominal, transcervical chorionic villi sampling and amniocentesis].

C. Lundsteen, J. Philip, S. Fowler, 1993, Ugeskrift for laeger.

Filtration and recirculation of early amniotic fluid. Evaluation of cell cultures from 100 diagnostic cases

C. Lundsteen, J. Philip, K. Sundberg, 1993, Prenatal diagnosis.

Biomonitoring of genotoxic exposure among stainless steel welders.

C. Lundsteen, L. Knudsen, J. Jelnes, 1992, Mutation research.

Cryptic familial t(11;18)(q25;q23) incidentally detected by interphase FISH

C. Lundsteen, T. Bryndorf, B. Christensen, 2001, Clinical genetics.

Visual classification of banded human chromosomes

Claes Lundsteen, Erik Granum, E. Granum, 1979 .

A test of a climate room for preparation of chromosome slides

C. Lundsteen, A. Lind, 1985, Clinical genetics.

Computer-assisted prenatal aneuploidy screening for chromosome 13, 18, 21, X and Y based on multiplex ligation-dependent probe amplification (MLPA)

C. Lundsteen, T. Gerdes, M. Schwartz, 2005, European Journal of Human Genetics.

Clinical performance of a system for semiautomated chromosome analysis.

C Lundsteen, C. Lundsteen, T. Gerdes, 1987, American journal of human genetics.

Semiautomated chromosome analysis: A clinical test

C Lundsteen, C. Lundsteen, J. Philip, 1985, Clinical genetics.

Microphotometry ofbanded humanchromosomes Highresolving power bydirect scanning ofthespecimen compared withscanning on microphotographs

C. Lundsteen, 1974 .

Automatic correction of the interfering effect of unsuppressed interspersed repetitive sequences in comparative genomic hybridization analysis.

C. Lundsteen, T. Gerdes, J. Maahr, 1997, Cytometry.

Interstitial deletion in the “critical region” of the long arm of the X chromosome in a mentally retarded boy and his normal mother

C. Lundsteen, E. Niebuhr, A. Tabor, 2004, Human Genetics.

Improved Sensitivity in Comparative Genomic Hybridization Analysis of DNA Heteroploid Cell Mixtures after Pre-Enrichment of Subpopulations by Fluorescence Activated Cell Sorting

C. Lundsteen, T. Gerdes, J. Larsen, 1999, Analytical Cellular Pathology.

High Resolution Comparative Genomic Hybridization Detects 7–8 Megabasepair Deletion in PCR Amplified DNA1

C. Lundsteen, J. Larsen, M. Kirchhoff, 2001, Analytical cellular pathology : the journal of the European Society for Analytical Cellular Pathology.

Deletions below 10 megabasepairs are detected in comparative genomic hybridization by standard reference intervals

C. Lundsteen, T. Gerdes, J. Maahr, 1999, Genes, chromosomes & cancer.

Prader‐Willi syndrome and chromosomal mosaicism 46, XY/47, XY, + mar in two cases

C. Lundsteen, F. Hansen, K. Michaelsen, 1979, Clinical genetics.

Comparative genomic hybridization reveals a recurrent pattern of chromosomal aberrations in severe dysplasia/carcinoma in situ of the cervix and in advanced-stage cervical carcinoma.

C. Lundsteen, T. Gerdes, J. Maahr, 1999, Genes, chromosomes & cancer.

Rapid prenatal diagnosis of trisomy 18 and triploidy in interphase nuclei of uncultured amniocytes by non‐radioactive in situ hybridization

C. Lundsteen, J. Philip, T. Bryndorf, 1992, Prenatal diagnosis.

Comparative genomic hybridization reveals a recurrent pattern of chromosomal aberrations in severe dysplasia/carcinoma in situ of the cervix and in advanced-stage cervical carcinoma.

C. Lundsteen, T. Gerdes, J. Maahr, 1999 .

Analysis of fluorescence ratio profiles in Comparative Genomic Hybridisation using statistical shape models.

J. Graham, C. Lundsteen, T. Gerdes, 2001 .

A 3.2 Mb deletion on 18q12 in a patient with childhood autism and high-grade myopia

G. Oliveira, A. Vicente, R. Cotterill, 2008, European Journal of Human Genetics.

Automatic chromosome analysis

E. Granum, B. Bjerregaard, C. Lundsteen, 1980, Clinical genetics.

INDICATION OF PRIMARY IMMUNE DEFICIENCY IN FANCONI'S ANEMIA

C. Lundsteen, M. Thomsen, F. K. Pedersen, 1977, Acta paediatrica Scandinavica.

Rapid prenatal diagnosis of chromosome aneuploidies by interphase fluorescence in situ hybridization: a one‐year clinical experience with high‐risk and urgent fetal and postnatal samples

C. Lundsteen, J. Philip, T. Bryndorf, 2000, Acta obstetricia et gynecologica Scandinavica.

rearrangements: a resource for large scale genotype-phenotype delineation in man

C. Lundsteen, N. Tommerup, E. Niebuhr, 2022 .