P. Jensen

发表

A 5p;22q reciprocal translocation with a high risk for segregation of unbalanced offspring

P. Jensen, 1984 .

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.

An excess of chromosome 1 breakpoints in male infertility

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

Application of fluorescence in situ hybridization techniques in clinical genetics: use of two alphoid repeat probes detecting the centromeres of chromosomes 13 and 21 or chromosomes 14 and 22, respectively

K. B. Petersen, L. Bolund, S. Kolvraa, 1991, Clinical genetics.

Prenatal diagnosis of a 46,XX/47,XX, +12 mosaic

H. Rehder, E. Schwinger, U. Friedrich, 1984, Prenatal diagnosis.

Molecular cytogenetic detection of 9q34 breakpoints associated with nail patella syndrome

E. Mariman, A. Silahtaroglu, Z. Tümer, 1999, European Journal of Human Genetics.

Novel Mutations Including Deletions of the Entire OFD1 Gene in 30 Families with Type 1 Orofaciodigital Syndrome: A Study of the Extensive Clinical Variability

D. Horn, K. Heimdal, D. Wieczorek, 2013, Human mutation.

A biastellited marker chromosome in an infant with the caudal regression anomalad

P. Hansen, P. Jensen, 1981, Clinical genetics.

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.

Transabdominal chorionic villi sampling for first trimester fetal diagnosis. First 26 pregnancies followed to term

S. Smidt‐Jensen, J. Hariri, P. Jensen, 1986 .

Experience with transabdominal fine needle biopsy from chorionic villi in the first trimester: an alternative to amniocentesis

S. Smidt‐Jensen, N. Hahnemann, P. Jensen, 1984 .

The molecular diagnosis of spinocerebellar ataxia type 1 in patients with ataxia

K. Fenger, S. Sørensen, J. Nielsen, 1997 .

Limited use of chromosomal markers in prenatal diagnosis

U. Friedrich, P. Jensen, 1983, Prenatal Diagnosis.

Four cases of the prenatal diagnosis of trisomy 20 mosaicism with a follow up investigation

G. Bruun-Petersen, U. Friedrich, P. Jensen, 1984 .

Prenatal cytogenetic diagnosis after transabdominal chorionic villus sampling in the first trimester

J. Hertz, S. Smidt‐Jensen, N. Hahnemann, 1988, Prenatal diagnosis.

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

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