[HTML][HTML] Monitoring of engraftment and progression of acute lymphoblastic leukemia in individual NOD/SCID mice
BA Nijmeijer, P Mollevanger… - Experimental …, 2001 - Elsevier
OBJECTIVE: The aim of this study was to develop an animal model for human acute
lymphoblastic leukemia (ALL) in which the kinetics and characteristics of leukemia can be …
lymphoblastic leukemia (ALL) in which the kinetics and characteristics of leukemia can be …
Ring chromosome 4 as the sole cytogenetic anomaly in a chondroblastoma: a case report and review of the literature
…, JVMG Bovée, HW Wessels, P Mollevanger… - Cancer genetics and …, 1998 - Elsevier
Chromosome analysis of a chondroblastoma of the right distal femur in a 31-year-old male
patient revealed a ring chromosome 4 in approximately one-third of the analyzed cells. The …
patient revealed a ring chromosome 4 in approximately one-third of the analyzed cells. The …
Proliferation and cytogenetic analysis of hairy cell leukemia upon stimulation via the CD40 antigen
HC Kluin-Nelemans, GC Beverstock, P Mollevanger… - 1994 - ashpublications.org
Using the CD40 system, in vitro proliferation of hairy cell leukemia (HCL) was examined in
43 patients. In this culture system, cells were stimulated by interleukin-4 (IL-4) and anti …
43 patients. In this culture system, cells were stimulated by interleukin-4 (IL-4) and anti …
Localization and polymorphism of a chromosome 12-specific α satellite DNA sequence
…, V Smit, JW Wessels, P Mollevanger… - … and Genome Research, 1990 - karger.com
The isolation and localization of a chromosome 12-specific α satellite DNA sequence,
pα12H8, is described. This clone contains a complete copy of the 1.4-kb Hin dlll higher …
pα12H8, is described. This clone contains a complete copy of the 1.4-kb Hin dlll higher …
Nasopharyngeal teratoma and mosaic tetrasomy 1q detected at amniocentesis: A case report and review of the literature
GC Beverstock, P Mollevanger, M Baaij, J Lind… - Cancer genetics and …, 1999 - Elsevier
The occurrence of nasopharyngeal teratomas (NPT) is an infrequent event and prenatal
detection of such tumors is even rarer. We present a case report and review of the literature …
detection of such tumors is even rarer. We present a case report and review of the literature …
Familial translocations involving 15q11-q13 can give rise to interstitial deletions causing Prader-Willi or Angelman syndrome.
…, K Buiting, C Lich, P Mollevanger… - Journal of medical …, 1996 - jmg.bmj.com
A de novo interstitial deletion of 15q11-q13 is the major cause of Prader-Willi syndrome
(PWS) and Angelman syndrome (AS). Here we describe two unrelated PWS patients with a …
(PWS) and Angelman syndrome (AS). Here we describe two unrelated PWS patients with a …
Pitt-Rogers-Danks syndrome and Wolf-Hirschhorn syndrome are caused by a deletion in the same region on chromosome 4p 16.3.
…, E Bakker, I Stec, D Donnai, P Mollevanger… - Journal of medical …, 1997 - jmg.bmj.com
Recently, a deletion of chromosome 4pter was found in three patients with Pitt-Rogers-
Danks syndrome. We investigated two of these patients, by means of DNA and FISH studies …
Danks syndrome. We investigated two of these patients, by means of DNA and FISH studies …
Premature menopause because of an inherited deletion in the long arm of the X-chromosome.
…, GC Beverstock, N Exalto, P Mollevanger - Fertility and …, 1991 - europepmc.org
Premature menopause because of an inherited deletion in the long arm of the X-chromosome. -
Abstract - Europe PMC Sign in | Create an account https://orcid.org Europe PMC Menu About …
Abstract - Europe PMC Sign in | Create an account https://orcid.org Europe PMC Menu About …
Generation and fluorescent in situ hybridization mapping of yeast artificial chromosomes of 1p, 17p, 17q, and 19q from a hybrid cell line by high-density screening of …
…, MC Wapenaar, EJ Meershoek, P Mollevanger… - Genomics, 1991 - Elsevier
A yeast artificial chromosome (YAC) library has been constructed from a somatic cell hybrid
containing at (1p; 19q) chromosome and chromosome 17. After amplification, part of this …
containing at (1p; 19q) chromosome and chromosome 17. After amplification, part of this …
Multiple supernumerary ring chromosomes of different origin in a patient: a clinical report and review of the literature
…, V Bezrookove, P Mollevanger… - American Journal of …, 2003 - Wiley Online Library
We describe a patient with multiple congenital abnormalities exhibiting 2–5 supernumerary
chromosomes per cells. A variety of FISH techniques were used to demonstrate that the …
chromosomes per cells. A variety of FISH techniques were used to demonstrate that the …