P. Mollevanger

Familial translocations involving 15q11-q13 can give rise to interstitial deletions causing Prader-Willi or Angelman syndrome.

Bernhard Horsthemke, Anneke Maat‐Kievit, Eva Sleegers et al. · Journal of Medical Genetics · 1996 · 82 citations · Full text

Interstitial Deletions, Genetics, Genetic Epidemiology +16

Premature menopause because of an inherited deletion in the long arm of the X-chromosome

Thiemo Veneman, Geoffrey C. Beverstock, N. Exalto et al. · Fertility and Sterility · 1991 · 78 citations

Infertility, Mendelian Disorder, Genetic Disorder +14

Localization and polymorphism of a chromosome 12-specific α satellite DNA sequence

Leendert H. J. Looijenga, Vincent T.H.B.M. Smit, J.W. Wessels et al. · Cytogenetic and Genome Research · 1990 · 73 citations

Proliferation and cytogenetic analysis of hairy cell leukemia upon stimulation via the CD40 antigen

Hanneke C. Kluin‐Nelemans, G.C. Beverstock, P. Mollevanger et al. · Blood · 1994 · 67 citations · Full text

Monitoring of engraftment and progression of acute lymphoblastic leukemia in individual NOD/SCID mice

Bart Nijmeijer, P. Mollevanger, Shama L. van Zelderen‐Bhola et al. · Experimental Hematology · 2001 · 49 citations · Full text

Hematological Malignancy, Cell Therapy, Stem Cell Transplantation +8