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

Bernhard Horsthemke, Anneke Maat‐Kievit, Eva Sleegers, +7

Journal of Medical Genetics

Interstitial DeletionsGeneticsGenetic EpidemiologyPathologyDisease Gene Identification +14

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

Thiemo Veneman, Geoffrey C. Beverstock, N. Exalto, +1

Fertility and Sterility

InfertilityMendelian DisorderGenetic DisorderGeneticsLong Arm +12

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, +4

Cytogenetic and Genome Research

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

Hanneke C. Kluin‐Nelemans, G.C. Beverstock, P. Mollevanger, +4

Blood

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

Bart Nijmeijer, P. Mollevanger, Shama L. van Zelderen‐Bhola, +3

Experimental Hematology

Hematological MalignancyCell TherapyStem Cell TransplantationImmunologyHematology +6

Pitt-Rogers-Danks syndrome and Wolf-Hirschhorn syndrome are caused by a deletion in the same region on chromosome 4p 16.3.

Sarina G. Kant, Arie van Haeringen, E Bakker, +6

Journal of Medical Genetics

ChromatinWolf-hirschhorn SyndromeMendelian DisorderCytogeneticsGenetic Disorder +13

Combined GTG-banding and nonradioactive in situ hybridization improves characterization of complex karyotypes

Vincent T.H.B.M. Smit, J.W. Wessels, P. Mollevanger, +4

Cytogenetic and Genome Research

CytogeneticsGeneticsMolecular BiologyGynecologyMolecular Genetics +18

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 an amplified library

M. Driesen, Johannes G. Dauwerse, Martin C. Wapenaar, +5

Genomics

ChromatinSitu Hybridization MappingMolecular Biological MethodHybridizationGenetics +8

Improved interpretation of complex chromosomal rearrangements by combined GTG banding and in situ suppression hybridization using chromosome‐specific libraries and cosmid probes

Vincent T.H.B.M. Smit, J.W. Wessels, P. Mollevanger, +7

Genes Chromosomes and Cancer

Two distinct loci on the short arm of chromosome 16 are involved in myeloid leukemia

J. Wessels, P. Mollevanger, JG Dauwerse, +3

Blood