Novel Types of Mutation Responsible for the Dermatosparactic Type of Ehlers–Danlos Syndrome (Type VIIC) and Common Polymorphisms in the ADAMTS2 Gene

Alain Colige, Lieve Nuytinck, Anthonie J. van Essen, +11

Journal of Investigative Dermatology

Mendelian DisorderGenetic DisorderGeneticsPathogenesisGenetic Epidemiology +9

Submicroscopic terminal deletions and duplications in retarded patients with unclassified malformation syndromes

Mariluce Riegel, Alessandra Baumer, Mauricette Jamar, +4

Human Genetics

Developmental AnomalyPediatricsPathologySubmicroscopic Terminal DeletionsUnclassified Malformation Syndromes +1

Leukemia : Official Journal of the Leukemia Society of America, Leukemia Research Fund, U.K

Isabelle Luquet, Jia‐Qi Lai, Carole Barin, +25

Leukemia SocietyHematological MalignancyMedicineMixed-phenotype Acute LeukemiaHematology +7

Identification of cytogenetic subclasses and recurring chromosomal aberrations in AML and MDS with complex karyotypes using m‐FISH

Heidi Van Limbergen, Bruce Poppe, Lucienne Michaux, +7

Genes Chromosomes and Cancer

High Frequency of JAZF1-JJAZ1 Gene Fusion in Endometrial Stromal Tumors With Smooth Muscle Differentiation by Interphase FISH Detection

Esther Oliva, Laurence de Leval, Robert A. Soslow, +1

The American Journal of Surgical Pathology

ChromatinTumoral PathologySmooth Muscle DifferentiationJazf1-jjaz1 Gene FusionMedicine +9

Major decrease in the incidence of trisomy 21 at birth in south Belgium: mass impact of triple test?

Alain Verloès, Y. Gillerot, Lionel Van Maldergem, +6

European Journal of Human Genetics

Down SyndromeFertilityReproductive HealthPediatricsGenetic Epidemiology +11

<i>PAX5/IGH</i> rearrangement is a recurrent finding in a subset of aggressive B‐NHL with complex chromosomal rearrangements

Bruce Poppe, Pascale De Paepe, Lucienne Michaux, +12

Genes Chromosomes and Cancer

MLL amplification in myeloid leukemias: A study of 14 cases with multiple copies of 11q23

Lucienne Michaux, Iwona Włodarska, Michel Stul, +17

Genes Chromosomes and Cancer

Elderly PatientsCytogeneticsMixed-phenotype Acute LeukemiaPathologyTumor Biology +14

<i>PRDM16</i> (1p36) translocations define a distinct entity of myeloid malignancies with poor prognosis but may also occur in lymphoid malignancies

François P. Duhoux, Geneviève Ameye, Carmen P. Montano‐Almendras, +24

British Journal of Haematology

Improved detection of chromosomal abnormalities in chronic lymphocytic leukemia by conventional cytogenetics using CpG oligonucleotide and interleukin‐2 stimulation: A Belgian multicentric study

Natalie Put, Peter Könings, Katrina Rack, +13

Genes Chromosomes and Cancer