Tumor-specific loss of 11p15.5 alleles in del11p13 Wilms tumor and in familial adrenocortical carcinoma.

Isabelle Henry, S Grandjouan, P. Couillin, +6

Proceedings of the National Academy of Sciences

Malformation SyndromesGeneticsPathologyMolecular GeneticsDisease Gene Identification +18

Molecular definition of the 11p15.5 region involved in Beckwith-Wiedemann syndrome and probably in predisposition to adrenocortical carcinoma

Isabelle Henry, Marc Jeanpierre, P. Couillin, +7

Human Genetics

Beckwith-wiedemann SyndromeAdrenocortical CarcinomaPathologyAdrenal DiseaseDermatology +3

Molecular definition of de novo and genetically transmitted WAGR-associated rearrangements of 11p13

Christian Lavedan, F. Barichard, M Azoulay, +7

Cytogenetic and Genome Research

CytogeneticsGeneticsGenomic MechanismMolecular BiologyPathology +15

Mapping of a human fibrillar collagen gene, pro α1(XI) (COL11A1), to the p21 region of chromosome 1

Isabelle Henry, Alain Bernheim, Michael P. Bernard, +7

Genomics

ChromatinChromosome DynamicsFibrosisCytogeneticsGenetics +10

Characterization of a panel of somatic cell hybrids for subregional mapping along 11p and within band 11p13

P. Couillin, M Azoulay, Isabelle Henry, +8

Human Genetics

Cell DivisionSomatic Cell GeneticsMedicineSubregional MappingMolecular Biology +6

Chromosomal assignment of the human 2,3-bisphosphoglycerate mutase gene (BPGM) to region 7q34→7q22

F. Barichard, V. Joulin, Isabelle Henry, +5

Human Genetics

Developmental BiologyChromosomal AssignmentCytogeneticsGenetic DisorderGenetics +7

The isolation, characterisation, and chromosomal assignment of the gene for human 3-hydroxy-3-methylglutaryl coenzyme A reductase, (HMG-CoA reductase)

Steve E. Humphries, F. Tata, Isabelle Henry, +4

Human Genetics

ChromatinChromosomal AssignmentBiochemistryCytogeneticsHmg-coa Reductase +8

Duplication of HRAS1, INS, and IGF2 is not a common event in Beckwith-Wiedemann syndrome.

Isabelle Henry, Marc Jeanpierre, F. Barichard, +5

PubMed

Single base pair germ-line deletion in the p53 gene in a cancer predisposed family

Richard C. Hamelin, F. Barichard, Isabelle Henry, +2

Human Genetics

Genome InstabilityP53 GeneGeneticsMolecular GeneticsTumor Suppressor +5

Pericentric intrachromosomal insertion responsible for recurrence of del(11)(p13p14) in a family

Isabelle Henry, J.M.N. Hoovers, F. Barichard, +7

Genes Chromosomes and Cancer