Maternal uniparental heterodisomy of chromosome 14: chromosomal mechanism and clinical follow up
Sanlaville, D, Aubry, M C, Dumez, Y, Nolen, M C, Amiel, J, Pinson, M P, Lyonnet, S, Munnich, A, Vekemans, M, Morichon-Delvallez, N
Published in Journal of medical genetics (01.07.2000)
Published in Journal of medical genetics (01.07.2000)
Get full text
Journal Article
Pure trisomy 20p resulting from isochromosome formation and whole arm translocation
SIDWELL, R U, PINSON, M-P, GIBBONS, B, BYATT, S-A, SVENNEVIK, E C, HASTINGS, R J, FLYNN, D M
Published in Journal of medical genetics (01.06.2000)
Published in Journal of medical genetics (01.06.2000)
Get full text
Journal Article
Prenatal detection of a 1p36 deletion in a fetus with multiple malformations and a review of the literature
Faivre, L., Morichon-Delvallez, N., Viot, G., Martinovic, J., Pinson, M. P., Aubry, J. P., Raclin, V., Edery, P., Dumez, Y., Munnich, A., Vekemans, M.
Published in Prenatal diagnosis (01.01.1999)
Published in Prenatal diagnosis (01.01.1999)
Get full text
Journal Article
Prenatal diagnosis of a satellited non-acrocentric chromosome derived from a maternal translocation (10;13)(p13;p12) and review of literature
Faivre, L., Morichon-Delvallez, N., Viot, G., Larget-Piet, A., Narcy, F., Turleau, C., Pinson, M. P., Dumez, Y., Munnich, A., Vekemans, M.
Published in Prenatal diagnosis (01.03.1999)
Published in Prenatal diagnosis (01.03.1999)
Get full text
Journal Article
Sequential FISH reveals an abnormal karyotype involving 14 chromosomes in a child with acute lymphoblastic leukemia
Pinson, M P, Martineau, M, Jabbar, M S, Kilby, A M, Walker, H, Harrison, C J
Published in Leukemia (01.09.2000)
Published in Leukemia (01.09.2000)
Get full text
Journal Article