Charcot's links with Britain. Don't rely on Munthe's autobiography.

অনুযায়ী Bonduelle, M.
প্রকাশিত 1994

A comparative study of danazol and norethisterone in dysfunctional uterine bleeding presenting as menorrhagia.

অনুযায়ী Bonduelle, M., Walker, J. J., Calder, A. A.
প্রকাশিত 1991

High frequency of BRCA1/2 germline mutations in 42 Belgian families with a small number of symptomatic subjects

অনুযায়ী Goelen, G, Teugels, E, Bonduelle, M, Neyns, B, De Greve, J
প্রকাশিত 1999

Metabolic Syndrome and Its Components in Young Adults Conceived by ICSI

অনুযায়ী Belva, F., Bonduelle, M., Provyn, S., Painter, R. C., Tournaye, H., Roelants, M., De Schepper, J.
প্রকাশিত Int J Endocrinol (2018)

Mild pulmonary, but severe hepatic disease in a cystic fibrosis patient homozygous for a frameshift mutation in the regulatory domain of the CFTR.

অনুযায়ী Lissens, W, Desmyttere, S, Bonduelle, M, Dab, I, Liebaers, I, Mercier, B, Audrezet, M P, Ferec, C
প্রকাশিত 1993

Is congenital bilateral absence of vas deferens a primary form of cystic fibrosis? Analyses of the CFTR gene in 67 patients.

অনুযায়ী Mercier, B, Verlingue, C, Lissens, W, Silber, S J, Novelli, G, Bonduelle, M, Audrézet, M P, Férec, C
প্রকাশিত 1995

The impact of proband mediated information dissemination in families with a BRCA1/2 gene mutation

অনুযায়ী Sermijn, E, Goelen, G, Teugels, E, Kaufman, L, Bonduelle, M, Neyns, B, Poppe, B, De Paepe, A, De Greve, J
প্রকাশিত 2004

Body composition and blood pressure in 6-year-old singletons born after pre-implantation genetic testing for monogenic and structural chromosomal aberrations: a matched cohort stud...

অনুযায়ী Belva, F, Roelants, M, Kluijfhout, S, Winter, C, De Schrijver, F, Desmyttere, S, De Rycke, M, Tournaye, H, Liebaers, I, Bonduelle, M
প্রকাশিত Hum Reprod Open (2018)

Chromosome 13q deletion with Waardenburg syndrome: further evidence for a gene involved in neural crest function on 13q.

অনুযায়ী Van Camp, G, Van Thienen, M N, Handig, I, Van Roy, B, Rao, V S, Milunsky, A, Read, A P, Baldwin, C T, Farrer, L A, Bonduelle, M
প্রকাশিত 1995

Localisation of the gene causing diaphyseal dysplasia Camurati-Engelmann to chromosome 19q13

অনুযায়ী Janssens, K., Gershoni-Baruch, R., Van Hul, E., Brik, R., Guanabens, N., Migone, N., Verbruggen, L., Ralston, S., Bonduelle, M., Van Maldergem, L., Vanhoenacker, F., Van Hul, W.
প্রকাশিত 2000

Camurati‐Engelmann disease: review of the clinical, radiological, and molecular data of 24 families and implications for diagnosis and treatment

অনুযায়ী Janssens, K, Vanhoenacker, F, Bonduelle, M, Verbruggen, L, Van Maldergem, L, Ralston, S, Guañabens, N, Migone, N, Wientroub, S, Divizia, M T, Bergmann, C, Bennett, C, Simsek, S, Melançon, S, Cundy, T, Van Hul, W
প্রকাশিত 2006

A high proportion of novel mutations in BRCA1 with strong founder effects among Dutch and Belgian hereditary breast and ovarian cancer families

অনুযায়ী Peelen, T., van Vliet, M., Petrij-Bosch, A., Mieremet, R., Szabo, C., van den Ouweland, A. M. W., Hogervorst, F., Brohet, R., Ligtenberg, M. J. L., Teugels, E., van der Luijt, R., van der Hout, A. H., Gille, J. J. P., Pals, G., Jedema, I., Olmer, R., van Leeuwen, I., Newman, B., Plandsoen, M., van der Est, M., Brink, G., Hageman, S., Arts, P. J. W., Bakker, M. M., Willems, H. W., van der Looij, E., Neyns, B., Bonduelle, M., Jansen, R., Oosterwijk, J. C., Sijmons, R., Smeets, H. J. M., van Asperen, C. J., Meijers-Heijboer, H., Klijn, J. G. M., de Greve, J., King, M.-C., Menko, F. H., Brunner, H. G., Halley, D., van Ommen, G.-J. B., Vasen, H. F. A., Cornelisse, C. J., van 'tVeer, L. J., de Knijff, P., Bakker, E., Devilee, P.
প্রকাশিত 1997