M. Breuning

发表

Inversion 16 and translocation (16;16) in ANLL M4eo break in the same subregion of the short arm of chromosome 16.

G. Beverstock, H. Wessels, H. Dauwerse, 1991, Cancer genetics and cytogenetics.

Differentiation induction in acute promyelocytic leukemia

G. Rector, J. .. Bemmel, M. Breuning, 2011 .

Extending the phenotype of recurrent rearrangements of 16p11.2: deletions in mentally retarded patients without autism and in normal individuals.

J. Schuurs-Hoeijmakers, R. Pfundt, P. Lapunzina, 2009, European journal of medical genetics.

The NDE1 gene is disrupted by the inv(16) in 90% of cases with CBFB–MYH11-positive acute myeloid leukemia

J. Jansen, A. Simons, M. Massop, 2010, Leukemia.

A murine model for juvenile NCL: gene targeting of mouse Cln3.

R. Nussbaum, N. Greene, N. de Vos, 1999, Molecular genetics and metabolism.

Hereditary leiomyomatosis and renal cell cancer in families referred for fumarate hydratase germline mutation analysis

L. Hoefsloot, S. Shanley, M. Breuning, 2011, Clinical genetics.

Duchenne/Becker muscular dystrophy in the family: have potential carriers been tested at a molecular level?

J. Verschuuren, A. Tibben, M. Breuning, 2011, Clinical genetics.

Germline mutations in APC and MUTYH are responsible for the majority of families with attenuated familial adenomatous polyposis

H. Morreau, M. Weiss, M. Breuning, 2007, Clinical genetics.

An unanticipated copy number variant of chromosome 15 disrupting SMAD3 reveals a three‐generation family at serious risk for aortic dissection

G. Pals, M. Reijnierse, A. Haeringen, 2013, Clinical genetics.

Spectrum of mutations in the Batten disease gene, CLN3.

T. Lerner, P. Munroe, P. Taschner, 1997, American journal of human genetics.

Batten disease gene, CLN3: linkage disequilibrium mapping in the Finnish population, and analysis of European haplotypes.

I. Järvelä, S. Mole, H. Mitchison, 1995, American journal of human genetics.

Genomic structure and complete nucleotide sequence of the Batten disease gene, CLN3.

R. Moyzis, A. C. Munk, N. de Vos, 1997, Genomics.

Two step procedure for early diagnosis of polycystic kidney disease with polymorphic DNA markers on both sides of the gene.

P. Pearson, E. Bakker, J. Saris, 1990, Journal of medical genetics.

Recurrence risk due to germ line mosaicism: Duchenne and Becker muscular dystrophy

J. Houwing-Duistermaat, J. D. den Dunnen, E. Bakker, 2009, Clinical genetics.

Detection of CBP rearrangements in acute myelogenous leukemia with t(8;16)

H. Döhner, A. Hagemeijer, G. V. Ommen, 1997, Leukemia.

A Dutch MYH7 founder mutation, p.(Asn1918Lys), is associated with early onset cardiomyopathy and congenital heart defects

D. Barge-Schaapveld, C. Ruivenkamp, R. L. Lekanne Deprez, 2017, Netherlands Heart Journal.

Gene defect in polycystic kidney disease.

M. Breuning, 1995, Experimental nephrology.

Invasive prenatal diagnosis after intracytoplasmic sperm injection.

L. V. D. van der Westerlaken, F. Helmerhorst, N. Naaktgeboren, 2001, Fertility and Sterility.

Rapid detection of the major deletion in the Batten disease gene CLN3 by allele specific PCR.

P. Taschner, M. Breuning, N. de Vos, 1997, Journal of medical genetics.

Extensive cross-homology between the long and the short arm of chromosome 16 may explain leukemic inversions and translocations.

A. Hagemeijer, J. Saris, M. Breuning, 1992, Blood.

Rapid detection of chromosome 16 inversion in acute nonlymphocytic leukemia, subtype M4: regional localization of the breakpoint in 16p.

A. Hagemeijer, P. Pearson, M. Breuning, 1990, Cytogenetics and cell genetics.

X‐chromosome duplications in males with mental retardation: pathogenic or benign variants?

E. Bakker, C. Ruivenkamp, A. van Haeringen, 2011, Clinical genetics.

Natural H-2-specific antibodies in sera of aged mice

A. Kruisbeek, M. Breuning, P. Mourik, 2004, Immunogenetics.

X‐chromosome duplications in males with mental retardation: pathogenic or benign variants?

E. Bakker, C. Ruivenkamp, A. van Haeringen, 2011, Clinical genetics.