H. Müller

发表

Novel germline APC gene mutation in a large familial adenomatous polyposis kindred displaying variable phenotypes.

R. Scott, R. B. van der Luijt, J. Mary, 1995, Gut.

Germline alterations in the cyclooxygenase‐2 gene are not associated with the development of extracolonic manifestations in a large Swiss familial adenomatous polyposis kindred

H. Müller, Z. Dobbie, I. Bendik, 2000, International journal of cancer.

Detection of new mutations in six out of 10 Swiss HNPCC families by genomic sequencing of the hMSH2 and hMLH1 genes.

R. Scott, J. Buerstedde, J. Torhorst, 1995, Journal of medical genetics.

Mutational analysis of the first 14 exons of the adenomatous polyposis coli (APC) gene.

R. Scott, R. Ammann, T. Ammann, 1994, European journal of cancer.

Induction and removal of interstrand crosslinks in the ribosomal RNA genes of lymphoblastoid cell lines from patients with Fanconi anemia.

R. Scott, H. Müller, Jean-Philippe Rey, 1993, Mutation research.

BRCA1 mutations in a selected series of breast/ovarian cancer patients.

R. Scott, R. Herrmann, J. Torhorst, 1996, Journal of medical genetics.

Association of Extracolonic Manifestations of Familial Adenomatous Polyposis with Acetylation Phenotype in a Large FAP Kindred

R. Scott, U. Meyer, K. Heinimann, 1997, European journal of human genetics : EJHG.

A polymorphism in the ATM gene modulates the penetrance of hereditary non‐polyposis colorectal cancer

P. Chappuis, P. Hutter, A. Sappino, 2000, International journal of cancer.

Immunochemical determination of an initial step in thymine dimer excision repair in xeroderma pigmentosum variant fibroblasts and biopsy material from the normal population and patients with basal cell carcinoma and melanoma.

J. Boyle, H. Müller, M. Roth, 1987, Carcinogenesis.

Germline mutations in the β-catenin gene are not associated with the FAP phenotype without an APC mutation

H. Müller, Z. Dobbie, 1999, Journal of medical genetics.

Variations in karyotypes of normal premature babies, new-born babies and infants

H. Müller, 2004, Humangenetik.

Silver staining of nucleolus organizer regions during human spermatogenesis

M. Schmid, W. Engel, H. Müller, 2004, Human Genetics.

Chromosomes and human neoplasms

G. Stalder, H. Müller, 1976, European Journal of Pediatrics.

[Identification and genetic counseling of people with HNPCC (hereditary nonpolyposis colorectal cancer): old and new research goals].

K. Heinimann, H. Müller, Z. Dobbie, 1999, Schweizerische medizinische Wochenschrift.

Correlation between the development of extracolonic manifestations in FAP patients and mutations beyond codon 1403 in the APC gene.

R. Scott, J. Mary, M. Spycher, 1996, Journal of medical genetics.

Distamycin A/DAPI staining of heterochromatin in male meiosis of man

M. Schmid, T. Haaf, H. Müller, 1986, Genetica.

Immunochemical determination of thymine dimer repair in xeroderma pigmentosum variant fibroblasts and biopsy material from the normal population and patients with basal cell carcinom and melanoma

J. Boyle, H. Müller, M. Roth, 1988 .

Chromosome polymorphism in a human newborn population

H. Klinger, H. Müller, M. Glasser, 1975 .

Chromosome polymorphism in a human newborn population. II. Potentials of polymorphic chromosome variants for characterizing the idiogram of an individual.

H. Klinger, H. Müller, M. Glasser, 1975, Cytogenetics and cell genetics.

Nontruncating APC germ-line mutations and mismatch repair deficiency play a minor role in APC mutation-negative polyposis.

G. Marra, K. Heinimann, D. Foernzler, 2001, Cancer research.

Trisomy-18 syndrome caused by translocation or isochromosome formation. A case report with bibliography.

E. Signer, G. Stalder, H. Müller, 1972, Journal of medical genetics.

New Methods to Detect Sulfur Mustard (SM) and SM-Induced Skin Damage

K. Kehe, H. Müller, H. Thiermann, 2009 .

Thymine dimer repair in fibroblasts of patients with dysplastic naevus syndrome (DNS)

J. Boyle, H. Müller, M. Roth, 1988, Experientia.

Microsatellite instability in colorectal cancer.

K. Heinimann, H. Müller, Z. Dobbie, 2000, The New England journal of medicine.

Trisomy-18 syndrome caused by translocation or isochromosome formation. A case report with bibliography.

E. Signer, G. Stalder, H. Müller, 1972, Journal of Medical Genetics.