Halliger-Keller, B: search on Z-Library

The world's largest scientific articles store. 70,000,000+ articles for free.

Don't use scam websites

1

The genetic defect of the alkaptonuric mouse (aku)

W. Kress, S.R. Schmidt, B. Halliger-Keller, X. Montagutelli, C.R. Müller

Journal:

Mammalian Genome

Year:

1999

Language:

english

File:

PDF, 296 KB

english, 1999

2

CCM1gene deletion identified by MLPA in cerebral cavernous malformation

Sabine Gaetzner, Sonja Stahl, Oguzkan Sürücü, Anne Schaafhausen, Birgit Halliger-Keller, Helmut Bertalanffy, Ulrich Sure, Ute Felbor

Journal:

Neurosurgical Review

Year:

2007

Language:

english

File:

PDF, 330 KB

english, 2007

3

Allelic heterogeneity of alkaptonuria in Central Europe

Müller, C R, Fregin, A, Srsen, S, Srsnova, K, Halliger-Keller, B, Felbor, U, Seemanova, E, Kress, W

Journal:

European Journal of Human Genetics

Year:

1999

Language:

english

File:

PDF, 213 KB

english, 1999

4

Genetic heterogeneity of oculopharyngeal muscular dystrophy (OPMD)

C.R. Müller, W. Kress, H. Porschke, B. Halliger-Keller, T. Grimm

Journal:

Neuromuscular Disorders

Year:

1996

Language:

english

File:

PDF, 118 KB

english, 1996

5

No evidence for heterogeneity in oculopharyngeal muscular dystrophy.

Kress, W, Halliger-Keller, B, Grimm, T, Porschke, H, Engelhardt, A, Goebel, H H, Muller-Mysok, B

Journal:

Journal of Medical Genetics

Year:

1998

Language:

english

File:

PDF, 598 KB

english, 1998

6

Autosomal recessive inheritance of RYR1 mutations in a congenital myopathy with cores

Jungbluth, H., Muller, C. R., Halliger-Keller, B., Brockington, M., Brown, S. C., Feng, L., Chattopadhyay, A., Mercuri, E., Manzur, A. Y., Ferreiro, A., Laing, N. G., Davis, M. R., Roper, H. P., Dubow

Journal:

Year:

2002

Language:

english

File:

PDF, 399 KB

english, 2002

7

Clustering of FGFR2 gene mutations inpatients with Pfeiffer and Crouzon syndromes (FGFR2-associated craniosynostoses)

Kress, W., Collmann, H., B&uuml, sse, M., Halliger-Keller, B., Mueller, C.R.

Journal:

Cytogenetic and Genome Research

Year:

2000

Language:

english

File:

PDF, 185 KB

english, 2000

8

Minicore myopathy with ophthalmoplegia caused by mutations in the ryanodine receptor type 1 gene

Jungbluth, H., Zhou, H., Hartley, L., Halliger-Keller, B., Messina, S., Longman, C., Brockington, M., Robb, S. A., Straub, V., Voit, T., Swash, M., Ferreiro, A., Bydder, G., Sewry, C. A., Muller, C.,

Journal:

Year:

2005

Language:

english

File:

PDF, 1007 KB

english, 2005

9

Distribution and Structure of DM2 Repeat Tract Alleles in the German Population

Mahyera, Alexis S., Schneider, Tamara, Halliger-Keller, Birgit, Schrooten, Katja, Hörner, Eva-Maria, Rost, Simone, Kress, Wolfram

Journal:

Frontiers in Neurology

Year:

2018

Language:

english

File:

PDF, 1.19 MB

english, 2018