B. Halliger–Keller

Autosomal recessive inheritance of <i>RYR1</i> mutations in a congenital myopathy with cores

Heinz Jungbluth, C. R. Müller, B. Halliger–Keller et al. · Neurology · 2002 · 165 citations

Life Sciences, Genetics, Molecular Genetics +15

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

Heinz Jungbluth, Haiyan Zhou, Louise Hartley et al. · Neurology · 2005 · 156 citations

Medicine, Genetics, Ophthalmology +15

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

H. Collmann, Madleen Busse, B. Halliger–Keller et al. · Cytogenetic and Genome Research · 2000 · 50 citations

Life Sciences, Genetics, Molecular Genetics +13

CCM1 gene deletion identified by MLPA in cerebral cavernous malformation

Sabine Gaetzner, Sonja Stahl, Oǧuzkan Sürücü et al. · Neurosurgical Review · 2006 · 30 citations

Medicine, Molecular Genetics, Neuroscience +14

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

Alexis S. Mahyera, Tamara Schneider, B. Halliger–Keller et al. · Frontiers in Neurology · 2018 · 23 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14