Jutta Schönling

Molecular analysis of candidate genes on chromosome 5q13 in autosomal recessive spinal muscular atrophy: evidence of homozygous deletions of the SMN gene in unaffected individuals

Eric Hahnen, Randolf Forkert, Christine Marke et al. · Human Molecular Genetics · 1995 · 286 citations

De Novo Rearrangements Found in 2% of Index Patients with Spinal Muscular Atrophy: Mutational Mechanisms, Parental Origin, Mutation Rate, and Implications for Genetic Counseling

Brunhilde Wirth, Thorsten Schmidt, Eric Hahnen et al. · The American Journal of Human Genetics · 1997 · 176 citations · Full text

Index Patients, Mendelian Disorder, Genetic Disorder +5

Hybrid survival motor neuron genes in patients with autosomal recessive spinal muscular atrophy: new insights into molecular mechanisms responsible for the disease.

Eric Hahnen, Jutta Schönling, Sabine Rudnik‐Schöneborn et al. · PubMed · 1996 · 137 citations

Missense Mutations in Exon 6 of the Survival Motor Neuron Gene in Patients with Spinal Muscular Atrophy (SMA)

Eric Hahnen, Jutta Schönling, Sabine Rudnik‐Schöneborn et al. · Human Molecular Genetics · 1997 · 109 citations · Full text

Molecular characterization of a new plasmid-encoded SHV-type  -lactamase (SHV-2 variant) conferring high-level cefotaxime resistance upon Klebsiella pneumoniae

Andreas Podbielski, Jutta Schönling, B. Melzer et al. · Journal of General Microbiology · 1991 · 48 citations