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Journal of Molecular Medicine (Berlin, Germany)
|
May 20, 1998
Autosomal recessive polycystic kidney disease
K Zerres, S Rudnik-Schöneborn, C Steinkamm, et al.
Prenatal Diagnosis
|
May 1, 1995
Prenatal prediction in families with autosomal recessive proximal spinal muscular atrophy (5q11.2-q13.3): molecular genetics and clinical experience in 109 cases
B Wirth, S Rudnik-Schöneborn, E Hahnen, et al.
Neuromuscular Disorders : NMD
|
January 1, 1995
Exclusion of the gene locus for spinal muscular atrophy on chromosome 5q in a family with infantile olivopontocerebellar atrophy (OPCA) and anterior horn cell degeneration
S Rudnik-Schöneborn, B Wirth, D Röhrig, et al.
American Journal of Human Genetics
|
November 1, 1996
Hybrid survival motor neuron genes in patients with autosomal recessive spinal muscular atrophy: new insights into molecular mechanisms responsible for the disease
E Hahnen, J Schönling, S Rudnik-Schöneborn, et al.
American Journal of Medical Genetics
|
December 23, 1999
ADULT syndrome allelic to limb mammary syndrome (LMS)?
P Propping, W Friedl, T F Wienker, et al.
Neuropediatrics
|
February 1, 1996
Clinical spectrum and diagnostic criteria of infantile spinal muscular atrophy: further delineation on the basis of SMN gene deletion findings
S Rudnik-Schöneborn, R Forkert, E Hahnen, et al.
FEBS Letters
|
December 21, 1992
No genetic differences between affected and unaffected members of a German family with Leber's hereditary optic neuropathy (LHON) with respect to ten mtDNA point mutations associated with LHON
K D Gerbitz, A Paprotta, B Obermaier-Kusser, et al.
Brain Research. Molecular Brain Research
|
April 11, 2001
A point mutation in the human connexin32 promoter P2 does not correlate with X-linked dominant Charcot-Marie-Tooth neuropathy in Germany
C Bergmann, J M Schröder, S Rudnik-Schöneborn, et al.
Human Genetics
|
May 1, 1992
Chromosomal findings in fetuses with prenatally diagnosed cysts of the choroid plexus
K Zerres, H Schüler, U Gembruch, et al.
Neuroscience
|
March 31, 2010
Medial temporal lobe dysfunction during encoding and retrieval of episodic memory in non-demented APOE epsilon4 carriers
J Kukolja, C M Thiel, T Eggermann, et al.
Page
of 18
Search research articles
Search
Showing results (61-70 of 174) with videos related to
Sort By:
Page
of 18
Journal of Molecular Medicine (Berlin, Germany)
|
May 20, 1998
Autosomal recessive polycystic kidney disease
K Zerres, S Rudnik-Schöneborn, C Steinkamm, et al.
Prenatal Diagnosis
|
May 1, 1995
Prenatal prediction in families with autosomal recessive proximal spinal muscular atrophy (5q11.2-q13.3): molecular genetics and clinical experience in 109 cases
B Wirth, S Rudnik-Schöneborn, E Hahnen, et al.
Neuromuscular Disorders : NMD
|
January 1, 1995
Exclusion of the gene locus for spinal muscular atrophy on chromosome 5q in a family with infantile olivopontocerebellar atrophy (OPCA) and anterior horn cell degeneration
S Rudnik-Schöneborn, B Wirth, D Röhrig, et al.
American Journal of Human Genetics
|
November 1, 1996
Hybrid survival motor neuron genes in patients with autosomal recessive spinal muscular atrophy: new insights into molecular mechanisms responsible for the disease
E Hahnen, J Schönling, S Rudnik-Schöneborn, et al.
American Journal of Medical Genetics
|
December 23, 1999
ADULT syndrome allelic to limb mammary syndrome (LMS)?
P Propping, W Friedl, T F Wienker, et al.
Neuropediatrics
|
February 1, 1996
Clinical spectrum and diagnostic criteria of infantile spinal muscular atrophy: further delineation on the basis of SMN gene deletion findings
S Rudnik-Schöneborn, R Forkert, E Hahnen, et al.
FEBS Letters
|
December 21, 1992
No genetic differences between affected and unaffected members of a German family with Leber's hereditary optic neuropathy (LHON) with respect to ten mtDNA point mutations associated with LHON
K D Gerbitz, A Paprotta, B Obermaier-Kusser, et al.
Brain Research. Molecular Brain Research
|
April 11, 2001
A point mutation in the human connexin32 promoter P2 does not correlate with X-linked dominant Charcot-Marie-Tooth neuropathy in Germany
C Bergmann, J M Schröder, S Rudnik-Schöneborn, et al.
Human Genetics
|
May 1, 1992
Chromosomal findings in fetuses with prenatally diagnosed cysts of the choroid plexus
K Zerres, H Schüler, U Gembruch, et al.
Neuroscience
|
March 31, 2010
Medial temporal lobe dysfunction during encoding and retrieval of episodic memory in non-demented APOE epsilon4 carriers
J Kukolja, C M Thiel, T Eggermann, et al.
Page
of 18