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Archives of Neurology
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May 1, 1995
Natural history in proximal spinal muscular atrophy. Clinical analysis of 445 patients and suggestions for a modification of existing classifications
K Zerres, S Rudnik-Schöneborn
Journal of Medical Genetics
|
June 1, 1994
A further patient with Pai syndrome with autosomal dominant inheritance?
S Rudnik-Schöneborn, K Zerres
Der Internist
|
March 14, 2012
[Cystic kidney diseases]
K Zerres, N Ortiz Brüchle
American Journal of Medical Genetics
|
October 1, 1989
Three sibs with achalasia and alacrimia: a separate entity different from triple-A syndrome
F Haverkamp, K Zerres, R Rosskamp
Annales De Genetique
|
January 1, 1990
Homozygosity of a 6/18 translocation in a hydatidiform mole
G Schwanitz, K Zerres, H Schüler
Human Genetics
|
January 1, 1985
Acquired cystic kidney disease--a possible pitfall in genetic counseling
K Zerres, R Albrecht, R Waldherr
Journal of Medical Genetics
|
July 1, 1993
Childhood onset autosomal dominant polycystic kidney disease in sibs: clinical picture and recurrence risk. German Working Group on Paediatric Nephrology (Arbeitsgemeinschaft für Pädiatrische Nephrologie
K Zerres, S Rudnik-Schöneborn, F Deget
Journal of the Neurological Sciences
|
January 1, 1992
Clinical variability of autosomal dominant spinal muscular atrophy
M Rietschel, S Rudnik-Schöneborn, K Zerres
Journal of Perinatal Medicine
|
October 17, 1998
Increased risk for abnormal placentation in women affected by myotonic dystrophy
S Rudnik-Schöneborn, D Röhrig, K Zerres
Clinical Genetics
|
May 1, 1995
Course of autosomal recessive polycystic kidney disease (ARPKD) in siblings: a clinical comparison of 20 sibships
F Deget, S Rudnik-Schöneborn, K Zerres
Page
of 18
Search research articles
Search
Showing results (11-20 of 174) with videos related to
Sort By:
Page
of 18
Archives of Neurology
|
May 1, 1995
Natural history in proximal spinal muscular atrophy. Clinical analysis of 445 patients and suggestions for a modification of existing classifications
K Zerres, S Rudnik-Schöneborn
Journal of Medical Genetics
|
June 1, 1994
A further patient with Pai syndrome with autosomal dominant inheritance?
S Rudnik-Schöneborn, K Zerres
Der Internist
|
March 14, 2012
[Cystic kidney diseases]
K Zerres, N Ortiz Brüchle
American Journal of Medical Genetics
|
October 1, 1989
Three sibs with achalasia and alacrimia: a separate entity different from triple-A syndrome
F Haverkamp, K Zerres, R Rosskamp
Annales De Genetique
|
January 1, 1990
Homozygosity of a 6/18 translocation in a hydatidiform mole
G Schwanitz, K Zerres, H Schüler
Human Genetics
|
January 1, 1985
Acquired cystic kidney disease--a possible pitfall in genetic counseling
K Zerres, R Albrecht, R Waldherr
Journal of Medical Genetics
|
July 1, 1993
Childhood onset autosomal dominant polycystic kidney disease in sibs: clinical picture and recurrence risk. German Working Group on Paediatric Nephrology (Arbeitsgemeinschaft für Pädiatrische Nephrologie
K Zerres, S Rudnik-Schöneborn, F Deget
Journal of the Neurological Sciences
|
January 1, 1992
Clinical variability of autosomal dominant spinal muscular atrophy
M Rietschel, S Rudnik-Schöneborn, K Zerres
Journal of Perinatal Medicine
|
October 17, 1998
Increased risk for abnormal placentation in women affected by myotonic dystrophy
S Rudnik-Schöneborn, D Röhrig, K Zerres
Clinical Genetics
|
May 1, 1995
Course of autosomal recessive polycystic kidney disease (ARPKD) in siblings: a clinical comparison of 20 sibships
F Deget, S Rudnik-Schöneborn, K Zerres
Page
of 18