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The Journal of Heredity
|
May 1, 1996
Derivation and characterization of a somatic cell hybrid containing the portion of mouse chromosome 11 (MMU11) homologous to human chromosome 17q
D J Morris-Rosendahl, G Schriever-Schwemmer, T J Robinson
Psychiatric Genetics
|
August 1, 1998
No association between the tyrosine hydroxylase microsatellite marker HUMTH01 and schizophrenia or bipolar I disorder
E Burgert, M A Crocq, E Bausch, et al.
Klinische Padiatrie
|
October 26, 2013
Dilatative uropathy as a manifestation of neurohypophyseal diabetes insipidus due to a novel mutation in the arginine vasopressin-neurophysin-II gene
V Lindenthal, A Mainberger, D J Morris-Rosendahl, et al.
Genetic Counseling (Geneva, Switzerland)
|
February 9, 2016
RECURRENT RAB3GAP1 MUTATIONS IN THE TURKISH POPULATION
S Tasdemir, I Sahin, D J Morris-Rosendahl, et al.
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology
|
December 16, 2000
Stable methylation patterns in interspecific antelope hybrids and the characterization and localization of a satellite fraction in the Alcelaphini and Hippotragini
T J Robinson, O Wittekindt, J J Pasantes, et al.
American Journal of Medical Genetics
|
May 31, 1997
Analysis of the CAG repeats in the SCA1 and B37 genes in schizophrenic and bipolar I disorder patients: tentative association between B37 and schizophrenia
D J Morris-Rosendahl, E Burgert, G Uyanik, et al.
Psychiatric Genetics
|
July 21, 1999
hSKCa3: a candidate gene for schizophrenia?
B Meissner, S Purmann, M Schürmann, et al.
Molecular Psychiatry
|
March 10, 1998
Isolation of a novel potassium channel gene hSKCa3 containing a polymorphic CAG repeat: a candidate for schizophrenia and bipolar disorder?
K G Chandy, E Fantino, O Wittekindt, et al.
Molecular Syndromology
|
October 30, 2010
Disturbed Wnt Signalling due to a Mutation in CCDC88C Causes an Autosomal Recessive Non-Syndromic Hydrocephalus with Medial Diverticulum
A B Ekici, D Hilfinger, M Jatzwauk, et al.
Molecular Psychiatry
|
July 8, 1999
Association between hSKCa3 and schizophrenia not confirmed by transmission disequilibrium test in 193 offspring/parents trios
O Wittekindt, S G Schwab, E Burgert, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 14) with videos related to
Sort By:
Page
of 2
The Journal of Heredity
|
May 1, 1996
Derivation and characterization of a somatic cell hybrid containing the portion of mouse chromosome 11 (MMU11) homologous to human chromosome 17q
D J Morris-Rosendahl, G Schriever-Schwemmer, T J Robinson
Psychiatric Genetics
|
August 1, 1998
No association between the tyrosine hydroxylase microsatellite marker HUMTH01 and schizophrenia or bipolar I disorder
E Burgert, M A Crocq, E Bausch, et al.
Klinische Padiatrie
|
October 26, 2013
Dilatative uropathy as a manifestation of neurohypophyseal diabetes insipidus due to a novel mutation in the arginine vasopressin-neurophysin-II gene
V Lindenthal, A Mainberger, D J Morris-Rosendahl, et al.
Genetic Counseling (Geneva, Switzerland)
|
February 9, 2016
RECURRENT RAB3GAP1 MUTATIONS IN THE TURKISH POPULATION
S Tasdemir, I Sahin, D J Morris-Rosendahl, et al.
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology
|
December 16, 2000
Stable methylation patterns in interspecific antelope hybrids and the characterization and localization of a satellite fraction in the Alcelaphini and Hippotragini
T J Robinson, O Wittekindt, J J Pasantes, et al.
American Journal of Medical Genetics
|
May 31, 1997
Analysis of the CAG repeats in the SCA1 and B37 genes in schizophrenic and bipolar I disorder patients: tentative association between B37 and schizophrenia
D J Morris-Rosendahl, E Burgert, G Uyanik, et al.
Psychiatric Genetics
|
July 21, 1999
hSKCa3: a candidate gene for schizophrenia?
B Meissner, S Purmann, M Schürmann, et al.
Molecular Psychiatry
|
March 10, 1998
Isolation of a novel potassium channel gene hSKCa3 containing a polymorphic CAG repeat: a candidate for schizophrenia and bipolar disorder?
K G Chandy, E Fantino, O Wittekindt, et al.
Molecular Syndromology
|
October 30, 2010
Disturbed Wnt Signalling due to a Mutation in CCDC88C Causes an Autosomal Recessive Non-Syndromic Hydrocephalus with Medial Diverticulum
A B Ekici, D Hilfinger, M Jatzwauk, et al.
Molecular Psychiatry
|
July 8, 1999
Association between hSKCa3 and schizophrenia not confirmed by transmission disequilibrium test in 193 offspring/parents trios
O Wittekindt, S G Schwab, E Burgert, et al.
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of 2