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Prenatal Diagnosis
|
July 27, 1999
Tuberous sclerosis with intracardiac rhabdomyoma in a fetus with trisomy 21: case report and review of literature
M Krapp, A A Baschat, U Gembruch, et al.
Human Mutation
|
January 1, 1995
Mucopolysaccharidosis type I: identification of 13 novel mutations of the alpha-L-iduronidase gene
S Bunge, W J Kleijer, C Steglich, et al.
Respiratory Medicine
|
July 11, 1998
HLA-DQB1 and HLA-DPB1 genotypes in familial sarcoidosis
M Schürmann, G Bein, D Kirsten, et al.
The Journal of Clinical Endocrinology and Metabolism
|
April 1, 1982
Clinical, endocrinological, and cytological characterization of two 46, XX males
H U Schweikert, L Weissbach, G Leyendecker, et al.
Journal of Assisted Reproduction and Genetics
|
July 29, 2004
Low-level gonosomal mosaicism in women undergoing ICSI cycles
R Voigt, A K Schröder, E Hinrichs, et al.
Genomics
|
July 1, 1991
Analysis of a dystrophin gene deletion by amplification of mRNA isolated from DMD myotubes cultured in vitro
J Ehrenpreis, M Hillers, B Junkes, et al.
Journal of Neurology
|
June 11, 2003
Refinement of the spinocerebellar ataxia type 4 locus in a large German family and exclusion of CAG repeat expansions in this region
Y Hellenbroich, S Bubel, H Pawlack, et al.
American Journal of Respiratory and Critical Care Medicine
|
September 11, 2001
Results from a genome-wide search for predisposing genes in sarcoidosis
M Schürmann, P Reichel, B Müller-Myhsok, et al.
Genomics
|
October 1, 1991
Pro-347-Arg mutation of the rhodopsin gene in autosomal dominant retinitis pigmentosa
A Gal, A Artlich, M Ludwig, et al.
American Heart Journal
|
November 1, 1989
Right atrial papillary fibroelastoma: diagnosis by transthoracic and transesophageal echocardiography and percutaneous transvenous biopsy
M E Schwinger, E Katz, H Rotterdam, et al.
Page
of 22
Search research articles
Search
Showing results (131-140 of 213) with videos related to
Sort By:
Page
of 22
Prenatal Diagnosis
|
July 27, 1999
Tuberous sclerosis with intracardiac rhabdomyoma in a fetus with trisomy 21: case report and review of literature
M Krapp, A A Baschat, U Gembruch, et al.
Human Mutation
|
January 1, 1995
Mucopolysaccharidosis type I: identification of 13 novel mutations of the alpha-L-iduronidase gene
S Bunge, W J Kleijer, C Steglich, et al.
Respiratory Medicine
|
July 11, 1998
HLA-DQB1 and HLA-DPB1 genotypes in familial sarcoidosis
M Schürmann, G Bein, D Kirsten, et al.
The Journal of Clinical Endocrinology and Metabolism
|
April 1, 1982
Clinical, endocrinological, and cytological characterization of two 46, XX males
H U Schweikert, L Weissbach, G Leyendecker, et al.
Journal of Assisted Reproduction and Genetics
|
July 29, 2004
Low-level gonosomal mosaicism in women undergoing ICSI cycles
R Voigt, A K Schröder, E Hinrichs, et al.
Genomics
|
July 1, 1991
Analysis of a dystrophin gene deletion by amplification of mRNA isolated from DMD myotubes cultured in vitro
J Ehrenpreis, M Hillers, B Junkes, et al.
Journal of Neurology
|
June 11, 2003
Refinement of the spinocerebellar ataxia type 4 locus in a large German family and exclusion of CAG repeat expansions in this region
Y Hellenbroich, S Bubel, H Pawlack, et al.
American Journal of Respiratory and Critical Care Medicine
|
September 11, 2001
Results from a genome-wide search for predisposing genes in sarcoidosis
M Schürmann, P Reichel, B Müller-Myhsok, et al.
Genomics
|
October 1, 1991
Pro-347-Arg mutation of the rhodopsin gene in autosomal dominant retinitis pigmentosa
A Gal, A Artlich, M Ludwig, et al.
American Heart Journal
|
November 1, 1989
Right atrial papillary fibroelastoma: diagnosis by transthoracic and transesophageal echocardiography and percutaneous transvenous biopsy
M E Schwinger, E Katz, H Rotterdam, et al.
Page
of 22