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Human Genetics
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October 1, 1988
Linkage analysis in X-linked ichthyosis (steroid sulfatase deficiency)
B Wirth, F H Herrmann, M Neugebauer, et al.
Cancer
|
February 15, 1995
The relationship of human papillomavirus to proliferation and ploidy in carcinoma of the anus
A E Noffsinger, Y Z Hui, L Suzuk, et al.
The Journal of Biological Chemistry
|
August 15, 1988
Albumin and alpha-fetoprotein gene expression in various nonhepatic rat tissues
J L Nahon, I Tratner, A Poliard, et al.
Neuropediatrics
|
August 12, 2003
Degree of hypomyelination and magnetic resonance spectroscopy findings in patients with Pelizaeus Merzbacher phenotype
B Plecko, S Stöckler-Ipsiroglu, S Gruber, et al.
The Journal of Thoracic and Cardiovascular Surgery
|
April 16, 1998
Angiogenesis as a predictor of survival after surgical resection for stage I non-small-cell lung cancer
I G Duarte, B L Bufkin, M F Pennington, et al.
Acta Crystallographica. Section C, Crystal Structure Communications
|
December 6, 2008
The absolute configuration of 1-epialexine hemihydrate
Amber L Thompson, David J Watkin, Zoltan A Gal, et al.
Genomics
|
April 18, 1998
Homozygosity mapping of autosomal recessive retinitis pigmentosa locus (RP22) on chromosome 16p12.1-p12.3
U Finckh, S Xu, G Kumaramanickavel, et al.
Cytogenetics and Cell Genetics
|
February 15, 2001
Cloning and characterization of the breakpoint regions of a chromosome 11;18 translocation in a patient with hamartoma of the retinal pigment epithelium
K Kutsche, E Glauner, S Knauf, et al.
Clinical Genetics
|
March 18, 2004
The Mainz Severity Score Index: a new instrument for quantifying the Anderson-Fabry disease phenotype, and the response of patients to enzyme replacement therapy
C Whybra, C Kampmann, F Krummenauer, et al.
Human Molecular Genetics
|
June 1, 1994
Mucopolysaccharidosis type I: identification of 8 novel mutations and determination of the frequency of the two common alpha-L-iduronidase mutations (W402X and Q70X) among European patients
S Bunge, W J Kleijer, C Steglich, et al.
Page
of 49
Search research articles
Search
Showing results (391-400 of 488) with videos related to
Sort By:
Page
of 49
Human Genetics
|
October 1, 1988
Linkage analysis in X-linked ichthyosis (steroid sulfatase deficiency)
B Wirth, F H Herrmann, M Neugebauer, et al.
Cancer
|
February 15, 1995
The relationship of human papillomavirus to proliferation and ploidy in carcinoma of the anus
A E Noffsinger, Y Z Hui, L Suzuk, et al.
The Journal of Biological Chemistry
|
August 15, 1988
Albumin and alpha-fetoprotein gene expression in various nonhepatic rat tissues
J L Nahon, I Tratner, A Poliard, et al.
Neuropediatrics
|
August 12, 2003
Degree of hypomyelination and magnetic resonance spectroscopy findings in patients with Pelizaeus Merzbacher phenotype
B Plecko, S Stöckler-Ipsiroglu, S Gruber, et al.
The Journal of Thoracic and Cardiovascular Surgery
|
April 16, 1998
Angiogenesis as a predictor of survival after surgical resection for stage I non-small-cell lung cancer
I G Duarte, B L Bufkin, M F Pennington, et al.
Acta Crystallographica. Section C, Crystal Structure Communications
|
December 6, 2008
The absolute configuration of 1-epialexine hemihydrate
Amber L Thompson, David J Watkin, Zoltan A Gal, et al.
Genomics
|
April 18, 1998
Homozygosity mapping of autosomal recessive retinitis pigmentosa locus (RP22) on chromosome 16p12.1-p12.3
U Finckh, S Xu, G Kumaramanickavel, et al.
Cytogenetics and Cell Genetics
|
February 15, 2001
Cloning and characterization of the breakpoint regions of a chromosome 11;18 translocation in a patient with hamartoma of the retinal pigment epithelium
K Kutsche, E Glauner, S Knauf, et al.
Clinical Genetics
|
March 18, 2004
The Mainz Severity Score Index: a new instrument for quantifying the Anderson-Fabry disease phenotype, and the response of patients to enzyme replacement therapy
C Whybra, C Kampmann, F Krummenauer, et al.
Human Molecular Genetics
|
June 1, 1994
Mucopolysaccharidosis type I: identification of 8 novel mutations and determination of the frequency of the two common alpha-L-iduronidase mutations (W402X and Q70X) among European patients
S Bunge, W J Kleijer, C Steglich, et al.
Page
of 49