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Der Internist
|
July 1, 1997
[Liver transplantation in familial amyloid polyneuropathy. Case report and review of the literature]
M Krüger, K Altland, R P Linke, et al.
Progress in Clinical and Biological Research
|
January 1, 1982
Workshop on amniotic fluid Acetylcholinesterase
N Wald, R Harris, K Altland, et al.
The British Journal of Dermatology
|
November 9, 2000
A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family
S Cichon, R Kruse, A M Hillmer, et al.
Basic Research in Cardiology
|
November 1, 1991
Transthyretin Leu 68 in a form of cardiac amyloidosis
M R Almeida, A Hesse, A Steinmetz, et al.
American Journal of Human Genetics
|
May 1, 1991
Molecular analyses of an acidic transthyretin Asn 90 variant
M J Saraiva, M R Almeida, I L Alves, et al.
Clinical Genetics
|
January 1, 1996
Homozygosity and heterozygosity for the transthyretin Leu64 mutation: clinical, biochemical and molecular findings
A Ferlini, F Salvi, A Uncini, et al.
Lancet (London, England)
|
October 8, 1988
First-trimester biochemical screening for Down syndrome
H S Cuckle, N J Wald, G Barkai, et al.
Human Mutation
|
January 1, 1992
Two transthyretin variants (TTR Ala-49 and TTR Gln-89) in two Sicilian kindreds with hereditary amyloidosis
M R Almeida, A Ferlini, A Forabosco, et al.
The Journal of Clinical Endocrinology and Metabolism
|
August 1, 1993
Thyroxine binding in a TTR Met 119 kindred
I L Alves, C M Divino, G C Schussler, et al.
Human Genetics
|
December 1, 1988
Familial amyloidotic polyneuropathy: transthyretin (prealbumin) variants in kindreds of Italian origin
M J Saraiva, P P Costa, M do R Almeida, et al.
Page
of 5
Search research articles
Search
Showing results (41-50 of 50) with videos related to
Sort By:
Page
of 5
You have reached the last page of results.
This site can display upto 50 results.
Der Internist
|
July 1, 1997
[Liver transplantation in familial amyloid polyneuropathy. Case report and review of the literature]
M Krüger, K Altland, R P Linke, et al.
Progress in Clinical and Biological Research
|
January 1, 1982
Workshop on amniotic fluid Acetylcholinesterase
N Wald, R Harris, K Altland, et al.
The British Journal of Dermatology
|
November 9, 2000
A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family
S Cichon, R Kruse, A M Hillmer, et al.
Basic Research in Cardiology
|
November 1, 1991
Transthyretin Leu 68 in a form of cardiac amyloidosis
M R Almeida, A Hesse, A Steinmetz, et al.
American Journal of Human Genetics
|
May 1, 1991
Molecular analyses of an acidic transthyretin Asn 90 variant
M J Saraiva, M R Almeida, I L Alves, et al.
Clinical Genetics
|
January 1, 1996
Homozygosity and heterozygosity for the transthyretin Leu64 mutation: clinical, biochemical and molecular findings
A Ferlini, F Salvi, A Uncini, et al.
Lancet (London, England)
|
October 8, 1988
First-trimester biochemical screening for Down syndrome
H S Cuckle, N J Wald, G Barkai, et al.
Human Mutation
|
January 1, 1992
Two transthyretin variants (TTR Ala-49 and TTR Gln-89) in two Sicilian kindreds with hereditary amyloidosis
M R Almeida, A Ferlini, A Forabosco, et al.
The Journal of Clinical Endocrinology and Metabolism
|
August 1, 1993
Thyroxine binding in a TTR Met 119 kindred
I L Alves, C M Divino, G C Schussler, et al.
Human Genetics
|
December 1, 1988
Familial amyloidotic polyneuropathy: transthyretin (prealbumin) variants in kindreds of Italian origin
M J Saraiva, P P Costa, M do R Almeida, et al.
Page
of 5