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Genomics
|
July 1, 1994
Identification of key recombinants in multiplex SMA families
G van der Steege, J M Cobben, C Brahe, et al.
American Journal of Medical Genetics
|
May 17, 1996
Molecular and cytogenetic characterization of a recurrent unbalanced translocation (4;21)(p16.3;q22.1): relevance to the Wolf-Hirschhorn and Down syndrome critical regions
G Sebastio, L Perone, V Guzzetta, et al.
Human Genetics
|
May 1, 1994
Mapping of two new markers within the smallest interval harboring the spinal muscular atrophy locus by family and radiation hybrid analysis
C Brahe, I Velonà, G van der Steege, et al.
American Journal of Human Genetics
|
October 1, 1996
Apparent gene conversions involving the SMN gene in the region of the spinal muscular atrophy locus on chromosome 5
G van der Steege, P M Grootscholten, J M Cobben, et al.
Genomics
|
May 8, 1998
Construction of a 2.5-Mb integrated physical and gene map of distal 21q22.3
V Lapenta, V Sossi, P Gosset, et al.
Human Genetics
|
December 1, 1986
Assignment of human transcobalamin II (TC2) to chromosome 22 using somatic cell hybrids and monosomic meningioma cells
F Arwert, H J Porck, M Fràter-Schröder, et al.
European Journal of Human Genetics : EJHG
|
January 1, 1995
A provisional transcript map of the spinal muscular atrophy (SMA) critical region
G van der Steege, T G Draaijers, P M Grootscholten, et al.
Neuromuscular Disorders : NMD
|
April 17, 2007
The Hammersmith functional score correlates with the SMN2 copy number: a multicentric study
F D Tiziano, E Bertini, S Messina, et al.
Neurology
|
November 4, 2006
Randomized, double-blind, placebo-controlled trial of phenylbutyrate in spinal muscular atrophy
E Mercuri, E Bertini, S Messina, et al.
Page
of 5
Search research articles
Search
Showing results (41-50 of 49) with videos related to
Sort By:
Page
of 5
You have reached the last page of results.
This site can display upto 49 results.
Genomics
|
July 1, 1994
Identification of key recombinants in multiplex SMA families
G van der Steege, J M Cobben, C Brahe, et al.
American Journal of Medical Genetics
|
May 17, 1996
Molecular and cytogenetic characterization of a recurrent unbalanced translocation (4;21)(p16.3;q22.1): relevance to the Wolf-Hirschhorn and Down syndrome critical regions
G Sebastio, L Perone, V Guzzetta, et al.
Human Genetics
|
May 1, 1994
Mapping of two new markers within the smallest interval harboring the spinal muscular atrophy locus by family and radiation hybrid analysis
C Brahe, I Velonà, G van der Steege, et al.
American Journal of Human Genetics
|
October 1, 1996
Apparent gene conversions involving the SMN gene in the region of the spinal muscular atrophy locus on chromosome 5
G van der Steege, P M Grootscholten, J M Cobben, et al.
Genomics
|
May 8, 1998
Construction of a 2.5-Mb integrated physical and gene map of distal 21q22.3
V Lapenta, V Sossi, P Gosset, et al.
Human Genetics
|
December 1, 1986
Assignment of human transcobalamin II (TC2) to chromosome 22 using somatic cell hybrids and monosomic meningioma cells
F Arwert, H J Porck, M Fràter-Schröder, et al.
European Journal of Human Genetics : EJHG
|
January 1, 1995
A provisional transcript map of the spinal muscular atrophy (SMA) critical region
G van der Steege, T G Draaijers, P M Grootscholten, et al.
Neuromuscular Disorders : NMD
|
April 17, 2007
The Hammersmith functional score correlates with the SMN2 copy number: a multicentric study
F D Tiziano, E Bertini, S Messina, et al.
Neurology
|
November 4, 2006
Randomized, double-blind, placebo-controlled trial of phenylbutyrate in spinal muscular atrophy
E Mercuri, E Bertini, S Messina, et al.
Page
of 5