Search research articles
Contact Us
Filters
Showing results (101-110 of 105) with videos related to
Page
of 11
Sort By:
You have reached the last page of results.
This site can display upto 105 results.
Bone Marrow Transplantation
|
February 5, 2013
CD34(+) lineage specific donor cell chimerism for the diagnosis and treatment of impending relapse of AML or myelodysplastic syndrome after allo-SCT
F Rosenow, A Berkemeier, U Krug, et al.
Genomics
|
May 18, 1999
The presynaptic cytomatrix protein Bassoon: sequence and chromosomal localization of the human BSN gene
C Winter, S tom Dieck, T M Boeckers, et al.
Journal of Pediatric Urology
|
February 5, 2019
Variations of sex development: The first German interdisciplinary consensus paper
S Krege, F Eckoldt, A Richter-Unruh, et al.
Clinical Genetics
|
September 17, 2011
BRCA1/2 testing: uptake, phenocopies, and strategies to improve detection rates in initially negative families
C Fischer, C Engel, C Sutter, et al.
Molecular Psychiatry
|
February 4, 2015
X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genes
H Hu, S A Haas, J Chelly, et al.
Page
of 11
Search research articles
Search
Showing results (101-110 of 105) with videos related to
Sort By:
Page
of 11
You have reached the last page of results.
This site can display upto 105 results.
Bone Marrow Transplantation
|
February 5, 2013
CD34(+) lineage specific donor cell chimerism for the diagnosis and treatment of impending relapse of AML or myelodysplastic syndrome after allo-SCT
F Rosenow, A Berkemeier, U Krug, et al.
Genomics
|
May 18, 1999
The presynaptic cytomatrix protein Bassoon: sequence and chromosomal localization of the human BSN gene
C Winter, S tom Dieck, T M Boeckers, et al.
Journal of Pediatric Urology
|
February 5, 2019
Variations of sex development: The first German interdisciplinary consensus paper
S Krege, F Eckoldt, A Richter-Unruh, et al.
Clinical Genetics
|
September 17, 2011
BRCA1/2 testing: uptake, phenocopies, and strategies to improve detection rates in initially negative families
C Fischer, C Engel, C Sutter, et al.
Molecular Psychiatry
|
February 4, 2015
X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genes
H Hu, S A Haas, J Chelly, et al.
Page
of 11