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International Journal of Legal Medicine
|
January 1, 1996
The validation of a 7-locus multiplex STR test for use in forensic casework. (II), Artefacts, casework studies and success rates
R Sparkes, C Kimpton, S Gilbard, et al.
Journal of Forensic Sciences
|
July 17, 1999
Validation studies of an immunochromatographic 1-step test for the forensic identification of human blood
M N Hochmeister, B Budowle, R Sparkes, et al.
Blood
|
September 1, 1976
Successful bone marrow transplantation against mixed lymphocyte culture barrier
S A Feig, G Opelz, H S Winter, et al.
The Journal of Experimental Biology
|
March 11, 2025
Sex-specific performance, trade-offs and trait repeatability across the lifetime of the world's largest semelparous mammal (Dasyurus hallucatus)
Gabriella R Sparkes, Jaime Heiniger, Nicholas M A Smith, et al.
Epilepsia
|
January 1, 1990
Gene mapping in the idiopathic generalized epilepsies: juvenile myoclonic epilepsy, childhood absence epilepsy, epilepsy with grand mal seizures, and early childhood myoclonic epilepsy
A V Delgado-Escueta, D Greenberg, K Weissbecker, et al.
Animals : an Open Access Journal From MDPI
|
December 30, 2025
Between the Trees: Quantifying Koala Ground Movement for Conservation Action
Gabriella R Sparkes, Oakleigh Wilson, William A Ellis, et al.
Progress in Clinical and Biological Research
|
January 1, 1989
The human alpha 2-alpha 1-theta 1 globin locus: some thoughts and recent studies of its evolution and regulation
C C Shen, A Bailey, J H Kim, et al.
American Journal of Medical Genetics
|
February 15, 1994
U-type exchange in a paracentric inversion as a possible mechanism of origin of an inverted tandem duplication of chromosome 8
J J Mitchell, M Vekemans, S Luscombe, et al.
Epilepsy Research. Supplement
|
January 1, 1991
The choice of epilepsy syndromes for genetic analysis
A V Delgado-Escueta, D A Greenberg, K Weissbecker, et al.
Cell
|
November 5, 1993
A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosis
E W Jabs, U Müller, X Li, et al.
Page
of 4
Search research articles
Search
Showing results (21-30 of 37) with videos related to
Sort By:
Page
of 4
International Journal of Legal Medicine
|
January 1, 1996
The validation of a 7-locus multiplex STR test for use in forensic casework. (II), Artefacts, casework studies and success rates
R Sparkes, C Kimpton, S Gilbard, et al.
Journal of Forensic Sciences
|
July 17, 1999
Validation studies of an immunochromatographic 1-step test for the forensic identification of human blood
M N Hochmeister, B Budowle, R Sparkes, et al.
Blood
|
September 1, 1976
Successful bone marrow transplantation against mixed lymphocyte culture barrier
S A Feig, G Opelz, H S Winter, et al.
The Journal of Experimental Biology
|
March 11, 2025
Sex-specific performance, trade-offs and trait repeatability across the lifetime of the world's largest semelparous mammal (Dasyurus hallucatus)
Gabriella R Sparkes, Jaime Heiniger, Nicholas M A Smith, et al.
Epilepsia
|
January 1, 1990
Gene mapping in the idiopathic generalized epilepsies: juvenile myoclonic epilepsy, childhood absence epilepsy, epilepsy with grand mal seizures, and early childhood myoclonic epilepsy
A V Delgado-Escueta, D Greenberg, K Weissbecker, et al.
Animals : an Open Access Journal From MDPI
|
December 30, 2025
Between the Trees: Quantifying Koala Ground Movement for Conservation Action
Gabriella R Sparkes, Oakleigh Wilson, William A Ellis, et al.
Progress in Clinical and Biological Research
|
January 1, 1989
The human alpha 2-alpha 1-theta 1 globin locus: some thoughts and recent studies of its evolution and regulation
C C Shen, A Bailey, J H Kim, et al.
American Journal of Medical Genetics
|
February 15, 1994
U-type exchange in a paracentric inversion as a possible mechanism of origin of an inverted tandem duplication of chromosome 8
J J Mitchell, M Vekemans, S Luscombe, et al.
Epilepsy Research. Supplement
|
January 1, 1991
The choice of epilepsy syndromes for genetic analysis
A V Delgado-Escueta, D A Greenberg, K Weissbecker, et al.
Cell
|
November 5, 1993
A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosis
E W Jabs, U Müller, X Li, et al.
Page
of 4