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Marine Pollution Bulletin
|
September 22, 2007
Survey of estrogenic and androgenic disruption in Swedish coastal waters by the analysis of bile fluid from perch and biomarkers in the three-spined stickleback
Maria Pettersson, Edda Hahlbeck, Ioanna Katsiadaki, et al.
Mutation Research
|
November 2, 2018
Flanking complex copy number variants in the same family formed through unequal crossing-over during meiosis
Maria Pettersson, Jesper Eisfeldt, Elisabeth Syk Lundberg, et al.
Human Genetics
|
December 14, 2020
Hybrid sequencing resolves two germline ultra-complex chromosomal rearrangements consisting of 137 breakpoint junctions in a single carrier
Jesper Eisfeldt, Maria Pettersson, Anna Petri, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
January 16, 2021
Lissencephaly in an epilepsy cohort: Molecular, radiological and clinical aspects
Sintia Kolbjer, Daniel A Martin, Maria Pettersson, et al.
Annals of Biomedical Engineering
|
September 25, 2015
Surface and Subsurface Analyses of Metal-on-Polyethylene Total Hip Replacement Retrievals
Vicky Vuong, Maria Pettersson, Cecilia Persson, et al.
Pediatric Surgery International
|
May 25, 2026
Rare variants in TTC7A, ROCK2 and LIMK2 suggest a role for the ROCK-signaling pathway in isolated intestinal malrotation
Karin Salehi Karlslätt, Maria Pettersson, Kristina Lagerstedt-Robinson, et al.
Materials Science & Engineering. C, Materials for Biological Applications
|
March 9, 2016
Dissolution behaviour of silicon nitride coatings for joint replacements
Maria Pettersson, Michael Bryant, Susann Schmidt, et al.
American Journal of Medical Genetics. Part A
|
March 21, 2017
Further evidence for specific IFIH1 mutation as a cause of Singleton-Merten syndrome with phenotypic heterogeneity
Maria Pettersson, Birgitta Bergendal, Johanna Norderyd, et al.
Materials (Basel, Switzerland)
|
August 5, 2017
Influence of Substrate Heating and Nitrogen Flow on the Composition, Morphological and Mechanical Properties of SiN<sub>x</sub> Coatings Aimed for Joint Replacements
Charlotte Skjöldebrand, Susann Schmidt, Vicky Vuong, et al.
Human Mutation
|
December 30, 2017
Targeted copy number screening highlights an intragenic deletion of WDR63 as the likely cause of human occipital encephalocele and abnormal CNS development in zebrafish
Wolfgang Hofmeister, Maria Pettersson, Deniz Kurtoglu, et al.
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of 6
Search research articles
Search
Showing results (11-20 of 54) with videos related to
Sort By:
Page
of 6
Marine Pollution Bulletin
|
September 22, 2007
Survey of estrogenic and androgenic disruption in Swedish coastal waters by the analysis of bile fluid from perch and biomarkers in the three-spined stickleback
Maria Pettersson, Edda Hahlbeck, Ioanna Katsiadaki, et al.
Mutation Research
|
November 2, 2018
Flanking complex copy number variants in the same family formed through unequal crossing-over during meiosis
Maria Pettersson, Jesper Eisfeldt, Elisabeth Syk Lundberg, et al.
Human Genetics
|
December 14, 2020
Hybrid sequencing resolves two germline ultra-complex chromosomal rearrangements consisting of 137 breakpoint junctions in a single carrier
Jesper Eisfeldt, Maria Pettersson, Anna Petri, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
January 16, 2021
Lissencephaly in an epilepsy cohort: Molecular, radiological and clinical aspects
Sintia Kolbjer, Daniel A Martin, Maria Pettersson, et al.
Annals of Biomedical Engineering
|
September 25, 2015
Surface and Subsurface Analyses of Metal-on-Polyethylene Total Hip Replacement Retrievals
Vicky Vuong, Maria Pettersson, Cecilia Persson, et al.
Pediatric Surgery International
|
May 25, 2026
Rare variants in TTC7A, ROCK2 and LIMK2 suggest a role for the ROCK-signaling pathway in isolated intestinal malrotation
Karin Salehi Karlslätt, Maria Pettersson, Kristina Lagerstedt-Robinson, et al.
Materials Science & Engineering. C, Materials for Biological Applications
|
March 9, 2016
Dissolution behaviour of silicon nitride coatings for joint replacements
Maria Pettersson, Michael Bryant, Susann Schmidt, et al.
American Journal of Medical Genetics. Part A
|
March 21, 2017
Further evidence for specific IFIH1 mutation as a cause of Singleton-Merten syndrome with phenotypic heterogeneity
Maria Pettersson, Birgitta Bergendal, Johanna Norderyd, et al.
Materials (Basel, Switzerland)
|
August 5, 2017
Influence of Substrate Heating and Nitrogen Flow on the Composition, Morphological and Mechanical Properties of SiN<sub>x</sub> Coatings Aimed for Joint Replacements
Charlotte Skjöldebrand, Susann Schmidt, Vicky Vuong, et al.
Human Mutation
|
December 30, 2017
Targeted copy number screening highlights an intragenic deletion of WDR63 as the likely cause of human occipital encephalocele and abnormal CNS development in zebrafish
Wolfgang Hofmeister, Maria Pettersson, Deniz Kurtoglu, et al.
Page
of 6