Suchergebnisse - "Szafranski, Przemyslaw"

PubPharm (132)

51

Erratum to: Haploinsufficiency of the E3 ubiquitin-protein ligase gene TRIP12 causes intellectual disability with or without autism spectrum disorders, speech delay, and dysmorphic features

enthalten in: Human genetics | 2017

von Zhang, J. | Gambin, T. | Yuan, B. | +35

52

CRISPR/Cas9-mediated deletion of lncRNA Gm26878 in the distant Foxf1 enhancer region

enthalten in: Mammalian genome | 2017

von Szafranski, P. | Karolak, J. | Lanza, D. | +3

53

CRISPR/Cas9-mediated deletion of lncRNA Gm26878 in the distant Foxf1 enhancer region

enthalten in: Mammalian genome | 2017

von Szafranski, P. | Karolak, J. | Lanza, D. | +3

54

CRISPR/Cas9-mediated deletion of lncRNA Gm26878 in the distant Foxf1 enhancer region

enthalten in: Mammalian genome | 2017

von Szafranski, P. | Karolak, J. | Lanza, D. | +3

55

Assessment of the chromatographic lipophilicity of eight cephalosporins on different stationary phases

enthalten in: European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences | 2017

von Dąbrowska, M. | Starek, M. | Komsta, �. | +3

56

Haploinsufficiency of the E3 ubiquitin-protein ligase gene TRIP12 causes intellectual disability with or without autism spectrum disorders, speech delay, and dysmorphic features

enthalten in: Human genetics | 2017

von Zhang, J. | Gambin, T. | Yuan, B. | +35

ErratumIn: Hum Genet. 2017 Jun 28;:. - PMID 28660352

57

Evolutionarily recent, insertional fission of mitochondrial cox2 into complementary genes in bilaterian Metazoa

enthalten in: BMC genomics | 2017

von Szafranski, P.

58

Evolutionarily recent, insertional fission of mitochondrial cox2 into complementary genes in bilaterian Metazoa

enthalten in: BMC genomics | 2017

von Szafranski, P.

59

Evolutionarily recent, insertional fission of mitochondrial cox2 into complementary genes in bilaterian Metazoa

enthalten in: BMC genomics | 2017

von Szafranski, P.

60

Haploinsufficiency of the E3 ubiquitin-protein ligase gene TRIP12 causes intellectual disability with or without autism spectrum disorders, speech delay, and dysmorphic features

enthalten in: Human genetics | 2017

von Zhang, J. | Gambin, T. | Yuan, B. | +35