Suchergebnisse - "Szafranski, Przemyslaw"

PubPharm (132)

101

Chromosome conformation capture-on-chip analysis of long-range cis-interactions of the SOX9 promoter

enthalten in: Chromosome research | 2013

von Smyk, M. | Szafranski, P. | Startek, M. | +2

102

Chromosome conformation capture-on-chip analysis of long-range cis-interactions of the SOX9 promoter

enthalten in: Chromosome research | 2013

von Smyk, M. | Szafranski, P. | Startek, M. | +2

103

Intragenic deletions of the IGF1 receptor gene in five individuals with psychiatric phenotypes and developmental delay

enthalten in: European journal of human genetics : EJHG | 2013

von Witsch, J. | Szafranski, P. | Chen, C. | +6

104

NAHR-mediated copy-number variants in a clinical population : mechanistic insights into both genomic disorders and Mendelizing traits

enthalten in: Genome research | 2013

von Dittwald, P. | Gambin, T. | Szafranski, P. | +25

105

NAHR-mediated copy-number variants in a clinical population: Mechanistic insights into both genomic disorders and Mendelizing traits

enthalten in: Genome research | 2013

von Dittwald, P. | Gambin, T. | Szafranski, P. | +25

106

Novel FOXF1 mutations in sporadic and familial cases of alveolar capillary dysplasia with misaligned pulmonary veins imply a role for its DNA binding domain

enthalten in: Human mutation | 2013

von Sen, P. | Yang, Y. | Navarro, C. | +79

107

Novel FOXF1 Mutations in Sporadic and Familial Cases of Alveolar Capillary Dysplasia with Misaligned Pulmonary Veins Imply a Role for its DNA Binding Domain

enthalten in: Human mutation | 2013

von Sen, P. | Yang, Y. | Navarro, C. | +79

108

Rare DNA copy number variants in cardiovascular malformations with extracardiac abnormalities

enthalten in: European journal of human genetics : EJHG | 2013

von Lalani, S. | Shaw, C. | Wang, X. | +25

109

Small noncoding differentially methylated copy-number variants, including lncRNA genes, cause a lethal lung developmental disorder

enthalten in: Genome research | 2013

von Szafranski, P. | Dharmadhikari, A. | Brosens, E. | +26

110

Small noncoding differentially methylated copy-number variants, including lncRNA genes, cause a lethal lung developmental disorder

enthalten in: Genome research | 2013

von Szafranski, P. | Dharmadhikari, A. | Brosens, E. | +26