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M Nowaczyk

Showing results (161-170 of 216) with videos related to

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American Journal of Medical Genetics. Part A|February 14, 2006
Speech and language impairment and oromotor dyspraxia due to deletion of 7q31 that involves FOXP2Susan Zeesman, Małgorzata J M Nowaczyk, Ikuko Teshima, et al.
American Journal of Medical Genetics. Part A|January 19, 2008
Paternal deletion 6q24.3: a new congenital anomaly syndrome associated with intrauterine growth failure, early developmental delay and characteristic facial appearanceMałgorzata J M Nowaczyk, Melissa T Carter, Jie Xu, et al.
Physical Chemistry Chemical Physics : PCCP|February 15, 2014
Structure, ligands and substrate coordination of the oxygen-evolving complex of photosystem II in the S2 state: a combined EPR and DFT studyThomas Lohmiller, Vera Krewald, Montserrat Pérez Navarro, et al.
American Journal of Medical Genetics. Part A|June 29, 2012
Identification of a prenatal profile of Cornelia de Lange syndrome (CdLS): a review of 53 CdLS pregnanciesDinah M Clark, Ilana Sherer, Matthew A Deardorff, et al.
Journal of the American Society for Mass Spectrometry|June 27, 2022
Top-Down Identification and Sequence Analysis of Small Membrane Proteins Using MALDI-MS/MSJakob Meier-Credo, Laura Preiss, Imke Wüllenweber, et al.
Transplant International : Official Journal of the European Society for Organ Transplantation|January 1, 1994
Treatment of chronic hepatitis B and C with interferon-alpha in renal allograft recipients: preliminary resultsM Durlik, Z Rancewicz, Z Gaciong, et al.
Clinical Genetics|November 4, 2004
DHCR7 mutations and genotype-phenotype correlation in 37 Polish patients with Smith-Lemli-Opitz syndromeE Ciara, M J M Nowaczyk, M Witsch-Baumgartner, et al.
The Plant Cell|August 21, 2016
Thylakoid Membrane Architecture in <i>Synechocystis</i> Depends on CurT, a Homolog of the Granal CURVATURE THYLAKOID1 ProteinsSteffen Heinz, Anna Rast, Lin Shao, et al.
Clinical Genetics|February 3, 2006
Maternal urinary steroid profiles in prenatal diagnosis of Smith-Lemli-Opitz syndrome: first patient series comparing biochemical and molecular studiesA Jezela-Stanek, E M Małunowicz, E Ciara, et al.
Human Genetics|January 3, 2021
5q35 duplication presents with psychiatric and undergrowth phenotypes mediated by NSD1 overexpression and mTOR signaling downregulationFabiola Quintero-Rivera, Celeste C Eno, Christine Sutanto, et al.
Pageof 22

Showing results (161-170 of 216) with videos related to

Sort By:
Pageof 22
American Journal of Medical Genetics. Part A|February 14, 2006
Speech and language impairment and oromotor dyspraxia due to deletion of 7q31 that involves FOXP2Susan Zeesman, Małgorzata J M Nowaczyk, Ikuko Teshima, et al.
American Journal of Medical Genetics. Part A|January 19, 2008
Paternal deletion 6q24.3: a new congenital anomaly syndrome associated with intrauterine growth failure, early developmental delay and characteristic facial appearanceMałgorzata J M Nowaczyk, Melissa T Carter, Jie Xu, et al.
Physical Chemistry Chemical Physics : PCCP|February 15, 2014
Structure, ligands and substrate coordination of the oxygen-evolving complex of photosystem II in the S2 state: a combined EPR and DFT studyThomas Lohmiller, Vera Krewald, Montserrat Pérez Navarro, et al.
American Journal of Medical Genetics. Part A|June 29, 2012
Identification of a prenatal profile of Cornelia de Lange syndrome (CdLS): a review of 53 CdLS pregnanciesDinah M Clark, Ilana Sherer, Matthew A Deardorff, et al.
Journal of the American Society for Mass Spectrometry|June 27, 2022
Top-Down Identification and Sequence Analysis of Small Membrane Proteins Using MALDI-MS/MSJakob Meier-Credo, Laura Preiss, Imke Wüllenweber, et al.
Transplant International : Official Journal of the European Society for Organ Transplantation|January 1, 1994
Treatment of chronic hepatitis B and C with interferon-alpha in renal allograft recipients: preliminary resultsM Durlik, Z Rancewicz, Z Gaciong, et al.
Clinical Genetics|November 4, 2004
DHCR7 mutations and genotype-phenotype correlation in 37 Polish patients with Smith-Lemli-Opitz syndromeE Ciara, M J M Nowaczyk, M Witsch-Baumgartner, et al.
The Plant Cell|August 21, 2016
Thylakoid Membrane Architecture in <i>Synechocystis</i> Depends on CurT, a Homolog of the Granal CURVATURE THYLAKOID1 ProteinsSteffen Heinz, Anna Rast, Lin Shao, et al.
Clinical Genetics|February 3, 2006
Maternal urinary steroid profiles in prenatal diagnosis of Smith-Lemli-Opitz syndrome: first patient series comparing biochemical and molecular studiesA Jezela-Stanek, E M Małunowicz, E Ciara, et al.
Human Genetics|January 3, 2021
5q35 duplication presents with psychiatric and undergrowth phenotypes mediated by NSD1 overexpression and mTOR signaling downregulationFabiola Quintero-Rivera, Celeste C Eno, Christine Sutanto, et al.
Pageof 22