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Silver-Russell syndrome is genetically opposite to ...Cell Press
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Nadine Schönherr. Nadine Schönherr. Affiliations. Institute of Human Genetics, RWTH Aachen, D Aachen, Germany. Search for articles by this author. DOI ... Nadine Schönherr. Nadine Schönherr. Affiliations. Institute of Human Genetics, RWTH Aachen, D Aachen, Germany. Search for articles by this author. DOI ...
A Mb Interstitial Deletion of 13q21 Without Phenotypic ...Wiley Online Library
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von A Roos · · Zitiert von: 12 — ... Nadine Schönherr,1. Thomas Eggermann,1 and Herdit M. Schüler1. 1Institute of Human Genetics, RWTH Aachen, Aachen, Germany. 2Institute of Molecular Biology ... von A Roos · · Zitiert von: 12 — ... Nadine Schönherr,1. Thomas Eggermann,1 and Herdit M. Schüler1. 1Institute of Human Genetics, RWTH Aachen, Aachen, Germany. 2Institute of Molecular Biology ...
Pure distal trisomy 2q: A rare chromosomal abnormality ...Wiley Online Library
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von M Elbracht · · Zitiert von: 13 — Nadine Schönherr,. Nadine Schönherr. Medical Faculty, Institute of Human Genetics, RWTH Aachen University, Aachen, Germany. Search for more ... von M Elbracht · · Zitiert von: 13 — Nadine Schönherr,. Nadine Schönherr. Medical Faculty, Institute of Human Genetics, RWTH Aachen University, Aachen, Germany. Search for more ...
Identification of a 21q22 duplication in a Silver–Russell ...Wiley Online Library
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— Nadine Schönherr,. Nadine Schönherr. Institute of Human Genetics, RWTH Aachen, Aachen, Germany. Search for more papers by this author · Sabrina — Nadine Schönherr,. Nadine Schönherr. Institute of Human Genetics, RWTH Aachen, Aachen, Germany. Search for more papers by this author · Sabrina ...
Broad Clinical Spectrum in Silver-Russell Syndrome and ...
publications.aap.org
von T Eggermann · · Zitiert von: 93 — Nadine Schönherr, MSc. aInstitute of Human Genetics, RWTH Aachen, Aachen, Germany. Search for other works by this author on:. › article...
A Mb interstitial deletion of 13q21 without phenotypic ...National Institutes of Health (NIH) (.gov)
pubmed.ncbi.nlm.nih.gov
von A Roos · · Zitiert von: 13 — Authors. Andreas Roos , Miriam Elbracht, Michael Baudis, Jan Senderek, Nadine Schönherr, Thomas Eggermann, Herdit M Schüler. Affiliation. 1 Institute ... von A Roos · · Zitiert von: 13 — Authors. Andreas Roos , Miriam Elbracht, Michael Baudis, Jan Senderek, Nadine Schönherr, Thomas Eggermann, Herdit M Schüler. Affiliation. 1 Institute ...
Broad clinical spectrum in Silver-Russell syndrome and ...National Institutes of Health (NIH) (.gov)
pubmed.ncbi.nlm.nih.gov
von T Eggermann · · Zitiert von: 96 — Nadine Schönherr. Affiliation. 1 Institute of Human GeneticsD Aachen, Germany. . PMID: ; DOI: peds ... von T Eggermann · · Zitiert von: 96 — Nadine Schönherr. Affiliation. 1 Institute of Human GeneticsD Aachen, Germany. . PMID: ; DOI: peds ...
Identification of a 21q22 duplication in a Silver-Russell ...National Institutes of Health (NIH) (.gov)
pubmed.ncbi.nlm.nih.gov
von T Eggermann · · Zitiert von: 24 — doi: ajmg.a Authors. Thomas Eggermann , Nadine Schönherr, ... von T Eggermann · · Zitiert von: 24 — doi: ajmg.a Authors. Thomas Eggermann , Nadine Schönherr, ...
Silver-Russell syndrome is genetically opposite to ...National Institutes of Health (NIH) (.gov)
pubmed.ncbi.nlm.nih.gov
von T Eggermann · · Zitiert von: 136 — Authors. Thomas Eggermann , Katja Eggermann, Nadine Schönherr. Affiliation. 1 Institute of Human Genetics, RWTH Aachen, Aachen, Germany. teggermann@ukaachen ... von T Eggermann · · Zitiert von: 136 — Authors. Thomas Eggermann , Katja Eggermann, Nadine Schönherr. Affiliation. 1 Institute of Human Genetics, RWTH Aachen, Aachen, Germany. teggermann@ukaachen ...
Broad Clinical Spectrum in Silver-Russell Syndrome and ...AAP
publications.aap.org
— Nadine Schönherr, MSc. Nadine Schönherr, MSc. aInstitute of Human Genetics, RWTH Aachen, Aachen, Germany. Search for other works by this author — Nadine Schönherr, MSc. Nadine Schönherr, MSc. aInstitute of Human Genetics, RWTH Aachen, Aachen, Germany. Search for other works by this author ...
Hypomethylation in the 11p15 telomeric imprinting domain ...National Institutes of Health (.gov)
pubmed.ncbi.nlm.nih.gov
von T Eggermann · · Zitiert von: 10 — Nadine Schönherr, Katja Eggermann, Hartmut Wollmann. PMID: ; PMCID: PMC ; DOI: jmg No abstract available. Publication types.
LOT1 (ZAC1/PLAGL1) as member of an imprinted gene ...National Institutes of Health (.gov)
pubmed.ncbi.nlm.nih.gov
von S Jäger · · Zitiert von: 7 — Nadine Schönherr, Sabrina Spengler, Michael B Ranke, Hartmut A Wollmann, Gerhard Binder, Thomas Eggermann. Affiliation. 1 Institute of Human Genetics, Aachen ...
Pure distal trisomy 2q: a rare chromosomal abnormality ...National Institutes of Health (NIH) (.gov)
pubmed.ncbi.nlm.nih.gov
von M Elbracht · · Zitiert von: 13 — Nadine Schönherr, Sabine Busse, Reinhild Damen, Klaus Zerres, Sabine Rudnik-Schöneborn, Herdit Monika Schüler. Affiliation. 1 Medical Faculty, Institute of ... von M Elbracht · · Zitiert von: 13 — Nadine Schönherr, Sabine Busse, Reinhild Damen, Klaus Zerres, Sabine Rudnik-Schöneborn, Herdit Monika Schüler. Affiliation. 1 Medical Faculty, Institute of ...
The centromeric 11p15 imprinting centre is also involved in...
pubmed.ncbi.nlm.nih.gov
Authors. Nadine Schönherr , Esther Meyer, Andreas Roos, Angela Schmidt, Hartmut A Wollmann, Thomas Eggermann. Affiliation. 1 Institute of Human Genetics, ...
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