Works matching IS 09365931 AND DT 2022 AND VI 34 AND IP 1

Results: 12

Newborn screening in Germany.

Published in:

2022

By:

Tönnies, Holger;
Nennstiel, Uta

Publication type:

Editorial

Jahresberichte 2021 aus den GfH-Kommissionen und GfH-Arbeitskreisen.

Published in:: Medizinische Genetik, 2022, v. 34, n. 1, p. 69, doi. 10.1515/medgen-2022-2118
Publication type:: Article

Second-tier strategies in newborn screening – potential and limitations.

Published in:

Medizinische Genetik, 2022, v. 34, n. 1, p. 21, doi. 10.1515/medgen-2022-2117

By:

Gramer, Gwendolyn;
Hoffmann, Georg F.

Publication type:

Article

Aktuelle Nachrichten.

Published in:: Medizinische Genetik, 2022, v. 34, n. 1, p. 89, doi. 10.1515/medgen-2022-2120
Publication type:: Article

Frontmatter.

Published in:: Medizinische Genetik, 2022, v. 34, n. 1, p. I, doi. 10.1515/medgen-2022-frontmatter1
Publication type:: Article

Über die Notwendigkeit der Anerkennung von sog. Kernberufsgruppen innerhalb der genetischen Gesundheitsversorgung in Europa.

Published in:

Medizinische Genetik, 2022, v. 34, n. 1, p. 81, doi. 10.1515/medgen-2022-2116

By:

Paneque, Milena;
Serra Juhé, Clara;
Melegh, Bela;
Carreira, Isabel;
Moog, Ute;
Liehr, Thomas

Publication type:

Article

Population-based screening in children for early diagnosis and treatment of familial hypercholesterolemia: design of the VRONI study.

Published in:

Medizinische Genetik, 2022, v. 34, n. 1, p. 41, doi. 10.1515/medgen-2022-2115

By:

Sanin, Veronika;
Schmieder, Raphael;
Ates, Sara;
Schlieben, Lea Dewi;
Wiehler, Jens;
Sun, Ruoyu;
Decker, Manuela;
Sander, Michaela;
Holdenrieder, Stefan;
Kohlmayer, Florian;
Friedmann, Anna;
Mall, Volker;
Feiler, Therese;
Dreßler, Arne;
Strom, Tim M.;
Prokisch, Holger;
Meitinger, Thomas;
von Scheidt, Moritz;
Koenig, Wolfgang;
Leipold, Georg

Publication type:

Article

Twenty years of newborn screening for congenital adrenal hyperplasia and congenital primary hypothyroidism – experiences from the DGKED/AQUAPE study group for quality improvement in Germany.

Published in:

Medizinische Genetik, 2022, v. 34, n. 1, p. 29, doi. 10.1515/medgen-2022-2114

By:

Hammersen, Johanna;
Bettendorf, Markus;
Bonfig, Walter;
Schönau, Eckhard;
Warncke, Katharina;
Eckert, Alexander J.;
Fricke-Otto, Susanne;
Palm, Katja;
Holl, Reinhard W.;
Woelfle, Joachim

Publication type:

Article

From newborn screening to genomic medicine: challenges and suggestions on how to incorporate genomic newborn screening in public health programs.

Published in:

Medizinische Genetik, 2022, v. 34, n. 1, p. 13, doi. 10.1515/medgen-2022-2113

By:

Dikow, Nicola;
Ditzen, Beate;
Kölker, Stefan;
Hoffmann, Georg F.;
Schaaf, Christian P.

Publication type:

Article

GenomDE und Modellvorhaben – neue Versorgungsstrukturen in der Humangenetik.

Published in:: Medizinische Genetik, 2022, v. 34, n. 1, p. 85, doi. 10.1515/medgen-2022-2111
Publication type:: Article

S1-Leitlinie: Tumorgenetik – Diagnostik im Kontext maligner Erkrankungen.

Published in:: Medizinische Genetik, 2022, v. 34, n. 1, p. 53, doi. 10.1515/medgen-2022-2112
Publication type:: Article

Legal aspects of newborn screening.

Published in:

Medizinische Genetik, 2022, v. 34, n. 1, p. 3, doi. 10.1515/medgen-2022-2110

By:

Rosenau, Henning;
Steffen, Felicia

Publication type:

Article