Title |
One test for all: whole exome sequencing significantly improves the diagnostic yield in growth retarded patients referred for molecular testing for Silver–Russell syndrome |
|---|---|
Involved |
Robert Meyer (Verfasser)
Matthias Begemann (Verfasser) Christian Thomas Hübner (Verfasser) Daniela Dey (Verfasser)
Alma Kuechler (Verfasser)
Magdeldin Elgizouli (Verfasser) Ulrike Schara (Verfasser) Laima Ambrozaityte (Verfasser) Birute Burnyte (Verfasser) Carmen Schröder (Verfasser) Asmaa Kenawy (Verfasser) Peter Kroisel (Verfasser) Stephanie Demuth (Verfasser) Gyorgy Fekete (Verfasser) Thomas Opladen (Verfasser) Miriam Elbracht (Verfasser) Thomas Eggermann (Verfasser) SpringerLink (Online service) (Sonstige) |
Published in |
Orphanet journal of rare diseases : OJRD 16, 1, 22.1.2021, date:12.2021, Seite 1-10 |
Published |
2021 |
Language |
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Country |
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Topic |
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Subject |
Medicine/Public Health, general. |
DDC notation |
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Persistent identifier |
urn:nbn:de:101:1-2021031418133869920048 (URN) |
Record ID |
1229329234 |
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