Revisiting the genotype‐phenotype correlation in children with medullary thyroid carcinoma: a report from the GPOH‐MET registry
- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- Umfang
-
Online-Ressource
- Sprache
-
Englisch
- Erschienen in
-
In: Pediatric Blood and Cancer, 67, 4, S. e28171-
- Ereignis
-
Veröffentlichung
- (wo)
-
Augsburg
- (wer)
-
Universität Augsburg
- (wann)
-
2020
- Ereignis
-
Veröffentlichung
- (wer)
-
Wiley
- (wann)
-
2020
- Urheber
- DOI
-
10.1002/pbc.28171
- URN
-
urn:nbn:de:bvb:384-opus4-773083
- Rechteinformation
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
- 14.08.2025, 08:55 UTC
Datenpartner
Dieses Objekt wird bereitgestellt von:
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Beteiligte
- Kuhlen, Michaela
- Frühwald, Michael
- Dunstheimer, Désirée Patricia Alexandra
- Vorwerk, Peter
- Redlich, Antje
- Universität Augsburg
- Wiley
Entstanden
- 2020
Ähnliche Objekte (12)
Revisiting the genotype‐phenotype correlation in children with medullary thyroid carcinoma : a report from the GPOH‐MET registry
Bridging molecular advancements and clinical challenges in pediatric oncology
Renal medullary carcinomas harbor a distinct methylation phenotype and display aberrant methylation of genes related to early nephrogenesis
Limbic encephalitis with LGI1 antibodies in a 14-year-old boy
PAX6 mutations: genotype-phenotype correlations
Genotype-phenotype correlations in FSHD
Genotype-phenotype: correlations and emerging spectrum
Genotype–phenotype correlations within the Geodermatophilaceae
BRD9 inhibition, alone or in combination with cytostatic compounds as a therapeutic approach in rhabdoid tumors
SWI/SNF-Komplex-assoziierte Tumordispositions-Syndrome
Non-malignant features of cancer predisposition syndromes manifesting in childhood and adolescence: a guide for the general pediatrician
Genotype–phenotype associations within the Li-Fraumeni spectrum: a report from the German Registry
Revisiting the genotype‐phenotype correlation in children with medullary thyroid carcinoma : a report from the GPOH‐MET registry
Bridging molecular advancements and clinical challenges in pediatric oncology
Renal medullary carcinomas harbor a distinct methylation phenotype and display aberrant methylation of genes related to early nephrogenesis
Limbic encephalitis with LGI1 antibodies in a 14-year-old boy
PAX6 mutations: genotype-phenotype correlations
Genotype-phenotype correlations in FSHD
Genotype-phenotype: correlations and emerging spectrum
Genotype–phenotype correlations within the Geodermatophilaceae
BRD9 inhibition, alone or in combination with cytostatic compounds as a therapeutic approach in rhabdoid tumors
SWI/SNF-Komplex-assoziierte Tumordispositions-Syndrome
Non-malignant features of cancer predisposition syndromes manifesting in childhood and adolescence: a guide for the general pediatrician
Genotype–phenotype associations within the Li-Fraumeni spectrum: a report from the German Registry
Revisiting the genotype‐phenotype correlation in children with medullary thyroid carcinoma : a report from the GPOH‐MET registry
Bridging molecular advancements and clinical challenges in pediatric oncology
Renal medullary carcinomas harbor a distinct methylation phenotype and display aberrant methylation of genes related to early nephrogenesis
Limbic encephalitis with LGI1 antibodies in a 14-year-old boy
PAX6 mutations: genotype-phenotype correlations
Genotype-phenotype correlations in FSHD
Genotype-phenotype: correlations and emerging spectrum
Genotype–phenotype correlations within the Geodermatophilaceae
BRD9 inhibition, alone or in combination with cytostatic compounds as a therapeutic approach in rhabdoid tumors
SWI/SNF-Komplex-assoziierte Tumordispositions-Syndrome
Non-malignant features of cancer predisposition syndromes manifesting in childhood and adolescence: a guide for the general pediatrician