Suchergebnisse - "Eggermann, Thomas"

PubPharm (488)

81

Heterogeneous phenotypes in families with duplications of the paternal allele within the imprinting center 1 (H19/IGF2:TSS-DMR) in 11p15.5

enthalten in: Clinical genetics | 2020

von Eggermann, T. | Kraft, F. | Kloth, K. | +4

82

Cancer incidence and spectrum among children with genetically confirmed Beckwith-Wiedemann spectrum in Germany : a retrospective cohort study

enthalten in: British journal of cancer | 2020

von Cöktü, S. | Spix, C. | Kaiser, M. | +18

83

Need for a precise molecular diagnosis in Beckwith-Wiedemann and Silver-Russell syndrome: what has to be considered and why it is important

enthalten in: Journal of molecular medicine | 2020

von Eggermann, T. | Brück, J. | Knopp, C. | +7

84

Need for a precise molecular diagnosis in Beckwith-Wiedemann and Silver-Russell syndrome: what has to be considered and why it is important

enthalten in: Journal of molecular medicine | 2020

von Eggermann, T. | Brück, J. | Knopp, C. | +7

85

Need for a precise molecular diagnosis in Beckwith-Wiedemann and Silver-Russell syndrome: what has to be considered and why it is important

enthalten in: Journal of molecular medicine | 2020

von Eggermann, T. | Brück, J. | Knopp, C. | +7

86

HMGA2 Variants in Silver-Russell Syndrome : Homozygous and Heterozygous Occurrence

enthalten in: The Journal of clinical endocrinology and metabolism | 2020

von Hübner, C. | Meyer, R. | Kenawy, A. | +6

87

Genetic testing in inherited endocrine disorders : joint position paper of the European reference network on rare endocrine conditions (Endo-ERN)

enthalten in: Orphanet journal of rare diseases | 2020

von Eggermann, T. | Elbracht, M. | Kurth, I. | +110

88

Genetic testing in inherited endocrine disorders: joint position paper of the European reference network on rare endocrine conditions (Endo-ERN)

enthalten in: Orphanet journal of rare diseases | 2020

von Eggermann, T. | Elbracht, M. | Kurth, I. | +10

89

Genetic testing in inherited endocrine disorders: joint position paper of the European reference network on rare endocrine conditions (Endo-ERN)

enthalten in: Orphanet journal of rare diseases | 2020

von Eggermann, T. | Elbracht, M. | Kurth, I. | +10

90

upd(20)mat is a rare cause of the Silver-Russell-syndrome-like phenotype : Two unrelated cases and screening of large cohorts

enthalten in: Clinical genetics | 2020

von Hjortshøj, T. | Sørensen, A. | Yusibova, M. | +9