Suchergebnisse - "Eggermann, Thomas"

PubPharm (488)

71

Molecular testing for imprinting disorders

enthalten in: Medizinische Genetik | 2020

von Beygo, J. | Kanber, D. | Eggermann, T. | +1

72

Imprinting disorders: novel findings and translation into diagnostics and management

enthalten in: Medizinische Genetik | 2020

von Eggermann, T. | Horsthemke, B.

73

Clinical spectrum and management of imprinting disorders

enthalten in: Medizinische Genetik | 2020

von Elbracht, M. | Binder, G. | Hiort, O. | +3

74

Molecular testing for imprinting disorders

enthalten in: Medizinische Genetik | 2020

von Beygo, J. | Kanber, D. | Eggermann, T. | +1

75

Patient with an autosomal-recessive MBTPS1-linked phenotype and clinical features of Silver-Russell syndrome

enthalten in: American journal of medical genetics. Part A | 2020

von Meyer, R. | Elbracht, M. | Opladen, T. | +1

76

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 (Berlin, Germany) | 2020

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

77

Inherited cases of CNOT3-associated intellectual developmental disorder with speech delay, autism, and dysmorphic facies

enthalten in: Clinical genetics | 2020

von Meyer, R. | Begemann, M. | Demuth, S. | +9

78

Novel mutation points to a hot spot in CDKN1C causing Silver-Russell syndrome

enthalten in: Clinical epigenetics | 2020

von Binder, G. | Ziegler, J. | Schweizer, R. | +4

79

Novel mutation points to a hot spot in CDKN1C causing Silver–Russell syndrome

enthalten in: Clinical epigenetics | 2020

von Binder, G. | Ziegler, J. | Schweizer, R. | +4

80

Novel mutation points to a hot spot in CDKN1C causing Silver–Russell syndrome

enthalten in: Clinical epigenetics | 2020

von Binder, G. | Ziegler, J. | Schweizer, R. | +4