Suchergebnisse - "Kaulisch, Marc"

PubPharm (5)

1

FOXG1 syndrome : genotype-phenotype association in 83 patients with FOXG1 variants

enthalten in: Genetics in medicine : official journal of the American College of Medical Genetics | 2018

von Mitter, D. | Pringsheim, M. | Kaulisch, M. | +38

2

FOXG1 syndrome : genotype–phenotype association in 83 patients with FOXG1 variants

enthalten in: Genetics in medicine | 2018

von Mitter, D. | Pringsheim, M. | Kaulisch, M. | +38

3

Genotype-phenotype correlations in patients with retinoblastoma and interstitial 13q deletions

enthalten in: European journal of human genetics : EJHG | 2011

von Mitter, D. | Ullmann, R. | Muradyan, A. | +5

4

Loss at chromosome arm 16q in retinoblastoma : confirmation of the association with diffuse vitreous seeding and refinement of the recurrently deleted region

enthalten in: Genes, chromosomes & cancer | 2011

von Gustmann, S. | Klein-Hitpass, L. | Stephan, H. | +5

5

Loss at chromosome arm 16q in retinoblastoma: Confirmation of the association with diffuse vitreous seeding and refinement of the recurrently deleted region

enthalten in: Genes, chromosomes & cancer | 2011

von Gustmann, S. | Klein‐Hitpass, L. | Stephan, H. | +5

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