Suchergebnisse - "Bayram, Yavuz"

PubPharm (3)

1

Exome sequencing reveals homozygous TRIM2 mutation in a patient with early onset CMT and bilateral vocal cord paralysis

enthalten in: Human genetics | 2015

von Pehlivan, D. | Coban Akdemir, Z. | Karaca, E. | +9

2

Exome sequencing reveals homozygous TRIM2 mutation in a patient with early onset CMT and bilateral vocal cord paralysis

enthalten in: Human genetics | 2015

von Pehlivan, D. | Coban Akdemir, Z. | Karaca, E. | +9

3

Exome sequencing reveals homozygous TRIM2 mutation in a patient with early onset CMT and bilateral vocal cord paralysis

enthalten in: Human genetics | 2015

von Pehlivan, D. | Coban Akdemir, Z. | Karaca, E. | +9

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