Suchergebnisse - "Baasanjav, Sevjidmaa"

PubPharm (12)

1

Unilateral Multifocal Inner Ear and Internal Auditory Canal or Cerebellopontine Angle Cochleovestibular Schwannomas-Genetic Analysis and Management by Surgical Resection and Cochlear Implantation

enthalten in: Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology | 2024

von Plontke, S. | Hoffmann, K. | Caye-Thomasen, P. | +9

2

Identifizierung und Charakterisierung genetischer Ursachen von Skelettdysplasien

Erschienen: 2014

von Baasanjav, S.

3

Faulty initiation of proteoglycan synthesis causes cardiac and joint defects

enthalten in: American journal of human genetics | 2011

von Baasanjav, S. | Al-Gazali, L. | Hashiguchi, T. | +20

4

Faulty Initiation of Proteoglycan Synthesis Causes Cardiac and Joint Defects

enthalten in: American journal of human genetics | 2011

von Baasanjav, S. | Al-Gazali, L. | Hashiguchi, T. | +20

5

Marfan syndrome with neonatal progeroid syndrome-like lipodystrophy associated with a novel frameshift mutation at the 3' terminus of the FBN1-gene

enthalten in: American journal of medical genetics. Part A | 2010

von Graul-Neumann, L. | Kienitz, T. | Robinson, P. | +7

6

Mutations causing Greenberg dysplasia but not Pelger anomaly uncouple enzymatic from structural functions of a nuclear membrane protein

enthalten in: Nucleus (Austin, Tex.) | 2010

von Clayton, P. | Fischer, B. | Mann, A. | +18

7

Osteopoikilosis and multiple exostoses caused by novel mutations in LEMD3 and EXT1 genes respectively--coincidence within one family

enthalten in: BMC medical genetics | 2010

von Baasanjav, S. | Jamsheer, A. | Kolanczyk, M. | +5

8

Osteopoikilosis and multiple exostoses caused by novel mutations in LEMD3 and EXT1 genes respectively - coincidence within one family

enthalten in: BMC medical genetics | 2010

von Baasanjav, S. | Jamsheer, A. | Kolanczyk, M. | +5

9

Osteopoikilosis and multiple exostoses caused by novel mutations in LEMD3 and EXT1 genes respectively - coincidence within one family

enthalten in: BMC medical genetics | 2010

von Baasanjav, S. | Jamsheer, A. | Kolanczyk, M. | +5

10

Osteopoikilosis and multiple exostoses caused by novel mutations in LEMD3 and EXT1 genes respectively - coincidence within one family

in: BMC medical genetics | 2010

von Baasanjav, S. | Jamsheer, A. | Kolanczyk, M. | +5