Sevjidmaa Baasanjav

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

P. Robinson, R. Fahsold, L. Graul-Neumann, 2010, American journal of medical genetics. Part A.

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

S. Mundlos, I. Demuth, S. Mansour, 2010, Nucleus.

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

D. Horn, S. Mundlos, A. Latos-Bieleńska, 2010, BMC Medical Genetics.

Faulty initiation of proteoglycan synthesis causes cardiac and joint defects.

D. Seelow, D. Horn, S. Mundlos, 2011, American journal of human genetics.

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

S. Mundlos, I. Demuth, S. Mansour, 2010, Nucleus.