G. Seidlitz
发表
F. Güttler,
K. Wulff,
F. Herrmann,
1988,
Clinical genetics.
K. Wulff,
F. Herrmann,
M. Schütz,
1989,
Prenatal diagnosis.
L. Platt,
M. Geraghty,
W. Rhead,
1999,
American journal of obstetrics and gynecology.
Carrier detection of Hunter syndrome (MPS II) by biochemical and DNA techniques in families at risk.
L. Petruschka,
J. Hopwood,
F. Herrmann,
1993,
Journal of medical genetics.
K. Wulff,
F. Herrmann,
M. Wehnert,
1994,
Human mutation.
C. P. Morris,
U. Pettersson,
J. Hopwood,
1992,
Human molecular genetics.
L. Petruschka,
M. Wehnert,
G. Seidlitz,
2004,
Human Genetics.
L. Petruschka,
J. Hopwood,
J. Bielicki,
1994,
Journal of Inherited Metabolic Disease.
F. Trefz,
K. Ullrich,
B. Fünders,
2009,
European Journal of Pediatrics.
P. Bührdel,
A. Naumann,
H. Böhme,
2005,
European Journal of Pediatrics.
H. Lauffer,
G. Hoffmann,
P. Lauenstein,
2015,
Neuropediatrics.
R. Wanders,
R. Schutgens,
C. Jakobs,
1990,
Journal of Inherited Metabolic Disease.
H. Lauffer,
P. Lauenstein,
G. Seidlitz,
2015,
Neuropediatrics.