C. Schrander‐Stumpel
发表
J. Fryns,
L. Curfs,
S. Cassidy,
2004,
American journal of medical genetics. Part A.
E. Smeets,
M. Vreeburg,
M. V. van Steensel,
2008,
International journal of dermatology.
J. Al-Aama,
J. Opitz,
W. Reardon,
2012,
European Journal of Human Genetics.
H. Smeets,
A. Paulussen,
A. Haeringen,
2010,
European Journal of Human Genetics.
M. V. van Steensel,
C. Schrander‐Stumpel,
L. Parren,
2008,
Experimental dermatology.
M. Sinnema,
L. Curfs,
M. Maaskant,
2007,
American journal of medical genetics. Part C, Seminars in medical genetics.
J. Fryns,
B. Hamel,
M. Krom,
1993,
Clinical genetics.
L. Curfs,
C. Schrander‐Stumpel,
J. Schrander,
2005,
American journal of medical genetics. Part A.
K. Devriendt,
J. Vermeesch,
J. Fryns,
2009,
BMJ Case Reports.
K. Devriendt,
J. Vermeesch,
J. Fryns,
2007,
Journal of Medical Genetics.
Paul Coucke,
Marjolijn Renard,
Bart Loeys,
2013,
International journal of cardiology.
REEP1 mutation spectrum and genotype/phenotype correlation in hereditary spastic paraplegia type 31.
M. Pericak-Vance,
H. Smeets,
S. Züchner,
2008,
Brain : a journal of neurology.
H. Smeets,
T. de Ravel,
K. Devriendt,
2011,
Human mutation.
J. Al-Aama,
J. Opitz,
W. Reardon,
2012,
American journal of medical genetics. Part A.
J. Schrander,
J. Engelen,
L. Spruijt,
2004,
American journal of medical genetics. Part A.
C. Schrander‐Stumpel,
C. Schrander-Stumpel,
Connie Schrander-Stumpel,
1999,
American journal of medical genetics.
J. Fryns,
J. Engelen,
C. Schrander‐Stumpel,
1994,
Clinical genetics.
C. Cytrynbaum,
C. Marshall,
A. Noor,
2015,
Clinical genetics.