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Kotzot, D
104
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Mediatypes
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1
Sustained response to brigatinib in a patient with refracto..:
Heregger, R.
;
Huemer, F.
;
Hutarew, G.
...
ESMO Open. 6 (2021) 4 - p. 100233 , 2021
Link:
https://doi.org/10.1016/..
?
2
ASPP2 deficiency causes features of 1q41q42 microdeletion s..:
Zak, J
;
Vives, V
;
Szumska, D
...
Cell Death & Differentiation. 23 (2016) 12 - p. 1973-1984 , 2016
Link:
https://doi.org/10.1038/..
?
3
Modification of risk for cancer as a coincidental finding i..:
Rostasy, K
;
Fauth, C
;
Gautsch, K
...
Clinical Genetics. 83 (2013) 3 - p. 284-287 , 2013
Link:
https://doi.org/10.1111/..
?
4
Chromosomal microaberrations in patients with epilepsy, int..:
Spreiz, A.
;
Haberlandt, E.
;
Baumann, M.
...
Clinical Genetics. 86 (2013) 4 - p. 361-366 , 2013
Link:
https://doi.org/10.1111/..
?
5
Medullary nephrocalcinosis in an adult patient with idiopat..:
Meusburger, E.
;
Mundlein, A.
;
Zitt, E.
...
Clinical Kidney Journal. 6 (2013) 2 - p. 211-215 , 2013
Link:
https://doi.org/10.1093/..
?
6
Parental origin of apparently balanced de novo complex chro..:
Grossmann, V
;
Höckner, M
;
Karmous‐Benailly, H
...
Clinical Genetics. 78 (2010) 6 - p. 548-553 , 2010
Link:
https://doi.org/10.1111/..
?
7
Hyperaminoaciduria and resolving phosphaturia in a family w..:
Köhle, J.K.
;
Kapelari, K.
;
Kotzot, D.
...
Bone. 45 (2009) - p. S93-S94 , 2009
Link:
https://doi.org/10.1016/..
?
8
Prenatal testing for uniparental disomy: indications and cl..:
Kotzot, D.
Ultrasound in Obstetrics & Gynecology. 31 (2007) 1 - p. 100-105 , 2007
Link:
https://doi.org/10.1002/..
?
9
Epigenetik und pädiatrische Krankheitsbilder:
Rittinger, O.
;
Kotzot, D.
Monatsschrift Kinderheilkunde. 153 (2005) 7 - p. 685-699 , 2005
Link:
https://doi.org/10.1007/..
?
10
Dizygotic twin boys born after ICSI with maternal meiosis I..:
Kotzot, D.
Human Reproduction. 17 (2002) 4 - p. 912-915 , 2002
Link:
https://doi.org/10.1093/..
?
11
A complex chromosome rearrangement involving chromosome 8, ..:
Kotzot, D
;
Holland, H
;
Köhler, M
.
Annales de Génétique. 44 (2001) 3 - p. 135-138 , 2001
Link:
https://doi.org/10.1016/..
?
12
Comparative analysis of isodisomic and heterodisomic segmen..:
Kotzot, D
Clinical Genetics. 60 (2001) 3 - p. 226-231 , 2001
Link:
https://doi.org/10.1034/..
?
13
Maternal uniparental disomy 7 - review and further delineat..:
Kotzot, D.
;
Balmer, D.
;
Baumer, A.
...
European Journal of Pediatrics. 159 (2000) 4 - p. 247-256 , 2000
Link:
https://doi.org/10.1007/..
?
14
No evidence of uniparental disomy 2, 6, 14, 16, 20, and 22 ..:
Kotzot, D
;
Lurie, IW
;
Méhes, K
..
Clinical Genetics. 58 (2000) 3 - p. 177-180 , 2000
Link:
https://doi.org/10.1034/..
?
15
Delineation of 7q11.2 Deletions Associated with Williams–Be..:
Robinson, W.P.
;
Waslynka, J.
;
Bernasconi, F.
...
Genomics. 34 (1996) 1 - p. 17-23 , 1996
Link:
https://doi.org/10.1006/..
1-15