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Kalscheuer, V.
69  results:
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1

Hypergonadotropic hypogonadism in a patient with inv ins (2..:

Tzschach, A. ; Ramel, C. ; Kron, A....
International Journal of Andrology.  32 (2009)  3 - p. 226-230 , 2009
Link: https://doi.org/10.1111/..
 
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2

Eponymous Jacobsen syndrome: Mapping the breakpoints of the..:

Tümer, Z. ; Henriksen, A.M. ; Bache, I....
American Journal of Medical Genetics Part A.  140A (2006)  6 - p. 663-663 , 2006
Link: https://doi.org/10.1002/..
 
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3

Molecular characterization of a balanced chromosome translo..:

Tzschach, A ; Hoffmann, K ; Hoeltzenbein, M...
Clinical Genetics.  69 (2005)  2 - p. 189-193 , 2005
Link: https://doi.org/10.1111/..
 
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4

Divergent genetic and epigenetic post-zygotic isolation mec..:

Zechner, U. ; Shi, W. ; Hemberger, M....
Journal of Evolutionary Biology.  17 (2004)  2 - p. 453-460 , 2004
Link: https://doi.org/10.1046/..
 
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5

Delineation of an interstitial 9q22 deletion in basal cell ..:

Boonen, S.E. ; Stahl, D. ; Kreiborg, S....
American Journal of Medical Genetics Part A.  132A (2004)  3 - p. 324-328 , 2004
Link: https://doi.org/10.1002/..
 
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6

Prämature Ovarialinsuffizienz bei einer Patientin mit einem..:

Volleth, M. ; Stumm, M. ; Kalscheuer, V....
Geburtshilfe und Frauenheilkunde.  63 (2003)  10 - p. 1054-1057 , 2003
Link: https://doi.org/10.1055/..
 
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7

Biallelic Expression of the H19 and IGF2 Genes in Human Tes..:

van Gurp, R. J. H. L. M. ; Oosterhuis, J. W. ; Kalscheuer, V...
JNCI Journal of the National Cancer Institute.  86 (1994)  14 - p. 1070-1075 , 1994
Link: https://doi.org/10.1093/..
 
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8

Transcriptional activity of constitutive heterochromatin in..:

Sperling, K. ; Kalscheuer, V. ; Neitzel, H.
Experimental Cell Research.  173 (1987)  2 - p. 463-472 , 1987
Link: https://doi.org/10.1016/..
 
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9

The power of the Mediator complex—Expanding the genetic arc..:

Charzewska, A. ; Maiwald, R. ; Kahrizi, K....
Clinical Genetics.  94 (2018)  5 - p. 450-456 , 2018
Link: https://doi.org/10.1111/..
 
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10

HCFC1 loss-of-function mutations disrupt neuronal and neura..:

Jolly, L. A. ; Nguyen, L. S. ; Domingo, D....
Human Molecular Genetics.  24 (2015)  12 - p. 3335-3347 , 2015
Link: https://doi.org/10.1093/..
 
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11

New insights into Brunner syndrome and potential for target..:

Palmer, E.E. ; Leffler, M. ; Rogers, C....
Clinical Genetics.  89 (2015)  1 - p. 120-127 , 2015
Link: https://doi.org/10.1111/..
 
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12

In utero gene therapy rescues microcephaly caused by Pqbp1-..:

Ito, H ; Shiwaku, H ; Yoshida, C...
Molecular Psychiatry.  20 (2014)  4 - p. 459-471 , 2014
Link: https://doi.org/10.1038/..
 
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13

The X-chromosome-linked intellectual disability protein PQB..:

Kunde, S. A. ; Musante, L. ; Grimme, A....
Human Molecular Genetics.  20 (2011)  24 - p. 4916-4931 , 2011
Link: https://doi.org/10.1093/..
 
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14

Identification of candidate genes in patients with amyotrop..:

Dullinger, J.S ; Prudlo, J ; Roemer, K...
Aktuelle Neurologie.  32 (2005)  S 4 - p. , 2005
Link: https://doi.org/10.1055/..
 
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15

Molecular cytogenetic characterization of ring chromosome 1..:

Tümer, Z. ; Harboe, T.L. ; Blennow, E....
American Journal of Medical Genetics Part A.  130A (2004)  4 - p. 340-344 , 2004
Link: https://doi.org/10.1002/..
 
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