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Ute Moog

Showing results (21-30 of 79) with videos related to

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American Journal of Medical Genetics. Part A|November 16, 2020
A boy with Silver-Russell syndrome and Sotos syndromeEva M C Schwaibold, Jasmin Beygo, Katharina Obeid, et al.
American Journal of Medical Genetics. Part A|February 12, 2021
Germ cell mosaicism for AUTS2 exon 6 deletionLaura Gieldon, Anna Jauch, Katharina Obeid, et al.
American Journal of Medical Genetics. Part A|August 6, 2003
Chromosome bands and ends revisitedUte Moog, John J M Engelen, Connie T R M Schrander-Stumpel, et al.
Clinical Epigenetics|May 13, 2020
Frequency of KCNQ1 variants causing loss of methylation of Imprinting Centre 2 in Beckwith-Wiedemann syndromeCarla Eßinger, Stephanie Karch, Ute Moog, et al.
Familial Cancer|June 14, 2012
Hepatoblastoma in two siblings and familial adenomatous polyposis: causal nexus or coincidence?Christina Evers, Harald Gaspar, Matthias Kloor, et al.
European Journal of Human Genetics : EJHG|August 14, 2014
Characterization of the first intragenic SATB2 duplication in a girl with intellectual disability, nearly absent speech and suspected hypodontiaAnn-Sophie Kaiser, Bianca Maas, Anna Wolff, et al.
American Journal of Medical Genetics. Part A|November 16, 2007
Brain anomalies in encephalocraniocutaneous lipomatosisUte Moog, Marilyn C Jones, David H Viskochil, et al.
International Journal of Dermatology|November 15, 2008
Lymphedema-distichiasis syndrome: a distinct type of primary lymphedema caused by mutations in the FOXC2 geneMaaike Vreeburg, Martijn V Heitink, Robert J Damstra, et al.
European Journal of Human Genetics : EJHG|July 2, 2025
The European Certificate in Medical Genetics and Genomics (ECMGG)Peter D Turnpenny, Laura Pölsler, Ute Moog, et al.
Clinical Dysmorphology|January 7, 2003
Familial cryptic translocation with deletion 4q33-->4qter and duplication 7q34-->7qter in brothers with mental retardation, macrocephaly and iris colobomaUte Moog, John J M Engelen, Henny M J van Schrojenstein Lantman-de Valk, et al.
Pageof 8

Showing results (21-30 of 79) with videos related to

Sort By:
Pageof 8
American Journal of Medical Genetics. Part A|November 16, 2020
A boy with Silver-Russell syndrome and Sotos syndromeEva M C Schwaibold, Jasmin Beygo, Katharina Obeid, et al.
American Journal of Medical Genetics. Part A|February 12, 2021
Germ cell mosaicism for AUTS2 exon 6 deletionLaura Gieldon, Anna Jauch, Katharina Obeid, et al.
American Journal of Medical Genetics. Part A|August 6, 2003
Chromosome bands and ends revisitedUte Moog, John J M Engelen, Connie T R M Schrander-Stumpel, et al.
Clinical Epigenetics|May 13, 2020
Frequency of KCNQ1 variants causing loss of methylation of Imprinting Centre 2 in Beckwith-Wiedemann syndromeCarla Eßinger, Stephanie Karch, Ute Moog, et al.
Familial Cancer|June 14, 2012
Hepatoblastoma in two siblings and familial adenomatous polyposis: causal nexus or coincidence?Christina Evers, Harald Gaspar, Matthias Kloor, et al.
European Journal of Human Genetics : EJHG|August 14, 2014
Characterization of the first intragenic SATB2 duplication in a girl with intellectual disability, nearly absent speech and suspected hypodontiaAnn-Sophie Kaiser, Bianca Maas, Anna Wolff, et al.
American Journal of Medical Genetics. Part A|November 16, 2007
Brain anomalies in encephalocraniocutaneous lipomatosisUte Moog, Marilyn C Jones, David H Viskochil, et al.
International Journal of Dermatology|November 15, 2008
Lymphedema-distichiasis syndrome: a distinct type of primary lymphedema caused by mutations in the FOXC2 geneMaaike Vreeburg, Martijn V Heitink, Robert J Damstra, et al.
European Journal of Human Genetics : EJHG|July 2, 2025
The European Certificate in Medical Genetics and Genomics (ECMGG)Peter D Turnpenny, Laura Pölsler, Ute Moog, et al.
Clinical Dysmorphology|January 7, 2003
Familial cryptic translocation with deletion 4q33-->4qter and duplication 7q34-->7qter in brothers with mental retardation, macrocephaly and iris colobomaUte Moog, John J M Engelen, Henny M J van Schrojenstein Lantman-de Valk, et al.
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