Moog, Ute PD Dr. Dr. med.Universität HeidelbergHeidelberg
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- Rappold, Gudrun (7)
- Dikow, Nicola (7)
- Bartram, Claus R. (7)
- Kaufmann, Lilian Tamara (6)
- Sutter, Christian (6)
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- Freunscht, Inga (2)
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Recent publications in heiBIB 
(In total there are 68 publications catalogued)
- Paneque, Milena: Über die Notwendigkeit der Anerkennung von sog. Kernberufsgruppen innerhalb der genetischen Gesundheitsversorgung in Europa / Milena Paneque, Clara Serra Juhé, Bela Melegh, Isabel Carreira, Ute Moog und Thomas Liehr, 7. Mai 2022. - 3 S.
In: Medizinische Genetik, ISSN 1863-5490. 34(2022), 1, Seite 81-83
DOI: 10.1515/medgen-2022-2116
- Gieldon, Laura: Germ cell mosaicism for AUTS2 exon 6 deletion / Laura Gieldon, Anna Jauch, Katharina Obeid, Lilian Kaufmann, Katrin Hinderhofer, Ulrich Haug, Ute Mo… , 12 February 2021. - 5 S.
In: American journal of medical genetics, ISSN 1552-4833. 185(2021), 4, Seite 1261-1265
DOI: 10.1002/ajmg.a.62091
- Schwaibold, Eva: A boy with Silver-Russell syndrome and Sotos syndrome / Eva M.C. Schwaibold, Jasmin Beygo, Katharina Obeid, Anna Jauch, Katrin Hinderhofer, Ute Moog, 2021. - 6 S.
In: American journal of medical genetics, ISSN 1552-4833. 185(2021), 2, Seite 549-554
DOI: 10.1002/ajmg.a.61967
- Toberer, Ferdinand: Recurrent sebaceous carcinoma on the shoulder / Ferdinand Toberer, Ute Moog, Alexander Enk, Wolfgang Hartschuh, 10 January 2020. - 4 S.
In: Journal der Deutschen Dermatologischen Gesellschaft, ISSN 1610-0387. 18(2020), 3, Seite 247-250
DOI: 10.1111/ddg.14017
- Eßinger, Carla: Frequency of KCNQ1 variants causing loss of methylation of Imprinting Centre 2 in Beckwith-Wiedemann syndrome / Carla Eßinger, Stephanie Karch, Ute Moog, György Fekete, Anna Lengyel, Eva Pinti, Thomas Eggermann a… , 11 May 2020. - 7 S.
In: Clinical epigenetics, ISSN 1868-7083. 12(2020,1) Artikel-Nummer 63, 7 Seiten
DOI: 10.1186/s13148-020-00856-y
- Staufner, Christian: Defining clinical subgroups and genotype-phenotype correlations in NBAS-associated disease across 110 patients / Christian Staufner, MD, Bianca Peters, Matias Wagner, MD, Seham Alameer, MD, Ivo Barić, MD, PhD, Pie… , 2020. - 12 S.
In: Genetics in medicine, ISSN 1530-0366. 22(2020), 3, Seite 610-621
DOI: 10.1038/s41436-019-0698-4
- Harting, Inga: Oculodentodigital dysplasia : a hypomyelinating leukodystrophy with a characteristic MRI pattern of brain stem involvement / I. Harting, S. Karch, U. Moog, A. Seitz, P.J.W. Pouwels, and N.I. Wolf, 1 May 2019. - 5 S.
In: American journal of neuroradiology, ISSN 1936-959X. 40(2019), 5, Seite 903-907
DOI: 10.3174/ajnr.A6051
- Dikow, Nicola: What do parents expect from a genetic diagnosis of their child with intellectual disability? / Nicola Dikow, Ute Moog, Stephanie Karch, Anja Sander, Samuel Kilian, Rainer Blank, Gitta Reuner, 15 April 2019. - 9 S.
In: Journal of applied research in intellectual disabilities, ISSN 1468-3148. (2019), Seite 1-9
DOI: 10.1111/jar.12602
- Ott, Tim: The frog Xenopus as a model to study Joubert syndrome : the case of a human patient with compound heterozygous variants in PIBF1 / Tim Ott, Lilian Kaufmann, Martin Granzow, Katrin Hinderhofer, Claus R. Bartram, Susanne Theiß, Angel… , 25 February 2019. - 13 S.
In: Frontiers in physiology, ISSN 1664-042X. 10(2019) Artikel-Nummer 134, 13 Seiten
DOI: 10.3389/fphys.2019.00134
- Moog, Ute: An update on oculocerebrocutaneous (Delleman-Oorthuys) syndrome / Ute Moog, William B. Dobyns, 22 December 2018. - 9 S.
In: American journal of medical genetics, ISSN 1552-4876. 178(2018), 4, Seite 414-422
DOI: 10.1002/ajmg.c.31667
