Liehr T - Search Results

1

Über die Notwendigkeit der Anerkennung von sog. Kernberufsgruppen innerhalb der genetischen Gesundheitsversorgung in Europa.

Paneque M, Serra Juhé C, Melegh B, Carreira I, Moog U, Liehr T. Paneque M, et al. Among authors: liehr t. Med Genet. 2022 May 7;34(1):81-83. doi: 10.1515/medgen-2022-2116. eCollection 2022 Apr. Med Genet. 2022. PMID: 38836018 Free PMC article. German. No abstract available.

2

Small supernumerary marker chromosomes derived from human chromosome 11.

Liehr T, Ziegler M, Person L, Kankel S, Padutsch N, Weise A, Weimer JP, Williams H, Ferreira S, Melo JB, Carreira IM. Liehr T, et al. Front Genet. 2023 Dec 15;14:1293652. doi: 10.3389/fgene.2023.1293652. eCollection 2023. Front Genet. 2023. PMID: 38174048 Free PMC article.

3

Erratum zu: Über die Notwendigkeit der Anerkennung von sog. Kernberufsgruppen innerhalb der genetischen Gesundheitsversorgung in Europa.

Paneque M, Serra Juhé C, Melegh B, Carreira I, Moog U, Liehr T. Paneque M, et al. Among authors: liehr t. Med Genet. 2022 Jun 4;34(2):189-191. doi: 10.1515/medgen-2022-2122. eCollection 2022 Jun. Med Genet. 2022. PMID: 38835907 Free PMC article. German.

4

Editorial: Co-occurrence of numerical and structural aberration-small supernumerary marker chromosomes and B-chromosomes.

Liehr T. Liehr T. Front Genet. 2024 Apr 17;15:1408674. doi: 10.3389/fgene.2024.1408674. eCollection 2024. Front Genet. 2024. PMID: 38699228 Free PMC article. No abstract available.

5

Joubert syndrome: Molecular basis and treatment.

Spahiu L, Behluli E, Grajçevci-Uka V, Liehr T, Temaj G. Spahiu L, et al. Among authors: liehr t. J Mother Child. 2023 Feb 22;26(1):118-123. doi: 10.34763/jmotherandchild.20222601.d-22-00034. eCollection 2022 Mar 1. J Mother Child. 2023. PMID: 36803942 Free PMC article. Review.

6

Noninvasive prenatal testing (NIPT) results are less accurate the later applied during pregnancy.

Liehr T. Liehr T. Taiwan J Obstet Gynecol. 2024 Nov;63(6):892-895. doi: 10.1016/j.tjog.2024.05.027. Taiwan J Obstet Gynecol. 2024. PMID: 39481998 Free article. Review.

7

A maternally derived complex small supernumerary marker chromosome involving chromosomes 8 and 14: case report and review of the literature.

Ouboukss F, El Amrani Z, Bouchahta H, Ratbi I, Sbiti A, Liehr T, Sefiani A, Natiq A. Ouboukss F, et al. Among authors: liehr t. Front Genet. 2024 Feb 23;15:1331676. doi: 10.3389/fgene.2024.1331676. eCollection 2024. Front Genet. 2024. PMID: 38463166 Free PMC article.

8

Currarino Syndrome in Two Moroccan Siblings with Inherited 7q36 Deletion due to Maternal t(7;21)(q36;p11)mat: A Case Report.

El Amrani Z, Natiq A, Sbiti A, Ratbi I, Liehr T, Sefiani A, Sahli M. El Amrani Z, et al. Among authors: liehr t. Mol Syndromol. 2024 Mar;15(2):125-129. doi: 10.1159/000534432. Epub 2023 Nov 3. Mol Syndromol. 2024. PMID: 38585544 Free PMC article.

9

CHD2 pathogenic nonsense variant in a three-generation family with variable phenotype and a paracentric inversion 16: Case report.

Angelopoulou E, Theodosiou A, Papaevripidou I, Alexandrou A, Liehr T, Gyftodimou Y, Stefanou EG, Sismani C. Angelopoulou E, et al. Among authors: liehr t. Heliyon. 2023 Nov 28;9(12):e22987. doi: 10.1016/j.heliyon.2023.e22987. eCollection 2023 Dec. Heliyon. 2023. PMID: 38125503 Free PMC article.

10

Mucopolysaccharidosis type III (subtype IIIB) diagnosis as a spectrum disorder: A case report from Kosovo.

Spahiu L, Behluli E, Hadziselimovic R, Liehr T, Temaj G. Spahiu L, et al. Among authors: liehr t. Folia Med (Plovdiv). 2023 Feb 28;65(1):161-165. doi: 10.3897/folmed.65.e70924. Folia Med (Plovdiv). 2023. PMID: 36855989

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