Weise A - Search Results

1

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. Among authors: weise a. Front Genet. 2023 Dec 15;14:1293652. doi: 10.3389/fgene.2023.1293652. eCollection 2023. Front Genet. 2023. PMID: 38174048 Free PMC article.

2

Recombinant Chromosomes Resulting From Parental Pericentric Inversions-Two New Cases and a Review of the Literature.

Liehr T, Weise A, Mrasek K, Ziegler M, Padutsch N, Wilhelm K, Al-Rikabi A. Liehr T, et al. Among authors: weise a. Front Genet. 2019 Nov 14;10:1165. doi: 10.3389/fgene.2019.01165. eCollection 2019. Front Genet. 2019. PMID: 31798640 Free PMC article.

3

Frequency of small supernumerary marker chromosomes in prenatal, newborn, developmentally retarded and infertility diagnostics.

Liehr T, Weise A. Liehr T, et al. Among authors: weise a. Int J Mol Med. 2007 May;19(5):719-31. Int J Mol Med. 2007. PMID: 17390076

4

Chromosome 5 derived small supernumerary marker: towards a genotype/phenotype correlation of proximal chromosome 5 imbalances.

Melo JB, Backx L, Vermeesch JR, Santos HG, Sousa AC, Kosyakova N, Weise A, von Eggeling F, Liehr T, Carreira IM. Melo JB, et al. Among authors: weise a. J Appl Genet. 2011 May;52(2):193-200. doi: 10.1007/s13353-011-0035-3. Epub 2011 Mar 25. J Appl Genet. 2011. PMID: 21437654 Review.

5

Insertional translocation leading to a 4q13 duplication including the EPHA5 gene in two siblings with attention-deficit hyperactivity disorder.

Matoso E, Melo JB, Ferreira SI, Jardim A, Castelo TM, Weise A, Carreira IM. Matoso E, et al. Among authors: weise a. Am J Med Genet A. 2013 Aug;161A(8):1923-8. doi: 10.1002/ajmg.a.36032. Epub 2013 Jul 4. Am J Med Genet A. 2013. PMID: 23824631

6

Assessing Skewed X-Chromosome Inactivation.

Liehr T, Ziegler M, Löhmer S, Weise A. Liehr T, et al. Among authors: weise a. Curr Protoc Hum Genet. 2018 Jul;98(1):e66. doi: 10.1002/cphg.66. Epub 2018 Jul 10. Curr Protoc Hum Genet. 2018. PMID: 29989334

7

Small supernumerary marker chromosomes 1 with a normal phenotype.

Liehr T, Wegner RD, Stumm M, Martin T, Gillessen-Kaesbach G, Kosyakova N, Ewers E, Hamid AB, von Eggeling F, Hentschel J, Ziegler M, Weise A. Liehr T, et al. Among authors: weise a. J Chin Med Assoc. 2010 Apr;73(4):205-7. doi: 10.1016/S1726-4901(10)70042-3. J Chin Med Assoc. 2010. PMID: 20457442 Free article.

8

Overrepresentation of small supernumerary marker chromosomes (sSMC) from chromosome 6 origin in cases with multiple sSMC.

Liehr T, Starke H, Senger G, Melotte C, Weise A, Vermeesch JR. Liehr T, et al. Among authors: weise a. Am J Med Genet A. 2006 Jan 1;140(1):46-51. doi: 10.1002/ajmg.a.31048. Am J Med Genet A. 2006. PMID: 16333826 Review.

9

Handling small supernumerary marker chromosomes in prenatal diagnostics.

Liehr T, Ewers E, Kosyakova N, Klaschka V, Rietz F, Wagner R, Weise A. Liehr T, et al. Among authors: weise a. Expert Rev Mol Diagn. 2009 May;9(4):317-24. doi: 10.1586/erm.09.17. Expert Rev Mol Diagn. 2009. PMID: 19435454 Review.

10

A small supernumerary marker chromosome present in a Turner syndrome patient not derived from X- or Y-chromosome: a case report.

Sheth F, Ewers E, Kosyakova N, Weise A, Sheth J, Desai M, Andrieux J, Vermeesch J, Hamid AB, Ziegler M, Liehr T. Sheth F, et al. Among authors: weise a. Mol Cytogenet. 2009 Nov 12;2:22. doi: 10.1186/1755-8166-2-22. Mol Cytogenet. 2009. PMID: 19909521 Free PMC article.

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