Liehr T - Search Results

1

Premature ovarian failure caused by a heterozygous missense mutation in POF1B and a reciprocal translocation 46,X,t(X;3)(q21.1;q21.3).

Ledig S, Preisler-Adams S, Morlot S, Liehr T, Wieacker P. Ledig S, et al. Among authors: liehr t. Sex Dev. 2015;9(2):86-90. doi: 10.1159/000373906. Epub 2015 Feb 11. Sex Dev. 2015. PMID: 25676666

2

Incidental prenatal detection of an Xp deletion using an anonymous primer pair for fetal sexing.

Jakubiczka S, Mitulla B, Liehr T, Arnemann J, Lehrach H, Sudbrak R, Stumm M, Wieacker PF, Bettecken T. Jakubiczka S, et al. Among authors: liehr t. Prenat Diagn. 2000 Oct;20(10):842-6. doi: 10.1002/1097-0223(200010)20:10<842::aid-pd915>3.0.co;2-g. Prenat Diagn. 2000. PMID: 11038467

3

Genotype/phenotype analysis in a patient with pure and complete trisomy 12p.

Zumkeller W, Volleth M, Muschke P, Tönnies H, Heller A, Liehr T, Wieacker P, Stumm M. Zumkeller W, et al. Among authors: liehr t. Am J Med Genet A. 2004 Sep 1;129A(3):261-4. doi: 10.1002/ajmg.a.30125. Am J Med Genet A. 2004. PMID: 15326625

4

10p11.2 to 10q11.2 is a yet unreported region leading to unbalanced chromosomal abnormalities without phenotypic consequences.

Liehr T, Stumm M, Wegner RD, Bhatt S, Hickmann P, Patsalis PC, Meins M, Morlot S, Klaschka V, Ewers E, Hinreiner S, Mrasek K, Kosyakova N, Cai WW, Cheung SW, Weise A. Liehr T, et al. Cytogenet Genome Res. 2009;124(1):102-5. doi: 10.1159/000200094. Epub 2009 Apr 15. Cytogenet Genome Res. 2009. PMID: 19372675

5

8p23.1 duplication syndrome differentiated from copy number variation of the defensin cluster at prenatal diagnosis in four new families.

Barber JC, Bunyan D, Curtis M, Robinson D, Morlot S, Dermitzel A, Liehr T, Alves C, Trindade J, Paramos AI, Cooper C, Ocraft K, Taylor EJ, Maloney VK. Barber JC, et al. Among authors: liehr t. Mol Cytogenet. 2010 Feb 18;3:3. doi: 10.1186/1755-8166-3-3. Mol Cytogenet. 2010. PMID: 20167067 Free PMC article.

6

Five novel locations of Neocentromeres in human: 18q22.1, Xq27.1∼27.2, Acro p13, Acro p12, and heterochromatin of unknown origin.

Klein E, Rocchi M, Ovens-Raeder A, Kosyakova N, Weise A, Ziegler M, Meins M, Morlot S, Fischer W, Volleth M, Polityko A, Ogilvie CM, Kraus C, Liehr T. Klein E, et al. Among authors: liehr t. Cytogenet Genome Res. 2012;136(3):163-6. doi: 10.1159/000336648. Epub 2012 Mar 1. Cytogenet Genome Res. 2012. PMID: 22377933

7

A new multicolor fluorescence in situ hybridization probe set directed against human heterochromatin: HCM-FISH.

Bucksch M, Ziegler M, Kosayakova N, Mulatinho MV, Llerena JC Jr, Morlot S, Fischer W, Polityko AD, Kulpanovich AI, Petersen MB, Belitz B, Trifonov V, Weise A, Liehr T, Hamid AB. Bucksch M, et al. Among authors: liehr t. J Histochem Cytochem. 2012 Jul;60(7):530-6. doi: 10.1369/0022155412441708. Epub 2012 Apr 17. J Histochem Cytochem. 2012. PMID: 22511603 Free PMC article.

8

Human Ring Chromosomes - New Insights for their Clinical Significance.

Guilherme R, Klein E, Hamid A, Bhatt S, Volleth M, Polityko A, Kulpanovich A, Dufke A, Albrecht B, Morlot S, Brecevic L, Petersen M, Manolakos E, Kosyakova N, Liehr T. Guilherme R, et al. Among authors: liehr t. Balkan J Med Genet. 2013 Jun;16(1):13-20. doi: 10.2478/bjmg-2013-0013. Balkan J Med Genet. 2013. PMID: 24265580 Free PMC article.

9

Meiotic and sperm aneuploidy studies in three carriers of Robertsonian translocations and small supernumerary marker chromosomes.

Kirkpatrick G, Ren H, Liehr T, Chow V, Ma S. Kirkpatrick G, et al. Among authors: liehr t. Fertil Steril. 2015 May;103(5):1162-9.e7. doi: 10.1016/j.fertnstert.2015.02.006. Epub 2015 Mar 18. Fertil Steril. 2015. PMID: 25796321 Free article.

10

Acute promyelocytic leukemia with the translocation t(15;17)(q22;q21) associated with t(1;2)(q42~43;q11.2~12): a case report.

Wafa A, Moassass F, Liehr T, Al-Ablog A, Al-Achkar W. Wafa A, et al. Among authors: liehr t. J Med Case Rep. 2016 Jul 26;10:203. doi: 10.1186/s13256-016-0982-8. J Med Case Rep. 2016. PMID: 27459859 Free PMC article.

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