Liehr T - Search Results

1

Insulin-like growth factor type 1 deficiency in a Moroccan patient with de novo inverted duplication 9p24p12 and developmental delay: a case report.

Amasdl S, Natiq A, Elalaoui SC, Sbiti A, Liehr T, Sefiani A. Amasdl S, et al. Among authors: liehr t. J Med Case Rep. 2016 May 13;10(1):122. doi: 10.1186/s13256-016-0830-x. J Med Case Rep. 2016. PMID: 27178284 Free PMC article.

2

Characterization of a highly aberrant plasma cell leukemia karyotype: a case report.

Heller A, Fricke HJ, Starke H, Loncarevic IF, Claussen U, Liehr T. Heller A, et al. Among authors: liehr t. Oncol Rep. 2004 Jan;11(1):89-92. Oncol Rep. 2004. PMID: 14654908

3

Molecular cytogenetic characterization of a de novo supernumerary ring chromosome 7 resulting in partial trisomy, tetrasomy, and hexasomy in a child with dysmorphic signs, congenital heart defect, and developmental delay.

von Beust G, Sauter SM, Liehr T, Burfeind P, Bartels I, Starke H, von Eggeling F, Zoll B. von Beust G, et al. Among authors: liehr t. Am J Med Genet A. 2005 Aug 15;137(1):59-64. doi: 10.1002/ajmg.a.30835. Am J Med Genet A. 2005. PMID: 16007665 Review.

4

Three cases with rare interstitial rearrangements of chromosome 1 characterized by multicolor banding.

Polityko A, Starke H, Rumyantseva N, Claussen U, Liehr T, Raskin S. Polityko A, et al. Among authors: liehr t. Cytogenet Genome Res. 2005;111(2):171-4. doi: 10.1159/000086388. Cytogenet Genome Res. 2005. PMID: 16103660

5

Four small supernumerary marker chromosomes derived from chromosomes 6, 8, 11 and 12 in a patient with minimal clinical abnormalities: a case report.

Fernández-Toral J, Rodríguez L, Plasencia A, Martínez-Frías ML, Ewers E, Hamid AB, Ziegler M, Liehr T. Fernández-Toral J, et al. Among authors: liehr t. J Med Case Rep. 2010 Aug 3;4:239. doi: 10.1186/1752-1947-4-239. J Med Case Rep. 2010. PMID: 20682055 Free PMC article.

6

Characterization of a rare short arm heteromorphism of chromosome 22 in a girl with down-syndrome like facies.

Natiq A, Elalaoui SC, Liehr T, Amzazi S, Sefiani A. Natiq A, et al. Among authors: liehr t. Indian J Hum Genet. 2014 Jan;20(1):89-91. doi: 10.4103/0971-6866.132767. Indian J Hum Genet. 2014. PMID: 24959023 Free PMC article.

7

20p12.3 deletion is rare cause of syndromic cleft palate: case report and review of literature.

Amasdl S, Natiq A, Sbiti A, Zerkaoui M, Lyahyai J, Amzazi S, Liehr T, Sefiani A. Amasdl S, et al. Among authors: liehr t. BMC Res Notes. 2016 Jan 2;9:5. doi: 10.1186/s13104-015-1828-y. BMC Res Notes. 2016. PMID: 26724919 Free PMC article. Review.

8

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.

9

Childhood pre-B cell acute lymphoblastic leukemia with translocation t(1;19)(q21.1;p13.3) and two additional chromosomal aberrations involving chromosomes 1, 6, and 13: a case report.

Wafa A, As'sad M, Liehr T, Aljapawe A, Al Achkar W. Wafa A, et al. Among authors: liehr t. J Med Case Rep. 2017 Apr 7;11(1):94. doi: 10.1186/s13256-017-1251-1. J Med Case Rep. 2017. PMID: 28385156 Free PMC article.

10

Partial monosomy 8p and trisomy 16q in two children with developmental delay detected by array comparative genomic hybridization.

Papadopoulou Z, Papoulidis I, Sifakis S, Markopoulos G, Vetro A, Vlaikou AM, Ziegler M, Liehr T, Thomaidis L, Zuffardi O, Syrrou M, George K, Manolakos E. Papadopoulou Z, et al. Among authors: liehr t. Mol Med Rep. 2017 Dec;16(6):8808-8818. doi: 10.3892/mmr.2017.7760. Epub 2017 Oct 10. Mol Med Rep. 2017. PMID: 29039589 Free PMC article. Review.

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