Grossmann B - Search Results

1

Plasticity of human chromosome 3 during primate evolution.

Tsend-Ayush E, Grützner F, Yue Y, Grossmann B, Hänsel U, Sudbrak R, Haaf T. Tsend-Ayush E, et al. Among authors: grossmann b. Genomics. 2004 Feb;83(2):193-202. doi: 10.1016/j.ygeno.2003.08.012. Genomics. 2004. PMID: 14706448

2

Comparative cytogenetics of human chromosome 3q21.3 reveals a hot spot for ectopic recombination in hominoid evolution.

Yue Y, Grossmann B, Ferguson-Smith M, Yang F, Haaf T. Yue Y, et al. Among authors: grossmann b. Genomics. 2005 Jan;85(1):36-47. doi: 10.1016/j.ygeno.2004.10.007. Genomics. 2005. PMID: 15607420

3

Isolation and differential expression of two isoforms of the ROBO2/Robo2 axon guidance receptor gene in humans and mice.

Yue Y, Grossmann B, Galetzka D, Zechner U, Haaf T. Yue Y, et al. Among authors: grossmann b. Genomics. 2006 Dec;88(6):772-778. doi: 10.1016/j.ygeno.2006.05.011. Epub 2006 Jul 10. Genomics. 2006. PMID: 16829019 Free article.

4

De novo t(12;17)(p13.3;q21.3) translocation with a breakpoint near the 5' end of the HOXB gene cluster in a patient with developmental delay and skeletal malformations.

Yue Y, Farcas R, Thiel G, Bommer C, Grossmann B, Galetzka D, Kelbova C, Küpferling P, Daser A, Zechner U, Haaf T. Yue Y, et al. Among authors: grossmann b. Eur J Hum Genet. 2007 May;15(5):570-7. doi: 10.1038/sj.ejhg.5201795. Epub 2007 Feb 28. Eur J Hum Genet. 2007. PMID: 17327879

5

Homozygous disruption of PDZD7 by reciprocal translocation in a consanguineous family: a new member of the Usher syndrome protein interactome causing congenital hearing impairment.

Schneider E, Märker T, Daser A, Frey-Mahn G, Beyer V, Farcas R, Schneider-Rätzke B, Kohlschmidt N, Grossmann B, Bauss K, Napiontek U, Keilmann A, Bartsch O, Zechner U, Wolfrum U, Haaf T. Schneider E, et al. Among authors: grossmann b. Hum Mol Genet. 2009 Feb 15;18(4):655-66. doi: 10.1093/hmg/ddn395. Epub 2008 Nov 20. Hum Mol Genet. 2009. PMID: 19028668

6

A high oocyte yield for intracytoplasmic sperm injection treatment is associated with an increased chromosome error rate.

Haaf T, Hahn A, Lambrecht A, Grossmann B, Schwaab E, Khanaga O, Hahn T, Tresch A, Schorsch M. Haaf T, et al. Among authors: grossmann b. Fertil Steril. 2009 Mar;91(3):733-8. doi: 10.1016/j.fertnstert.2008.01.012. Epub 2008 Mar 7. Fertil Steril. 2009. PMID: 18314124 Free article.

7

Outcome of intracytoplasmic sperm injection with and without polar body diagnosis of oocytes.

Haaf T, Tresch A, Lambrecht A, Grossmann B, Schwaab E, Khanaga O, Hahn T, Schorsch M. Haaf T, et al. Among authors: grossmann b. Fertil Steril. 2010 Feb;93(2):405-15. doi: 10.1016/j.fertnstert.2009.02.064. Epub 2009 Apr 1. Fertil Steril. 2010. PMID: 19342037 Free article.

8

Conservation of the deleted-in-azoospermia-like-1 (DAZL1) gene structure in old world monkeys points to a homologous function of DAZL1 in this primate class.

Grossmann B, Weinbauer G, Hirschmann P, Vogt PH. Grossmann B, et al. J Endocrinol Invest. 2000 Oct;23(9):616-22. doi: 10.1007/BF03343785. J Endocrinol Invest. 2000. PMID: 11079458

9

Seborrhoische Keratosen.

Barthelmann S, Butsch F, Lang BM, Stege H, Großmann B, Schepler H, Grabbe S. Barthelmann S, et al. Among authors: grossmann b. J Dtsch Dermatol Ges. 2023 Mar;21(3):265-278. doi: 10.1111/ddg.14984_g. J Dtsch Dermatol Ges. 2023. PMID: 36929560

10

Seborrheic keratosis.

Barthelmann S, Butsch F, Lang BM, Stege H, Großmann B, Schepler H, Grabbe S. Barthelmann S, et al. Among authors: grossmann b. J Dtsch Dermatol Ges. 2023 Mar;21(3):265-277. doi: 10.1111/ddg.14984. Epub 2023 Mar 9. J Dtsch Dermatol Ges. 2023. PMID: 36892019 Review.

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