Schmitt H - Search Results

1

Deletion mapping by FISH with BACs in patients with partial monosomy 22q13.

Schröder K, Schuffenhauer S, Seidel H, Bartsch O, Blin N, Hinkel GK, Schmitt H. Schröder K, et al. Among authors: schmitt h. Hum Genet. 1998 May;102(5):557-61. doi: 10.1007/s004390050739. Hum Genet. 1998. PMID: 9654204

2

Cloning of contiguous genomic fragments from human chromosome 21 harbouring three trefoil peptide genes.

Beck S, Schmitt H, Shizuya H, Blin N, Gött P. Beck S, et al. Among authors: schmitt h. Hum Genet. 1996 Aug;98(2):233-5. doi: 10.1007/s004390050198. Hum Genet. 1996. PMID: 8698350

3

A third P-domain peptide gene (TFF3), human intestinal trefoil factor, maps to 21q22.3.

Schmitt H, Wundrack I, Beck S, Gött P, Welter C, Shizuya H, Simon MI, Blin N. Schmitt H, et al. Cytogenet Cell Genet. 1996;72(4):299-302. doi: 10.1159/000134208. Cytogenet Cell Genet. 1996. PMID: 8641134

4

Cosmid-derived transcripts and sequence tags mapped to three subregions of human chromosome 22.

Pusch C, Müllenbach R, Gött P, Schmitt H, Wang Z, Roe B, Blin N. Pusch C, et al. Among authors: schmitt h. Gene. 1996 Dec 12;183(1-2):29-33. doi: 10.1016/s0378-1119(96)00411-8. Gene. 1996. PMID: 8996083

5

Human trefoil peptides: genomic structure in 21q22.3 and coordinated expression.

Gött P, Beck S, Machado JC, Carneiro F, Schmitt H, Blin N. Gött P, et al. Among authors: schmitt h. Eur J Hum Genet. 1996;4(6):308-15. doi: 10.1159/000472224. Eur J Hum Genet. 1996. PMID: 9043862

6

Classical and molecular cytogenetic methods in diagnosis of a rare translocation t(3;21).

Schmitt H, Sasiadek M, Jagielski J, Blin N. Schmitt H, et al. Int J Mol Med. 1998 Mar;1(3):569-71. doi: 10.3892/ijmm.1.3.569. Int J Mol Med. 1998. PMID: 9852264

7

Framework for a physical map of the human 22q13 region using bacterial artificial chromosomes (BACs).

Schmitt H, Kim UJ, Slepak T, Blin N, Simon MI, Shizuya H. Schmitt H, et al. Genomics. 1996 Apr 1;33(1):9-20. doi: 10.1006/geno.1996.0154. Genomics. 1996. PMID: 8617514

8

Telomere length variation in normal and malignant human tissues.

Schmitt H, Blin N, Zankl H, Scherthan H. Schmitt H, et al. Genes Chromosomes Cancer. 1994 Nov;11(3):171-7. doi: 10.1002/gcc.2870110306. Genes Chromosomes Cancer. 1994. PMID: 7530486

9

Involvement of 22q13.3 in chromosomal-anomalies.

Schmitt H, Kehrer H, Enders H, Latosbielenska A, Lamour V, Lipinski M, Blin N. Schmitt H, et al. Oncol Rep. 1994 Sep;1(5):881-4. doi: 10.3892/or.1.5.881. Oncol Rep. 1994. PMID: 21607459

10

Preservation of Murine Whole Eyes With Supplemented UW Cold Storage Solution: Anatomical Considerations.

Muench NA, Schmitt HM, Schlamp CL, Su AA, Washington K, Nickells RW. Muench NA, et al. Among authors: schmitt hm. Transl Vis Sci Technol. 2024 Nov 4;13(11):24. doi: 10.1167/tvst.13.11.24. Transl Vis Sci Technol. 2024. PMID: 39560629

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