Muenke M - Search Results

1

Loss of chromosome 8p sequences in human breast carcinoma cell lines.

Pykett MJ, Murphy ME, Harnish PR, Muenke M, Marks J, George DL. Pykett MJ, et al. Among authors: muenke m. Cancer Genet Cytogenet. 1994 Aug;76(1):23-8. doi: 10.1016/0165-4608(94)90064-7. Cancer Genet Cytogenet. 1994. PMID: 8076345

2

Cytogenetic rearrangements involving the loss of the Sonic Hedgehog gene at 7q36 cause holoprosencephaly.

Roessler E, Ward DE, Gaudenz K, Belloni E, Scherer SW, Donnai D, Siegel-Bartelt J, Tsui LC, Muenke M. Roessler E, et al. Among authors: muenke m. Hum Genet. 1997 Aug;100(2):172-81. doi: 10.1007/s004390050486. Hum Genet. 1997. PMID: 9254845

3

The genomic structure, chromosome location, and analysis of the human DKK1 head inducer gene as a candidate for holoprosencephaly.

Roessler E, Du Y, Glinka A, Dutra A, Niehrs C, Muenke M. Roessler E, et al. Among authors: muenke m. Cytogenet Cell Genet. 2000;89(3-4):220-4. doi: 10.1159/000015618. Cytogenet Cell Genet. 2000. PMID: 10965128

4

Molecular characterization of breakpoints in patients with holoprosencephaly and definition of the HPE2 critical region 2p21.

Schell U, Wienberg J, Köhler A, Bray-Ward P, Ward DE, Wilson WG, Allen WP, Lebel RR, Sawyer JR, Campbell PL, Aughton DJ, Punnett HH, Lammer EJ, Kao FT, Ward DC, Muenke M. Schell U, et al. Among authors: muenke m. Hum Mol Genet. 1996 Feb;5(2):223-9. doi: 10.1093/hmg/5.2.223. Hum Mol Genet. 1996. PMID: 8824878

5

Physical mapping of the holoprosencephaly critical region in 18p11.3.

Overhauser J, Mitchell HF, Zackai EH, Tick DB, Rojas K, Muenke M. Overhauser J, et al. Among authors: muenke m. Am J Hum Genet. 1995 Nov;57(5):1080-5. Am J Hum Genet. 1995. PMID: 7485158 Free PMC article.

6

A common mutation in the fibroblast growth factor receptor 1 gene in Pfeiffer syndrome.

Muenke M, Schell U, Hehr A, Robin NH, Losken HW, Schinzel A, Pulleyn LJ, Rutland P, Reardon W, Malcolm S, et al. Muenke M, et al. Nat Genet. 1994 Nov;8(3):269-74. doi: 10.1038/ng1194-269. Nat Genet. 1994. PMID: 7874169

7

Regional assignment of the human homeobox-containing gene EN1 to chromosome 2q13-q21.

Köhler A, Logan C, Joyner AL, Muenke M. Köhler A, et al. Among authors: muenke m. Genomics. 1993 Jan;15(1):233-5. doi: 10.1006/geno.1993.1045. Genomics. 1993. PMID: 8094370 Free article.

8

A gene for cleidocranial dysplasia maps to the short arm of chromosome 6.

Feldman GJ, Robin NH, Brueton LA, Robertson E, Thompson EM, Siegel-Bartelt J, Gasser DL, Bailey LC, Zackai EH, Muenke M. Feldman GJ, et al. Among authors: muenke m. Am J Hum Genet. 1995 Apr;56(4):938-43. Am J Hum Genet. 1995. PMID: 7717404 Free PMC article.

9

Structure of the human gene encoding the associated microfibrillar protein (MFAP1) and localization to chromosome 15q15-q21.

Yeh H, Chow M, Abrams WR, Fan J, Foster J, Mitchell H, Muenke M, Rosenbloom J. Yeh H, et al. Among authors: muenke m. Genomics. 1994 Sep 15;23(2):443-9. doi: 10.1006/geno.1994.1521. Genomics. 1994. PMID: 7835894 Free article.

10

Molecular analysis of the 18q- syndrome--and correlation with phenotype.

Kline AD, White ME, Wapner R, Rojas K, Biesecker LG, Kamholz J, Zackai EH, Muenke M, Scott CI Jr, Overhauser J. Kline AD, et al. Among authors: muenke m. Am J Hum Genet. 1993 May;52(5):895-906. Am J Hum Genet. 1993. PMID: 8488839 Free PMC article. Review.

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