Muenke M - Search Results

1

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

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

Holoprosencephaly: molecular study of a California population.

Nanni L, Croen LA, Lammer EJ, Muenke M. Nanni L, et al. Among authors: muenke m. Am J Med Genet. 2000 Feb 14;90(4):315-9. doi: 10.1002/(sici)1096-8628(20000214)90:4<315::aid-ajmg10>3.0.co;2-y. Am J Med Genet. 2000. PMID: 10710230

4

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.

5

Fibroblast-growth-factor receptor mutations in human skeletal disorders.

Muenke M, Schell U. Muenke M, et al. Trends Genet. 1995 Aug;11(8):308-13. doi: 10.1016/s0168-9525(00)89088-5. Trends Genet. 1995. PMID: 8585128 Free article. Review.

6

A region-specific microdissection library for human chromosome 2p23-->p21 and the analysis of an interstitial deletion of 2p21.

Kao FT, Yu J, Qi J, Tong S, Muenke M. Kao FT, et al. Among authors: muenke m. Cytogenet Cell Genet. 1995;68(1-2):17-8. doi: 10.1159/000133880. Cytogenet Cell Genet. 1995. PMID: 7956351

7

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.

8

Sub-band deletion of 7q36.3 in a patient with ring chromosome 7: association with holoprosencephaly.

Sawyer JR, Lukacs JL, Hassed SJ, Arnold GL, Mitchell HF, Muenke M. Sawyer JR, et al. Among authors: muenke m. Am J Med Genet. 1996 Oct 16;65(2):113-6. doi: 10.1002/(SICI)1096-8628(19961016)65:2<113::AID-AJMG6>3.0.CO;2-T. Am J Med Genet. 1996. PMID: 8911601

9

A novel phenotypic pattern in X-linked inheritance: craniofrontonasal syndrome maps to Xp22.

Feldman GJ, Ward DE, Lajeunie-Renier E, Saavedra D, Robin NH, Proud V, Robb LJ, Der Kaloustian V, Carey JC, Cohen MM Jr, Cormier V, Munnich A, Zackai EH, Wilkie AO, Price RA, Muenke M. Feldman GJ, et al. Among authors: muenke m. Hum Mol Genet. 1997 Oct;6(11):1937-41. doi: 10.1093/hmg/6.11.1937. Hum Mol Genet. 1997. PMID: 9302274

10

Physical mapping of the holoprosencephaly critical region in 21q22.3, exclusion of SIM2 as a candidate gene for holoprosencephaly, and mapping of SIM2 to a region of chromosome 21 important for Down syndrome.

Muenke M, Bone LJ, Mitchell HF, Hart I, Walton K, Hall-Johnson K, Ippel EF, Dietz-Band J, Kvaløy K, Fan CM, et al. Muenke M, et al. Am J Hum Genet. 1995 Nov;57(5):1074-9. Am J Hum Genet. 1995. PMID: 7485157 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

326 results

Search Page

Filters