Pressman CL - Search Results

1

Molecular analysis of chromosome 9q deletions in two Gorlin syndrome patients.

Shimkets R, Gailani MR, Siu VM, Yang-Feng T, Pressman CL, Levanat S, Goldstein A, Dean M, Bale AE. Shimkets R, et al. Among authors: pressman cl. Am J Hum Genet. 1996 Aug;59(2):417-22. Am J Hum Genet. 1996. PMID: 8755929 Free PMC article.

2

The role of the human homologue of Drosophila patched in sporadic basal cell carcinomas.

Gailani MR, Ståhle-Bäckdahl M, Leffell DJ, Glynn M, Zaphiropoulos PG, Pressman C, Undén AB, Dean M, Brash DE, Bale AE, Toftgård R. Gailani MR, et al. Nat Genet. 1996 Sep;14(1):78-81. doi: 10.1038/ng0996-78. Nat Genet. 1996. PMID: 8782823

3

Pulsed-field gel electrophoresis and FISH mapping of chromosome 9q22: placement of a novel zinc finger gene within the NBCCS and ESS1 region.

Levanat S, Chidambaram A, Wicking C, Bray-Ward P, Pressman C, Toftgard R, Gailani MR, Myers JC, Wainwright B, Dean M, Bale AE. Levanat S, et al. Cytogenet Cell Genet. 1997;76(3-4):208-13. doi: 10.1159/000134551. Cytogenet Cell Genet. 1997. PMID: 9186526

4

Mutations of the human homolog of Drosophila patched in the nevoid basal cell carcinoma syndrome.

Hahn H, Wicking C, Zaphiropoulous PG, Gailani MR, Shanley S, Chidambaram A, Vorechovsky I, Holmberg E, Unden AB, Gillies S, Negus K, Smyth I, Pressman C, Leffell DJ, Gerrard B, Goldstein AM, Dean M, Toftgard R, Chenevix-Trench G, Wainwright B, Bale AE. Hahn H, et al. Cell. 1996 Jun 14;85(6):841-51. doi: 10.1016/s0092-8674(00)81268-4. Cell. 1996. PMID: 8681379 Free article.

5

Function of Rieger syndrome gene in left-right asymmetry and craniofacial development.

Lu MF, Pressman C, Dyer R, Johnson RL, Martin JF. Lu MF, et al. Nature. 1999 Sep 16;401(6750):276-8. doi: 10.1038/45797. Nature. 1999. PMID: 10499585

6

Multiple calvarial defects in lmx1b mutant mice.

Chen H, Ovchinnikov D, Pressman CL, Aulehla A, Lun Y, Johnson RL. Chen H, et al. Among authors: pressman cl. Dev Genet. 1998;22(4):314-20. doi: 10.1002/(SICI)1520-6408(1998)22:4<314::AID-DVG2>3.0.CO;2-9. Dev Genet. 1998. PMID: 9664684

7

LMX1B, a LIM homeodomain class transcription factor, is necessary for normal development of multiple tissues in the anterior segment of the murine eye.

Pressman CL, Chen H, Johnson RL. Pressman CL, et al. Genesis. 2000 Jan;26(1):15-25. Genesis. 2000. PMID: 10660670

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