E-LIB Suche - Ergebnisse für: Lehmann, Ordan J.

1

The Axenfeld–Rieger Syndrome Gene FOXC1 Contributes to Left..:

Chrystal, Paul W ; French, Curtis R ; Jean, Francesca...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7912076/. , 2021

Link: http://www.ncbi.nlm.nih...

2

Genetic background-dependent role of Egr1 for eyelid develo..:

Oh, Jangsuk ; Wang, Yujuan ; Chen, Shida...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5576810/. , 2017

Link: http://www.ncbi.nlm.nih...

3

Changes at CMAJ:

Lehmann, Ordan J
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4818138/. , 2016

Link: http://www.ncbi.nlm.nih...

4

Identification of additional risk loci for stroke and small..:

Chauhan, Ganesh ; Arnold, Corey R ; Chu, Audrey Y...
http://eprints.gla.ac.uk/148442/1/148442.pdf. , 2016

Link: http://eprints.gla.ac.uk..

5

Mutation of FOXC1 and PITX2 induces cerebral small-vessel d..:

French, Curtis R ; Seshadri, Sudha ; Destefano, Anita L...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC. , 2014

Link: http://www.ncbi.nlm.nih...

6

Mutations in PIK3R1 Cause SHORT Syndrome:

Dyment, David A ; Smith, Amanda C ; Alcantara, Diana...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3710754. , 2013

Link: http://www.ncbi.nlm.nih...

7

Forkhead box transcription factor FoxC1 preserves corneal t..:

Seo, Seungwoon ; Singh, Hardeep P ; Lacal, Pedro M...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3277512. , 2012

Link: http://www.ncbi.nlm.nih...

8

Reply to Chakrabarti et al.: Corneal angiogenesis in patien..:

Seo, Seungwoon ; Singh, Hardeep P ; Lacal, Pedro M...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3386086. , 2012

Link: http://www.ncbi.nlm.nih...

9

The role of forkhead genes in eye development and disease:

Lehmann, Ordan Jacob
https://discovery.ucl.ac.uk/id/eprint/10101134/1/The_role_of_forkhead_genes_in_.pdf. , 2003

Link: https://discovery.ucl.ac..

10

The Axenfeld–Rieger Syndrome Gene FOXC1 Contributes to Left..:

Paul W. Chrystal ; Curtis R. French ; Francesca Jean...
Human Genomics and Genetic Diseases. , 2021

Link: https://doi.org/10.3390/..

11

The Axenfeld–Rieger Syndrome Gene FOXC1 Contributes to Left..:

Paul W. Chrystal ; Curtis R. French ; Francesca Jean...
https://www.mdpi.com/2073-4425/12/2/170. , 2021

Link: https://doi.org/10.3390/..

12

Genetics and therapy for pediatric eye diseases:

Holly.Y. Chen ; Ordan J. Lehmann ; Anand Swaroop
http://www.sciencedirect.com/science/article/pii/S2352396421001535. , 2021

Link: https://doi.org/10.1016/..

13

Morphogenetic defects underlie Superior Coloboma, a newly i..:

Jennifer C Hocking ; Jakub K Famulski ; Kevin H Yoon...
http://europepmc.org/articles/PMC5862500?pdf=render. , 2018

Link: https://doi.org/10.1371/..

14

Identification of additional risk loci for stroke and small..:

Agnieszka Slowik ; Aki S. Havulinna ; Albert Vernon Smith...
10779/lincoln.24364672.v1. , 2016

Link: https://figshare.com/art..

15

Identification of additional risk loci for stroke and small..:

Agnieszka Slowik ; Aki S. Havulinna ; Albert Vernon Smith...
http://hdl.handle.net/10779/lincoln.24364672.v1. , 2016

Link: http://hdl.handle.net/10..