Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 6

1.

Further genetic analysis of two autosomal dominant mouse eye defects, Ccw and Pax6(coop).

Lyon MF, Bogani D, Boyd Y, Guillot P, Favor J.

Mol Vis. 2000 Oct 31;6:199-203.

2.

PAX6 mutations reviewed.

Prosser J, van Heyningen V.

Hum Mutat. 1998;11(2):93-108. Review.

PMID:
9482572
3.

Congenital hereditary cataracts.

Graw J.

Int J Dev Biol. 2004;48(8-9):1031-44. Review.

4.

Cataract mutations and lens development.

Graw J.

Prog Retin Eye Res. 1999 Mar;18(2):235-67. Review.

PMID:
9932285
5.

Aniridia: recent achievements in paediatric practice.

Ivanov I, Shuper A, Shohat M, Snir M, Weitz R.

Eur J Pediatr. 1995 Oct;154(10):795-800. Review.

PMID:
8529675
6.

[Molecular mechanisms of the pathway formation in the fetal rat cerebral neocortex].

Kawano H, Kawamura K.

Tanpakushitsu Kakusan Koso. 2000 Feb;45(3 Suppl):279-85. Review. Japanese. No abstract available.

PMID:
10707631

Supplemental Content

Support Center