Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

My NCBI Filters
Text availability
Article attribute
Article type
Publication date

Search Results

3,201 results
Filters applied: . Clear all Results are displayed in a computed author sort order. Results by year timeline is unavailable
Page 1
Inbreeding in recessive diseases.
Tchen P, Bois E, Feingold J, Feingold N, Kaplan J. Tchen P, et al. Among authors: kaplan j. Hum Genet. 1977 Sep 22;38(2):163-7. doi: 10.1007/BF00527398. Hum Genet. 1977. PMID: 302820
Phenotype-genotype correlations in X linked retinitis pigmentosa.
Kaplan J, Pelet A, Martin C, Delrieu O, Aymé S, Bonneau D, Briard ML, Hanauer A, Larget-Piet L, Lefrançois P, et al. Kaplan J, et al. J Med Genet. 1992 Sep;29(9):615-23. doi: 10.1136/jmg.29.9.615. J Med Genet. 1992. PMID: 1357178 Free PMC article.
A gene for Usher syndrome type I (USH1A) maps to chromosome 14q.
Kaplan J, Gerber S, Bonneau D, Rozet JM, Delrieu O, Briard ML, Dollfus H, Ghazi I, Dufier JL, Frézal J, et al. Kaplan J, et al. Genomics. 1992 Dec;14(4):979-87. doi: 10.1016/s0888-7543(05)80120-x. Genomics. 1992. PMID: 1478676
Mapping the eye diseases.
Frézal J, Kaplan J, Dollfus H. Frézal J, et al. Among authors: kaplan j. Ophthalmic Paediatr Genet. 1992 Jun;13(2):37-47. doi: 10.3109/13816819209087603. Ophthalmic Paediatr Genet. 1992. PMID: 1495766 Review.
3,201 results