Nonsyndromic congenital retinal nonattachment gene maps to human chromosome band 10q21GHIASVAND, N. M; KANIS, A. B; HELMS, C et al.American journal of medical genetics. 2000, Vol 90, Num 2, pp 165-168, issn 0148-7299Article

Prenatal ultrasound findings in hydrolethalus : continuing difficulties in diagnosisNORGARD, M; YANKOWITZ, J; RHEAD, W et al.Prenatal diagnosis. 1996, Vol 16, Num 2, pp 173-179, issn 0197-3851Article

The forkhead transcription factor gene FKHL7 is responsible for glaucoma phenotypes which map to 6p25NISHIMURA, D. Y; SWIDERSKI, R. E; ALWARD, W. L. M et al.Nature genetics. 1998, Vol 19, Num 2, pp 140-147, issn 1061-4036Article

Homozygosity mapping of achromatopsia to chromosome 2 using DNA poolingARBOUR, N. C; ZLOTOGORA, J; KNOWLTON, R. G et al.Human molecular genetics (Print). 1997, Vol 6, Num 5, pp 689-694, issn 0964-6906Article

Genomic organization, 5'-flanking region, and chromosomal localization of the human RGS3 geneCHATTERJEE, T. K; EAPEN, A; KANIS, A. B et al.Genomics (San Diego, Calif.). 1997, Vol 45, Num 2, pp 429-433, issn 0888-7543Article