25. Galactosemia. Repository identification Nos . GM-52 and 

 GM-53. W.J. Mellman, T.A. Tedesco, A.E. Greene, L.L. 

 Coriell. Cytogenet. Cell Genet. 15:198-199 (1975) 



26. Homozygous familial hypercholesterolemia (receptor-negative 

 type). Repository identification No. GM-361. J.L. Goldstein, 

 M.S. Brown, A.E. Greene, L.L. Coriell. Cytogenet. Cell Genet. 

 15:357-359 (1975) 



27. A double translocation culture t(5;15) t(9;ll) with partial 

 deletion of the short arm of chromosome 5. Repository iden- 

 tification No. GM-344. L. Jackson, M. Barr, M. Aronson, A.E. 

 Greene, L.L. Coriell. Cytogenet. Cell Genet. 15:400-401 

 (1975) 



28. A (6;18) translocation, 46 chromosomes. Repository iden- 

 tification No. GM-610. H.P. Klinger, M.M. Aronson, A.E. 

 Greene, L.L. Coriell. Cytogenet. Cell Genet. 15:402-403 

 (1975) 



29. An (X;3) translocation, balanced, 46 chromosomes. Repository 

 identification No. GM-194. A. de la Chapelle, J. Schroder, 

 H.P. Klinger, M.M. Aronson, R.C. Miller, A.E. Greene, L.L. 

 Coriell. Cytogenet. Cell Genet. 15:404-405 (1975) 



30. A (13;22) translocation, 46 chromosomes. Repository iden- 

 tification No. GM-627. H.J. Kim, K. Hirschhorn, L.Y.F. Hsu, 

 M.M. Aronson, A.E. Greene, L.L. Coriell. Cytogenet. Cell 

 Genet. 15:406-407 (1975) 



157 



