The mucopolysaccharidoses: Inborn errors of glycosaminoglycan catabolism M. CantzJ. Gehler Review Articles Pages: 233 - 255
Formal genetics of Fanconi's anemia T. M. SchroederD. TilgenF. Vogel Original Investigations Pages: 257 - 288
Mental retardation and congenital malformations associated with a ring chromosome 9 S. NakajimaM. YanagisawaY. Nakagome Original Investigations Pages: 289 - 293
Fusion of two apparently intact human X chromosomes Anil K. SinhaSen PathakJames J. Nora Original Investigations Pages: 295 - 300
Localization of the human GLO gene locus B. OlaisenT. Gedde-Dahl Jr.E. Thorsby Original Investigations Pages: 301 - 304
Significance of a new type of human fetal hemoglobin carrying a replacement isoleucine → threonine at position 75 (E 19) of the γ chain G. RiccoU. MazzaL. F. Bernini Original Investigations Pages: 305 - 313
Isolation of mammalian cell mutants deficient in glucose 6-phosphate dehydrogenase by means of a replica-plating technique Dieter WildBernard Hellkuhl Original Investigations Pages: 315 - 322
Fabry's disease: Heterozygote detection by hair root analysis T. GrimmT. F. WienkerH. -H. Ropers Original Investigations Pages: 329 - 334
Evidence for an association between AB0 blood group and goitre G. A. HarrisonA. J. BoyceW. J. Craig Original Investigations Pages: 335 - 337
C and Q bands in long arm of Y chromosomes; are they identical? D. SoudekParvaneh Laraya Short Communications Pages: 339 - 341
A family with a high risk of segregation for an autosomal unbalanced reciprocal translocation Johannes NielsenKirsten RasmussenLissi Bank Lassen Short Communications Pages: 343 - 348
Prenatal diagnosis of congenital anomalies in an intrauterine growth retarded fetus Mitchell S. GolbusBryan D. HallRobert K. Creasy Clinical Case Reports Pages: 349 - 352