Meiotic chromosomes in an infertile male with an unbalanced Y/13 translocation Diana J. Curtis Original Investigations Pages: 249 - 254
Pitfalls in the use of chromosome variants for paternity dispute cases Yasuo NakagomeTeruo KitagawaToshiyuki Ando Original Investigations Pages: 255 - 260
The Chicago variant of clinical galactosemia Claramma M. ChackoRebecca S. WappnerHenry L. Nadler Original Investigations Pages: 261 - 270
The human PGM-2 and its chromosomal localization in man-mouse hybrids Lucie M. M. WijnenK. -H. GrzeschikP. Meera Khan Original Investigations Pages: 271 - 278
Regional chromosomal localization of the human gene for galactose-1-phosphate uridyltransferase N. C. SunC. R. Y. SunE. H. Y. Chu Original Investigations Pages: 279 - 284
Nucleolus organizer and N-band distribution in morphologic and fluorescence variants of human chromosomes N. ArchidiaconoA. de CapoaM. Rocchi Original Investigations Pages: 285 - 289
Linkage relationships of Lp and Ag serum lipoproteins with 25 polymorphic markers K. K. NamboodiriR. C. ElstonC. Hames Original Investigations Pages: 291 - 297
Rapid determination of polyploidy in human chrorionic tissue sections K. RiekkiJ. E. BaillieD. L. Baillie Original Investigations Pages: 299 - 302
Population genetics of α1-Antitrypsin in the Netherlands E. C. KlasenC. FrankenL. F. Bernini Original Investigations Pages: 303 - 313
Phosphoglucose isomerase (PGI) variants in the Netherlands S. G. WelchH. A. BartstraR. A. Geerdink Original Investigations Pages: 315 - 317
Genetic markers in Libyan Jews Batsheva Bonné-TamirSarah AshbelJehudit Modai Original Investigations Pages: 319 - 328
A cytogenetic survey of 200 unclassifiable mentally retarded children with congenital anomalies and 200 normal controls Avirachan T. TharapelRobert L. Summitt Original Investigations Pages: 329 - 338
Inversion 19 and isochromosome short arm 17 or 18 Johannes NielsenAkira HommaVagn Holm Clinical Case Reports Pages: 347 - 350
The 48,XXXX/49,XXXXY/49,XXXX,i(Yq) mosaicism in a 3-year-old boy from a twin pregnancy Bogdan KałuzewskiDanuta PodkulLucjusz Jakubowski Clinical Case Reports Pages: 355 - 359
Three cases of hereditary hemolytic anemia with pyrimidine 5′-nucleotidase deficiency in a Japanese family Shiro MiwaKoji NakashimaKoichiro Nomura Clinical Case Reports Pages: 361 - 364