Reciprocal translocation t(5;6)(p13;q27) through three generations: Case report of cri du chat syndrome T. HashimotoR. TsukinoJ. Furuyama Original Investigations Pages: 145 - 147
Densitometric and visual measurements of human chromosome 21 C. W. YuH. M. DowneyJ. H. Priest Original Investigations Pages: 149 - 153
Hybridization studies of fibroblasts from Hurler, Scheie, and Hurler/Scheie compound patients: Support for the hypothesis of allelic mutants J. J. H. FortuinW. J. Kleijer Original Investigations Pages: 155 - 159
Incidence of chromosomal rearrangements in couples with reproductive loss Nataline B. KardonJessica G. DavisAfina Broekman Original Investigations Pages: 161 - 164
Trisomy 16q21»qter Angiolina GarauG. CrisponiOrsetta Zuffardi Original Investigations Pages: 165 - 167
Trisomy 20pter»q11 in a malformed boy from a t(13;20)(p11;q11) translocation-carrier mother A. Schinzel Original Investigations Pages: 169 - 172
Tertiary trisomy (22q11q),47,+der(22),t(11;22) B. M. BiedermanC. C. LinR. Somerville Original Investigations Pages: 173 - 177
Balanced translocation (10;13) in a father, ascertained through the study of meiosis in semen, and partial trisomy 10q in his son R. MiróC. TempladoJ. Egozcue Original Investigations Pages: 179 - 182
Structural abnormalities of the Y chromosome and abnormal external genitals Satoshi Yanagisawa Original Investigations Pages: 183 - 188
Assignment of a structural gene for a fourth human diaphorase (DIA4) to chromosome 16 in man-mouse somatic cell hybrids K. -H. Grzeschik Original Investigations Pages: 189 - 193
Duplication-deficiency of chromosome 18, resulting from recombination of a paternal pericentric inversion, with a note for genetic counselling J. R. TeyssierF. Bajolle Original Investigations Pages: 195 - 200
Temporary increase in chromosome breakage in an infant prenatally exposed to lead Q. H. QaziCecily MadaharA. M. Yuceoglu Original Investigations Pages: 201 - 203
Banded karyotypes from bone marrow: A clinical useful approach J. C. HozierLeanna L. Lindquist Original Investigations Pages: 205 - 209
Mechanisms of Giemsa banding H. E. WyandtRuth S. AndersonF. Hecht Original Investigations Pages: 211 - 215
Prenatal exclusion of congenital erythropoietic porphyria (Günther's disease) in a fetus at risk J. Ch. DeybachB. GrandchampP. de Berranger Original Investigations Pages: 217 - 221
Atypical segregation of esterase D: Evidence of a rare “silent” allele EsD 0 P. KoziołJanina Stepień Original Investigations Pages: 223 - 225
Glucose-6-phosphate dehydrogenase in Thailand Vicharn Panich Original Investigations Pages: 227 - 228
Is there a PGM1 4 allele specific to Amerindian populations? P. TchenJeanine SégerJ. V. Neel Original Investigations Pages: 229 - 231
α1-antitrypsin (Pi) phenotypes in a village population from the Gambia, West Africa S. G. WelchI. A. McGregorK. Williams Original Investigations Pages: 233 - 235
Satellite associations and silver staining in a case of multiple G and D variants R. Di LerniaM. L. RivaE. Ginelli Original Investigations Pages: 237 - 240
The genetic defect in the various types of human β-galactosidase deficiency H. L. HoeksemaJ. De WitA. Westerveld Original Investigations Pages: 241 - 247
Altered sensitivity to colchicine and PHA in human cultured cells Y. ChamlaMonique RoumyJ. Battin Original Investigations Pages: 249 - 253
Nomarski-optical studies of human chromosomes R-banded with barium hydroxide J. M. J. C. ScheresT. W. J. HustinxG. F. M. Merkx Original Investigations Pages: 255 - 259
Determinants of blood pressure in Japanese-American families N. E. MortonC. L. GulbrandsenA. Kagan Original Investigations Pages: 261 - 266
Expression in fibroblast culture of the satellited-X chromosome associated with familial sex-linked mental retardation P. B. JackyF. J. Dill Short Communications Pages: 267 - 269
The presence of androgen-binding receptors in genital and nongenital skin fibroblasts J. HerfertT. F. WienkerH. H. Ropers Short Communications Pages: 271 - 273
Partial short arm deletion of the X chromosome 46,X,del(X)(qter→p21:) Mary KäosaarA. -V. Mikelsaar Clinical Case Report Pages: 275 - 277
The tetraphocomelia-cleft palate syndrome in identical twins H. FrynsP. GoddeerisH. van den Berghe Clinical Case Report Pages: 279 - 281
Reply to the letter of Prieto et al. Concerning our paper on a case of 13q;18q translocation Y. NakagomeY. Suzuki Letters to the Editors Pages: 283 - 283
A comment on the paper: Recurrence of down syndrome associated with microchromosome by C. Ramos, L. Rivera, J. Benitez, E. Tejedor, and A. Sanchez-Cascos Anna CalabroM. Serena LungarottiB. Dallapiccola Letters to the Editors Pages: 287 - 288