Chromosomes in the Cornelia de Lange syndrome Bente BeckMargareta Mikkelsen Review Articles Pages: 271 - 276
Expression of aromatic polycyclic hydrocarbon-induced monooxygenase (aryl hydrocarbon hydroxylase) in man x mouse hybrids is associated with human chromosome 2 Friedrich J. WiebelPeter HlavicaK. H. Grzeschik Original Investigations Pages: 277 - 280
X-linked mental retardation with the fragile X. A study of 15 families J. F. MatteiM. G. MatteiF. Giraud Original Investigations Pages: 281 - 289
X-autosome translocation with a breakpoint in Xq22 in a fertile woman and her 47,XXX infertile daughter K. MadanP. G. A. HompesC. E. Ford Original Investigations Pages: 290 - 296
Genetic and clinical studies in 13 patients with the Wolf-Hirschhorn syndrome [del(4p)] Miriam G. WilsonJoseph W. TownerPaul Brager Original Investigations Pages: 297 - 307
Paternal or maternal origin of human i(Xq) isochromosomes P. A. OttoPriscila G. Otto Original Investigations Pages: 308 - 309
Partial inversion of the secondary constriction of chromosome 9. Does it exist? M. G. MatteiJ. F. MatteiF. Giraud Original Investigations Pages: 310 - 316
Assignment of adenosine deaminase complexing protein (ADCP) gene(s) to human chromosome 2 in rodent-human somatic cell hybrids Elly Herbschleb-VoogtKarl-Heinz GrzeschikP. Meera Khan Original Investigations Pages: 317 - 323
Mental development of unselected children with sex chromosome abnormalities J. NielsenA. M. SørensenK. Sørensen Original Investigations Pages: 324 - 332
H-Y antigen in Turner's syndrome patients with different sex chromosome constitutions W. EngelB. KlemmeI. Hansmann Original Investigations Pages: 333 - 336
Nondisjunction of a translocation-chromosome t(4;13) M. WestmeierP. KaiserI. Ribhegge Original Investigations Pages: 337 - 341
NORs and statellite associations in a family with 13/14 translocation Jovanka NikolišVladimir KekićVukosava Diklić Original Investigations Pages: 342 - 344
A new meiotic mutation: Desynapsis of individual bivalents C. TempladoF. VidalJ. Egozcue Original Investigations Pages: 345 - 348
Cytogenetic effects of cigarette smoke condensates in vitro and in vivo Stephan MadleAnke KorteGünter Obe Original Investigations Pages: 349 - 352
Prenatal diagnosis of Hurler's syndrome—Biochemical studies on the affected fetus Tomoyasu IkenoRyoji MinamiYuhei Takasago Original Investigations Pages: 353 - 359
Genetic polymorphism of the B subunit of human coagulation factor XIII: Another classification Y. KeraH. NishimukaiK. Yamasawa Original Investigations Pages: 360 - 364
Transferrin (Tf) subtyping on agarose: A new technique for isoelectric focusing Dale DykesHerbert Polesky Original Investigations Pages: 365 - 366
Familial dwarfism with high IR-GH: Report of two affected sibs with genetic and epidemiologic considerations P. H. SaldanhaS. P. A. Toledo Original Investigations Pages: 367 - 372
Characterization of cells of amniotic fluids by immunological identification of intermediate-sized filaments: Presence of cells of different tissue origin M. CremerI. TreissW. W. Franke Original Investigations Pages: 373 - 379
Meiotic arrest at first spermatocyte level: A new inherited infertility disorder J. M. CantúF. RivasB. Ibarra Original Investigations Pages: 380 - 385
Population, formal genetics, and linkage relations of the phosphoglycolate phosphatase (PGP)—E.C.3.1.3.18 Waltraut BrinkM. P. BaurCh. Rittner Original Investigations Pages: 386 - 388
Sister chromatid exchange in newborns Norma H. HatcherErnest B. Hook Original Investigations Pages: 389 - 391
Prenatal diagnosis of genetic disorders of the skin by means of electron microscopy I. Anton-Lamprecht Original Investigations Pages: 392 - 405
In vitro differentiation of diakinesis figures in human testis Diana Curtis Original Investigations Pages: 406 - 411
Population heteromorphisms of Ag-stained nucleolus organizer regions (NORs) in the acrocentric chromosomes of East Indians Ram S. VermaCarole BenjaminHarvey Dosik Original Investigations Pages: 412 - 415
A rapid culture-harvest protocol for amniotic cell cultures Barathur R. RajendraLeonard J. SciorraMing-liang Lee Short Communications Pages: 416 - 418
A method for the sequential study of synaptonemal complexes by light and electron microscopy J. NavarroF. VidalJ. Egozcue Short Communications Pages: 419 - 421
Familial reciprocal translocation t(9;13)(p11;p12) investigated by silver staining and in situ hybridisation Jennifer M. VarleyJohn GosdenMaj Hultén Clinical Case Reports Pages: 422 - 428
Duplication 15q22»15qter and its phenotypic expression M. J. GregoireJ. BoueL. Zergollern Clinical Case Reports Pages: 429 - 433
An unusual pedigree with retinoblastoma. Does it shed light on the delayed mutation and host resistance theories? Sarah BundeyJohn E. N. Morten Clinical Case Reports Pages: 434 - 436
