Partial 11q trisomy syndrome Helena PihkoEeva ThermanIrene A. Uchida Review Articles Pages: 129 - 134
Human inherited marker chromosome 22 short-arm enlargement: Investigation of rDNA gene multiplicity, Ag-band size, and acrocentric association Renée BernsteinBronwen DawsonJoan Griffiths Original Investigations Pages: 135 - 139
Regional assignment of arylsulfatase A, mitochondrial aconitase and NADH-cytochrome b5 reductase by somatic cell hybridization M. C. Hors-CaylaC. JunienJ. Frézal Original Investigations Pages: 140 - 143
Translocations involving chromosome 12 Judith H. FordRuth H. RofeRuth P. Pavy Original Investigations Pages: 144 - 148
Fanconi's anemia: Anomaly of enzyme passage through the nuclear membrane? E. WunderU. BurghardtL. Hamilton Original Investigations Pages: 149 - 155
An improved method for Y-body identification and confirmation of a high incidence of YY sperm nuclei M. KlasenM. Schmid Original Investigations Pages: 156 - 161
Characterization of a complex philadelphia translocation (1p-;9q+;22q-) by gene mapping A. H. M. Geurts van KesselA. J. van AgthovenA. Hagemeijer Original Investigations Pages: 162 - 165
A Burkitt-lymphoma variant translocation (2p-; 8q+) in a patient with ALL, L3 (Burkitt type) Janet D. RowleyDania VariakojisMichael Cimino Original Investigations Pages: 166 - 167
Lymphocyte chromosome survey in 42 patients with retinoblastoma: Effort to detect 13q14 deletion mosaicism Tomiko Motegi Original Investigations Pages: 168 - 173
Isoelectric focusing of Gc (vitamin D binding globulin) in parentage testing Dale DykesHerbert PoleskyEdmundo Cox Original Investigations Pages: 174 - 175
Sexual development of patients with isochromosomes for the long arm of the X chromosome Shirley HodgsonDaniel ChiuPaul Polani Original Investigations Pages: 176 - 178
Biochemical, genetic, psychometric, and neuropsychological studies in heterozygotes of a family with globoid cell leucodystrophy (Krabbe's disease) H. ChristomanouS. JafféK. Betke Original Investigations Pages: 179 - 183
Cytogenetic studies in a selected group of mentally retarded children M. MogheZ. M. PatelL. M. Ambani Original Investigations Pages: 184 - 187
Cell culture studies on neurofibromatosis (von Recklinghausen) Winfrid KroneSybille ZörleinRichard Mao Original Investigations Pages: 188 - 193
Hereditary porphobilinogen synthase deficiency in human associated with acute hepatic porphyria Andrea BrandtManfred Doss Original Investigations Pages: 194 - 197
Investigations into sister chromatid exchange in patients under cytostatic therapy Dagrun Düker Original Investigations Pages: 198 - 203
New form of adrenoleukodystrophy Paul J. BenkePatricio F. ReyesJoseph C. Parker Jr. Original Investigations Pages: 204 - 208
Properdin factor B polymorphism in continental Italy and Sardinia Fabio MalavasiEleonora OlivettiAngelo O. Carbonara Original Investigations Pages: 209 - 212
Genetic polymorphism of the complement C2 in Japanese K. TokunagaC. ArakiK. Omoto Original Investigations Pages: 213 - 216
A metastatic malignant melanoma with 24 chromosomes N. B. atkinM. C. Baker Short Communications Pages: 217 - 219
Segregation of a complex rearrangement of chromosomes 6, 7, 8, and 12 through three generations Barbara MeerG. WolffElke Back Clinical Case Reports Pages: 221 - 225
Pericentric inversion of chromosome 1 in three sterile brothers Alejandro GiraldoElizabeth SilvaJesús Guzmán Clinical Case Reports Pages: 226 - 227
The deafness, onycho-osteo-dystrophy, mental retardation syndrome O. SánchezJ. J. M. MazasI. Ortíz de DeMatos Clinical Case Reports Pages: 228 - 230
Langer-Giedion syndrome and deletion of the long arm of chromosome 8 J. P. FrynsN. LoggheH. Van den Berghe Letter to the Editors Pages: 231 - 232
