Ring chromosome 10 Associated with multiple congenital malformations G. SimoniF. RossellaC. Piria-Schwarz Original Investigations Pages: 117 - 121
Interstitial deletion of the short arm of chromosome 2 in a moderately mentally retarded boy without gross clinical stigmata J. P. FrynsP. De WaeleH. Van Den Berghe Original Investigations Pages: 123 - 125
Multibranched chromosomes 1, 9, and 16 in a patient with combined IgA and IgE deficiency L. TiepoloPaola MaraschioC. Romano Original Investigations Pages: 127 - 137
Localisation du gène phosphoglycolate phosphatase (PGP) sur le chromosome 16 par l'hybridation cellulaire interspecifique Dominique WeilNguyen Van CongJ. Frézal Original Investigations Pages: 139 - 145
Complete (classic) hydatidiform mole with 46,XY karyotype of paternal origin U. SurtiA. E. SzulmanS. O'Brien Original Investigations Pages: 153 - 155
An r(22)(p11→q13) in a moderately mentally retarded girl V. AllerJ. A. AbrisquetaJ. Del Mazo Original Investigations Pages: 157 - 162
The use of bone core biopsies for cytogenetic analysis Paulette MartinJanet D. RowleyJoseph M. Baron Original Investigations Pages: 163 - 166
Reduced frequency of sister chromatid exchanges in human lymphocytes cultured with autologous serum P. K. GhoshReita Nand Original Investigations Pages: 167 - 170
Structural differences in reciprocal translocations A. Daniel Original Investigations Pages: 171 - 182
Transplacental mutagenesis: The micronucleus test on fetal mouse blood M. -T. KingD. Wild Original Investigations Pages: 183 - 194
Detection of carriers and prenatal diagnosis for fucosidosis in Calabria P. DurandR. GattiG. Romeo Original Investigations Pages: 195 - 201
Genetic load in an isolated tribal population of south India Aloke K. GhoshPartha P. Majumder Original Investigations Pages: 203 - 208
Hb E gene in imphal, manipur (India) M. R. ChakravarttiAmal Kumar Roy Short Communications Pages: 209 - 211
G6PD deficiency with Gd(-)A like variant in a Chinese family from Cambodia J. L. ViallardD. CottreauB. Dastugue Short Communications Pages: 213 - 215
Human pancreatic amylase polymorphism: Formal genetics and population genetics J. KömpfG. SiebertH. Ritter Short Communications Pages: 217 - 220
Serum albumin variants from populations of Andhra Pradesh, S. India P. R. RaoJ. D. GoudB. R. Swamy Short Communications Pages: 221 - 224
6-PGD polymorphism: A fast ‘Elcho’ variant found in Finland Kirsti Virtaranta-KnowlesHarri R. Nevanlinna Short Communications Pages: 225 - 226
Down's syndrome in brother and sister without evident trisomy 21 C. ParloirJ. P. FrynsH. Van den Berghe Clinical Case Reports Pages: 227 - 230
A girl with karyotype 46,XX,del(7)(pter→q32:) Ursula FriedrichOle ØsterballeJan Jørgensen Clinical Case Reports Pages: 231 - 235
Primary mesodermal dysgenesis of the cornea (Peters' anomaly) in two brothers M. BoelJ. TimmermansH. Van den Berghe Clinical Case Reports Pages: 237 - 240