Descriptive neuropathology of chromosomal disorders in man F. GullottaHelga RehderA. Gropp Review Articles Pages: 337 - 344
Preferential maternal derivation in inv dup(15) Paola MaraschioOrsetta ZuffardiG. Zamboni Original Investigations Pages: 345 - 350
The ESD polymorphism: Further studies of the ESD2 and ESD5 allele products B. OlaisenA. SivertsT. Gedde-Dahl Original Investigations Pages: 351 - 353
Activity of steroid sulfatase in fibroblasts with numerical and structural X chromosome aberrations H. H. RopersB. MiglA. Westerveld Original Investigations Pages: 354 - 356
Prenatal detection of an accessory chromosome identified as an inversion duplication (15) Gail StettenBernadette Sroka-ZaczekVirginia L. Corson Original Investigations Pages: 357 - 359
Morquio syndrome: Clinical findings in 11 patients with MPS IVA and 2 patients with MPS IVB W. HolzgreveH. GröbeJ. F. Mattei Original Investigations Pages: 360 - 365
H-Y antigen expression in a case of mixed gonadal dysgenesis C. A. Moreira-FilhoA. T. AmaralB. R. Elejalde Original Investigations Pages: 366 - 370
Genetic regulation of γ gene expression: Study of the interaction of β-thalassemia with heterocellular HPFH A. M. SoummerU. TestaJ. Rosa Original Investigations Pages: 371 - 375
Finger ridge-count variation in 45,X Turner's syndrome R. L. JantzG. C. RanyardD. W. Owsley Original Investigations Pages: 376 - 379
The pattern of radiation-induced transmissible aberrations in a human cell culture C. L. Y. LeeO. P. Kamra Original Investigations Pages: 380 - 384
The various phenotypes in Xp deletion. Observations in eleven patients J. P. FrynsP. PetitH. Van den Berghe Original Investigations Pages: 385 - 387
The chromosomal distribution of repetitive DNA sequences within the human β globin gene cluster S. MalcolmP. BartonM. A. Ferguson-Smith Original Investigations Pages: 388 - 393
Genetic variation of hexosaminidase A and arylsulfatase A activity. Correlation study in amnio-maternal paris of cultured cells K. HarzerK. Hayashi Original Investigations Pages: 394 - 398
Serum concentrations of vitamin D-binding protein (Group-specific component) in cystic fibrosis Dorian CoppenhaverFriedrich KueppersBarbara H. Bowman Original Investigations Pages: 399 - 403
Characterization of the biochemical basis of a complete deficiency of the adenine phosphoribosyl transferase (APRT) W. DopplerMonica Hirsch-KauffmannM. Schweiger Original Investigations Pages: 404 - 410
Segregation analysis in hereditary retinoblastoma Catherine Bonaïti-PelliéMarie Louise Briard-Guillemot Original Investigations Pages: 411 - 419
The genetic structure of the kuwaiti population II: The distribution of Q-band chromosomal heteromorphisms Khaled E. Al-NassarCatherine G. PalmerPau-Lo Yu Original Investigations Pages: 423 - 427
Christ-Siemens-Touraine syndrome. Investigations on two large brazilian kindreds with a new estimate of the manifestation rate among carriers M. PinheiroM. T. IderihaS. L. Primo-Parmo Original Investigations Pages: 428 - 431
A simple method for improving the reproductibility of the R-banding technique Alain BernheimRoland Berger Short Communications Pages: 432 - 433
Ultrathin-layer isoelectrofocusing for rapid diagnosis of protein variants H. W. GoeddeH. -G. BenkmannL. Hirth Short Communications Pages: 434 - 436
Sweat pore counts in ectodermal dysplasias J. KleinebrechtK. -H. DegenhardtJ. Svejcar Short Communications Pages: 437 - 439
Prenatal monitoring for wolman's disease in a pregnancy at risk Helene ChristomanouClaudia Čáp Clinical Case Reports Pages: 440 - 441
Meiotic findings in human reciprocal 1;3 translocation Miroslava D. MiéiéSava R. Miéié Clinical Case Reports Pages: 442 - 443
Autosomal recessive “uncomplicated” profound childhood deafness in an arabic family with high consanguinity A. KabarityS. A. Al-AwadiG. Mallalah Clinical Case Reports Pages: 444 - 446
