Genotyping of mitochondrial aldehyde dehydrogenase in blood samples using allele-specific oligonucleotides: comparison with phenotyping in hair roots H. Werner GoeddeSurjit SinghYong K. Paik Original Investigations Pages: 305 - 307
Myotonic dystrophy is closely linked to the gene for muscle-type creatine kinase (CKMM) H. G. BrunnerR. G. KornelukH. -H. Ropers Original Investigations Pages: 308 - 310
Detection of 1q polysomy in interphase nuclei of human solid tumors with a biotinylated probe E. Viegas-PéquignotM. JeanpierreB. Dutrillaux Original Investigations Pages: 311 - 314
Gene of X-chromosomal congenital stationary night blindness is closely linked to DXS7 on Xp Andreas GalAlbert SchinzelLiesbeth M. Bleeker-Wagemakers Original Investigations Pages: 315 - 318
A severe autosomal recessive acromesomelic dysplasia, the Hunter-Thompson type, and comparison with the Grebe type Leonard O. Langer Jr.Jaroslav CervenkaMauricio Camargo Original Investigations Pages: 323 - 328
Investigations of chorionic villi after chorionic villus sampling (CVS) J. RüschoffA. KöhlerE. D. Steuber Original Investigations Pages: 329 - 334
Mild hemophilia A resulting from Arg-to-Leu substitution in exon 26 of the factor VIII gene Hiroshi InabaMichio FujimakiStylianos E. Antonarakis Original Investigations Pages: 335 - 338
Localization of human c-mos to chromosome band 8q11 in leukemic cells with the t(8;21) (q22;q22) Christine M. MorrisJacqueline BowenPeter H. Fitzgerald Original Investigations Pages: 339 - 342
Molecular deletion patterns in Duchenne and Becker type muscular dystrophy S. Liechti-GallatiM. KoenigH. Moser Original Investigations Pages: 343 - 348
Rapid isolation of moderate and highly polymorphic DNA fragments mapping close to WT (Wilms' tumour) and AN2 (aniridia) on chromosome 11 Patricia A. BoydSheila ChristieDavid J. Porteous Original Investigations Pages: 349 - 352
Study of a family with a fragile site of the X chromosome at Xq27–28 without mental retardation M. A. VoelckelN. PhilipJ. F. Mattei Original Investigations Pages: 353 - 357
Detection of single-copy genes by nonisotopic in situ hybridization on human chromosomes Dorra CherifOlivier BernardRoland Berger Original Investigations Pages: 358 - 362
Molecular genetic diagnosis of sickle cell disease using dried blood specimens on blotters used for newborn screening David C. JinksMikeanne MinterEdward R. B. McCabe Original Investigations Pages: 363 - 366
Cytogenetic analysis of in vitro fertilization (IVF) failures M. H. E. C. PietersJ. P. M. GeraedtsP. P. C. A. Menheere Original Investigations Pages: 367 - 370
Mutation analysis of β-thalassemia genes in a German family reveals a rare transversion in the first intron A. EigelJ. SchneeJ. Horst Original Investigations Pages: 371 - 372
DNA haplotype analysis at the phenylalanine hydroxylase locus in the Turkish population Uta Lichter-KoneckiMagdalena SchlotterDavid Konecki Original Investigations Pages: 373 - 376
Induction of the fragile X on BrdU-substituted chromosomes with direct visualization of sister chromatid exchanges on banded chromosomes Niels Tommerup Original Investigations Pages: 377 - 381
Confirmation and refinement of the localisation of the c-MEL locus on chromosome 19 by physical and genetic mapping E. NimmoR. -A. PaduaK. J. Johnson Original Investigations Pages: 382 - 384
Regional localization and molecular characterization of a DNA sequence on the long arm of chromosome 22 Elisabeth GöttertReinhold MetzdorfNikolaus Blin Short Communications Pages: 385 - 387
Segregation frequency in microcephaly M. SujathaC. Kusuma KumariJ. S. Murty Short Communications Pages: 388 - 390
A new polymorphic DNA probe pS43 derived from a flow sorted library is assigned to human chromosome 20q13 Susanne SchnittgerFriedrich BeermannIngo Hansmann DNA Variants Pages: 391 - 392
