Construction of a chromosome 16-enriched phage library and characterization of several DNA segments from 16p Peter HarrisMarc LalandeSamuel A. Latt Original Investigations Pages: 95 - 103
Familial retinoblastoma (mother and son) with 13q14 deletion Yoshimitsu FukushimaYoshikazu KurokiItsuro Nishigaki Original Investigations Pages: 104 - 107
Variation in the frequency and type of sperm chromosomal abnormalities among normal men Renee H. MartinAlfred W. RademakerJudy Yamamoto Original Investigations Pages: 108 - 114
Mapping of a restriction fragment length polymorphism within the human aldolase B gene Giovanni PaolellaRita SantamariaFrancesco Salvatore Original Investigations Pages: 115 - 117
The fragile site (17)(p12): induction by AT-specific DNA-ligands and population cytogenetics M. SchmidW. FeichtingerE. Weller Original Investigations Pages: 118 - 121
Isolation of a polymorphic genomic clone from chromosome 7 Kevin A. DaviesLaszlo LorandRobert Williamson Original Investigations Pages: 122 - 126
Two different forms of beta myosin heavy chain are expressed in human striated muscle Mark A. JandreskiMichael J. SoleChoong-Chin Liew Original Investigations Pages: 127 - 131
One haplotype is associated with the Swiss type of hereditary persistence of fetal hemoglobin in the Yugoslavian population G. D. EfremovI. GjorgovskiT. H. J. Huisman Original Investigations Pages: 132 - 136
A cytogenetic study directly from chorionic villi of 140 spontaneous abortions Bernd EibenSabine BorgmannIngo Hansmann Original Investigations Pages: 137 - 141
Localization of the human multiple drug resistance gene, MDR1, to 7q21.1 D. F. CallenE. BakerI. B. Roninson Original Investigations Pages: 142 - 144
A Y/5 translocation in a 45,X male with cri du chat syndrome Bernhard WeberWerner SchemppAndreas Gal Original Investigations Pages: 145 - 150
Detection of novel centromeric polymorphisms associated with alpha satellite DNA from human chromosome 11 John S. WayeGillian M. GreigHuntington F. Willard Original Investigations Pages: 151 - 156
A comparative mapping study of fragile sites in the human and murine genomes M. DjalaliSabine AdolphH. Hameister Original Investigations Pages: 157 - 162
Confined chorionic mosaicism in prenatal diagnosis Dagmar K. KalousekFred J. DillR. Douglas Wilson Original Investigations Pages: 163 - 167
Hyperphenylalaninemia due to deficiency of 6-pyruvoyl tetrahydropterin synthase C. R. ScriverC. L. ClowA. Niederwieser Original Investigations Pages: 168 - 171
Close linkage of random DNA fragments from Xq 21.3–22 to X-linked agammaglobulinaemia (XLA) S. MalcolmG. de Saint BasileR. J. Levinsky Original Investigations Pages: 172 - 174
A hypervariable repeated sequence on human chromosome 1p36 N. BurokerR. BestwickM. Litt Original Investigations Pages: 175 - 181
Molecular cloning of a pair of human pepsinogen A genes which differ by a Glu→Lys mutation in the activation peptide Marie Pauline J. EversBauke ZelleRune R. Frants Original Investigations Pages: 182 - 187
Follow-up 20 years later of 34 Klinefelter males with karyotype 47,XXY and 16 hypogonadal males with karyotype 46,XY J. NielsenB. Pelsen Original Investigations Pages: 188 - 192
Premature centromere division (PCD): a dominantly inherited cytogenetic anomaly K. MadanD. LindhoutA. Palan Original Investigations Pages: 193 - 196
Crossovers in two German cystic fibrosis families determine probe order for MET, 7C22 and XV-2c/CS.7 W. BergerJ. HeinC. Coutelle Short Communications Pages: 197 - 199
Lack of genetic polymorphism in human skeletal muscle enzymes of the tricarboxylic acid cycle Martine MarcotteMonique ChagnonClaude Bouchard Short Communications Pages: 200 - 200
Gd(+)Cuiabá, a new rare glucose-6-phosphate dehydrogenase variant presenting normal activity Orlando C. O. de BarrettoKimiyo Nonoyama Short Communications Pages: 201 - 202
Split hand, obstructive urinary anomalies and spina bifida or diaphragmatic defect syndrome with autosomal dominant inheritance A. CzeizelA. Losonci Clinical Case Report Pages: 203 - 204