Xeroderma pigmentosum (complementation group D) mutation is present in patients affected by trichothiodystrophy with photosensitivity M. StefaniniP. LagomarsiniF. Nuzzo Original Investigations Pages: 107 - 112
DNA polymorphism related to the idiopathic hemochromatosis gene: evidence in a recombinant family Véronique DavidPascale PaulM. Bourel Original Investigations Pages: 113 - 120
The single copy gene coding for human α1 (IV) procollagen is located at the terminal end of the long arm of chromosome 13 C. D. BoydKaren WelikyEllen Magenis Original Investigations Pages: 121 - 125
A 45,X male with a Yp/18 translocation Emanuela MaseratiF. WaibelU. Wolf Original Investigations Pages: 126 - 132
Assignment of a human beta-crystallin gene to 17cen-q23 R. S. SparkesT. MohandasJ. Horwitz Original Investigations Pages: 133 - 136
Isolation of transcribed DNA sequences from chromosome 21 using mouse fetal cDNA Tohru YokoiM. LovettC. J. Epstein Original Investigations Pages: 137 - 142
Wiedemann-Beckwith syndrome: presentation of clinical and cytogenetic data on 22 new cases and review of the literature M. J. PettenatiJ. L. HainesD. D. Weaver Original Investigations Pages: 143 - 154
Regional localisation of X chromosome short arm probes Karin PaulsenSusan ForrestKay Davies Original Investigations Pages: 155 - 159
Orosomucoid (ORM) typing by isoelectric focusing: evidence for two structural loci ORM1 and ORM2 I. YuasaK. UmetsuM. Robinet-Levy Original Investigations Pages: 160 - 161
The same “TATA” box β-thalassemia mutation in Chinese and US blacks: another example of independent origins of mutation Shangzhi HuangCorinne WongHaig H. Kazazian Jr. Original Investigations Pages: 162 - 164
ApoA-I related DNA polymorphism in humans with coronary heart disease Monika BuraczynskaJanusz HanzlikMarek Grzywa Original Investigations Pages: 165 - 167
Genetic linkage between X-linked retinitis pigmentosa and DNA probe DXS7 {L1.28}: further linkage data, heterogeneity testing, and risk estimation J. F. ClaytonA. F. WrightS. S. Bhattacharya Original Investigations Pages: 168 - 171
Gene localisation of X-linked hypohidrotic ectodermal dysplasia (C-S-T syndrome) K. D. MacDermotR. M. WinterS. Malcolm Original Investigations Pages: 172 - 173
Identity of the polymorphisms for esterase D and S-formylglutathione hydrolase in red blood cells H. EibergJ. Mohr Original Investigations Pages: 174 - 175
Evidence that S-formylglutathione hydrolase and esterase D polymorphisms are identical F. ApeshiotisK. Bender Short Communications Pages: 176 - 177
Integrity of the thyroglobulin locus in tricho-rhino-phalangeal syndrome II Huguette BrocasErica M. BühlerG. Vassart Short Communications Pages: 178 - 180
Estimation of the male to female ratio of mutation rates from the segregation of X-chromosomal DNA haplotypes in Duchenne muscular dystrophy families C. R. MüllerT. Grimm Short Communications Pages: 181 - 183
Dominant autosomal muscular dystrophy with early contractures and cardiomyopathy (Hauptmann-Thannhauser) P. E. Becker Short Communications Pages: 184 - 184
Hypomelanosis of Ito (incontinentia pigmenti achromians) and mosaicism for a microdeletion of 15q1 Catherine TurleauF. TaillardJ. de Grouchy Clinical Case Reports Pages: 185 - 187
8q24.12 Interstitial deletion in trichorhinophalangeal syndrome type I J. P. FrynsH. Van den Berghe Clinical Case Reports Pages: 188 - 189
Deletion 14q(q24.3 to q32.1) syndrome: significance of peculiar facial appearance in its diagnosis, and deletion mapping of (α1-antitrypsin) Y. YamamotoR. SawaS. Ikemoto Clinical Case Reports Pages: 190 - 192
De novo DNA microdeletion in a girl with Turner syndrome and Duchenne muscular dystrophy J. ChellyF. MarlhensJ. -C. Kaplan Clinical Case Reports Pages: 193 - 196
Paracentric inversions in human chromosome 7 M. SchmidT. HaafM. Zorn Clinical Case Reports Pages: 197 - 199
Autosomal dominant macroglossia in two unrelated families M. C. ReynosoA. HernándezJ. M. Cantú Clinical Case Reports Pages: 200 - 202
Yqs Resulting from a reciprocal Y;15 translocation in the father of a 46,X,i(Xq) girl A. M. JosephM. JagannathI. M. Thomas Cases Observed Pages: 203 - 203
Polymorphism of 6-PGD in South Korea: a new genetic variant 6-PGD Korea Heide-G. BenkmannY. K. PaikH. W. Goedde Genetic Variant Register Pages: 204 - 205
Di George syndrome and 22q11 rearrangements S. AugusseauS. JoukM. Prieur Letters to the Editors Pages: 206 - 206
Rare, polymorphic, and common fragile sites: a classification F. Hecht Letters to the Editors Pages: 207 - 208
