X long-arm deletions. A review of non-mosaic cases studied with banding techniques Lillian SkibstedH. WesthE. Niebuhr Review Articles Pages: 1 - 5
Localisation of the Becker muscular dystrophy gene on the short arm of the X chromosome by linkage to cloned DNA sequences H. M. KingstonM. SarfaraziP. S. Harper Original Investigations Pages: 6 - 17
Partial deficiency of hypoxanthine-guanine phosphoribosyltransferase with reduced affinity for PP-ribose-P in four related males with gout F. F. SnyderA. E. ChudleyJ. K. Lowe Original Investigations Pages: 18 - 22
Exclusion of chromosomal mosaicism in prenatal diagnosis Uwe ClaussenHelmut SchäferHans J. Trampisch Original Investigations Pages: 23 - 28
Osteogenesis imperfecta: a heterogeneous morphologic phenotype in cultured dermal fibroblasts Andrew P. BorightGerald A. LancasterCharles R. Scriver Original Investigations Pages: 29 - 33
Genetic mapping of the structural gene for antithrombin III to human chromosome 1 F. T. KaoH. G. MorseS. L. C. Woo Original Investigations Pages: 34 - 36
DNA replication and inactivation patterns in structural abnormality of sex chromosomes Mauricio CamargoJaroslav Cervenka Original Investigations Pages: 37 - 47
Polymorphisms of human albumin gene after DNA restriction by Hae III endonuclease S. Lavareda de SouzaM. FrainG. Lucotte Original Investigations Pages: 48 - 51
Heterozygous carriers for Bloom syndrome exhibit a spontaneously increased micronucleus formation in cultured fibroblasts Brigitte FrorathUte Schmidt-PreussHugo W. Rüdiger Original Investigations Pages: 52 - 55
Statistical evaluation of sister chromatid exchanges P. VercauterenE. MeulepasH. Van Den Berghe Original Investigations Pages: 56 - 61
Inherited XX sex reversal in the cocker spaniel dog J. R. SeldenP. S. MoorheadD. F. Patterson Original Investigations Pages: 62 - 69
A new α2HS-glycoprotein typing by isoelectric focusing K. UmetsuS. KashimuraT. Suzuki Original Investigations Pages: 70 - 71
Satellited Y chromosomes: Structure, origin, and clinical significance M. SchmidT. HaafH. Heilbronner Original Investigations Pages: 72 - 85
The phenotype in partial 13q trisomies, apropos of a familial (13;15)(q22;q26) translocation F. RivasH. RiveraJ. M. Cantú Original Investigations Pages: 86 - 93
Persistence of chromosome rearrangements in peripheral lymphocytes from patients treated with melphalan for ovarian carcinoma Bo LambertKerstin HolmbergNina Einhorn Original Investigations Pages: 94 - 98
Fragile (X) expression: Relationship to the cell cycle E. S. CantúPatricia A. Jacobs Original Investigations Pages: 99 - 102
Prevalence of primary adult lactose malabsorption in three populations of northern China Wang YongfaYan YongshanG. Flatz Original Investigations Pages: 103 - 106
No marker (X) syndrome in autistic children Philippus A. VenterJohann Op't HofAndries E. Retief Short Communications Pages: 107 - 107
Y-Dependent polypeptides identified by two-dimensional gel electrophoresis of monozygotic X0 and XY fibroblasts Ulrich MüllerNicole MaierMarco Fraccaro Short Communications Pages: 108 - 110
A list of cloned human DNA sequences-Supplement J. SchmidtkeD. N. Cooper Short Communications Pages: 111 - 114
Expression of an X-linked muscular dystrophy in a female due to translocation involving Xp21 and non-random inactivation of the normal X chromosome Ch. Verellen-DumoulinM. FreundR. G. Worton Clinical Case Reports Pages: 115 - 119
Ring chromosome 21 in a healthy woman with three spontaneous abortions K. Rhomberg Cases Observed Pages: 120 - 120