X-linked dominant inherited diseases with lethality in hemizygous males Roswitha Wettke-SchäferGisela Kantner Review Articles Pages: 1 - 23
The distribution of chromosomal genotypes associated with Turner's syndrome: livebirth prevalence rates and evidence for diminished fetal mortality and severity in genotypes associated with structural X abnormalities or mosaicism E. B. HookDorothy Warburton Original Investigations Pages: 24 - 27
Cytologic and molecular analysis of 46,XXq- cells to identify a DNA segment that might serve as a probe for a putative human X chromosome inactivation center U. TantravahiD. A. KirschnerS. Latt Original Investigations Pages: 33 - 38
Frequency of fragile X chromosomes, fra(X), in lymphocytes in relation to blood storage time and culture techniques Christa FonatschE. Schwinger Original Investigations Pages: 39 - 41
Cytogenetic effects of chemotherapy with three combinations of anti-tubercular drugs involving isoniazid, thiacetazone, para-aminosalicylic acid and streptomycin on human lymphocytes: chromosome aberrations, sister chromatid exchanges and mitotic index Madhuri JajuManjula JajuY. R. Ahuja Original Investigations Pages: 42 - 49
Morquio-B disease, spondyloepiphyseal dysplasia associated with acid β-galactosidase deficiency. Report of three cases in one family J. J. van GemundM. A. H. GiesbertsW. J. Kleijer Original Investigations Pages: 50 - 54
Complementation studies between Fanconi's anemia cells with different DNA repair characteristics Sabine ZakrzewskiM. KochK. Sperling Original Investigations Pages: 55 - 57
Investigation of PGM13, PGM16, and PGM17 variants by isoelectric focussing. Evidence for new subtypes of the PGM 1 3 and PGM 1 7 alleles M. I. KambohR. L. Kirk Original Investigations Pages: 58 - 60
The metallothionein-I gene maps to mouse chromosome 8: implications for human Menkes' disease D. R. CoxR. D. Palmiter Original Investigations Pages: 61 - 64
Gene mapping of the gibbon. Its position in primate evolution Catherine TurleauNicole Créau-GoldbergJ. de Grouchy Original Investigations Pages: 65 - 72
Chromosome aberrations induced in patients treated with chemotherapeutic drugs and irradiation for acute lymphatic leukemia K. H. RausherM. Bauchinger Original Investigations Pages: 73 - 79
Variability in the phenotypic expression of abnormal sarcosine metabolism in a family Ellen S. KangJ. SeyerC. Herrera Original Investigations Pages: 80 - 85
46,XX/46,XY chimerism in a phenotypically normal man E. SchoenleW. SchmidE. R. Froesch Clinical Case Reports Pages: 86 - 89
Two cases of the Langer-Giedion syndrome with the same interstitial deletion of the long arm of chromosome 8: 46,XY or XX,del(8)(q23.3q24.13) Y. FukushimaY. KurokiT. Izawa Clinical Case Reports Pages: 90 - 93
Consanguinity in a Turkish family with thrombocytopenia with absent radii (TAR) syndrome M. TeufelH. EndersR. Dopfer Clinical Case Reports Pages: 94 - 96
Interstitial deletion of the long arm of chromosome 3 in a patient with mental retardation and congenital anomalies P. FranceschiniM. Cirillo SilengoM. Biagioli Cases Observed Pages: 97 - 97
Interstitial deletion of the long arm of chromosome 2 (q31q33) in a girl with multiple anomalies and mental retardation P. FranceschiniM. Cirillo SilengoM. Biagioli Cases Observed Pages: 98 - 98
Unusual pericentric inversion inv(9)(p13q11) in a phenotypically normal family M. J. MartínJ. A. Abrisqueta Cases Observed Pages: 100 - 100
