What causes the abnormal phenotype in a 49,XXXXY male? Gloria E. SartoPriscila G. OttoEeva Therman Original Investigations Pages: 1 - 4
Prenatal diagnosis of cystic fibrosis using linked DNA markers and microvillar intestinal enzyme analysis J. Edward SpenceGregory J. BuffoneArthur L. Beaudet Original Investigations Pages: 5 - 10
Hydatidiform mole: genetic origin in polyploid conceptuses Lars O. VejerslevJørgen DissingHanne Poulsen Original Investigations Pages: 11 - 19
Molecular gene mapping of human aldolase A (ALDOA) gene to chromosome 16 A. KukitaM. C. YoshidaK. Hori Original Investigations Pages: 20 - 26
Structure of an abnormal messenger RNA for argininosuccinate synthetase in citrullinemia Keiko KobayashiHitoshi IchikiTadao Yoda Original Investigations Pages: 27 - 32
A null allele of esterase D is a marker for genetic events in retinoblastoma formation Wen-Hwa LeeRobert BooksteinEva Y. -H. P. Lee Original Investigations Pages: 33 - 36
Sequential G- to R-banding for high resolution chromosome analysis Betsy HirschRosalie MackDiane Arthur Original Investigations Pages: 37 - 39
Polymorphic DNA haplotypes at the human phenylalanine hydroxylase locus and their relationship with phenylketonuria Ranaiit ChakrabortyAlan S. LidskySavio L. C. Woo Original Investigations Pages: 40 - 46
Construction of a human ventricular cDNA library and characterization of a beta myosin heavy chain cDNA clone Mark A. JandreskiChoong-Chin Liew Original Investigations Pages: 47 - 53
Two sisters with a distal deletion at the Xq26/Xq27 interface: DNA studies indicate that the gene locus for factor IX is present Charles SchwartzNaomi FitchRoger Stevenson Original Investigations Pages: 54 - 57
The 35 kd pulmonary surfactant-associated protein is encoded on chromosome 10 Gail BrunsHelene StrohJoanna Floros Original Investigations Pages: 58 - 62
Phosphofructokinase activity in fibroblasts aneuploid for chromosome 21 K. Göran AnnerénJulie R. KorenbergCharles J. Epstein Original Investigations Pages: 63 - 65
Human ferritin H and L sequences lie on ten different chromosomes John R. McGillSusau L. NaylorJames W. Drysdale Original Investigations Pages: 66 - 72
Electron microscopy as a means for carrier detection and genetic counselling in families at risk of tuberous sclerosis I. HausserI. Anton-Lamprecht Original Investigations Pages: 73 - 80
Electron microscopic investigations of synaptonemal complexes in an infertile human male carrier of a pericentric inversion inv(1)(p32q42) J. BatanianM. A. Hulten Original Investigations Pages: 81 - 89
A hypervariable region at the D19S11 locus N. E. BurokerL. BuftonM. Litt Original Investigations Pages: 90 - 95
X-linked immunodeficiency with hyperimmunoglobulinemia M appears to be linked to the DXS42 restriction fragment length polymorphism locus E. J. B. M. MensinkA. ThompsonR. K. B. Schuurman Original Investigations Pages: 96 - 99
De novo t(2;13)(p24.3;q14.2) and retinoblastoma Yéronique BlanquetCatherine TurleauJ. de Grouchy Short Communications Pages: 102 - 105
A new translocation t(1;4;11) in congenital acute nonlymphocytic leukemia (acute myeloblastic leukemia) A. SelypesA. László Short Communications Pages: 106 - 108
First trimester abortions associated with a translocation t(1;20)(p36;p11) K. MadanJ. Kleinhout Case Observed Pages: 109 - 109