Human Genetics

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Volume 65, Issue 2

December 1983

35 articles in this issue

Increased satellite association induced by 5′ Bromodeoxyuridine treatment of Phytohemaglutinin-stimulated blood lymphocytes
Jana Musilová
Kyra Michalová
Helena Hoffmanová
Original Investigations Pages: 91 - 93
Cystic fibrosis in the Ohio Amish: Gene frequency and founder effect
Katherine Wood Klinger
Original Investigations Pages: 94 - 98
Effect of oxygen tension on chromosomal aberrations in Fanconi anaemia
H. Joenje
B. Oostra
Original Investigations Pages: 99 - 101
A deficiency mutant of the Gc system
B. Vavrusa
H. Cleve
J. Constans
Original Investigations Pages: 102 - 107
Interferon induction of (2′–5′) oligoisoadenylate synthetase in diploid and trisomy 21 human fibroblasts: Relation to dosage of the interferon receptor gene (IRFC)
J. Weil
Georgianne Tucker
C. J. Epstein
Original Investigations Pages: 108 - 111
Complementation analysis in Gaucher disease using single cell microassay techniques. Evidence for a single “Gaucher gene”
R. A. Gravel
A. Leung
Original Investigations Pages: 112 - 116
A dominantly inherited cytogenetic anomaly: A possible cell division mutant
Noreen L. Rudd
Iluko E. Teshima
Rosanna Weksberg
Original Investigations Pages: 117 - 121
Familial, EsD-linked, retinoblastoma with reduced penetrance and variable expressivity
M. J. Connolly
R. H. Payne
R. D. Lawton
Original Investigations Pages: 122 - 124
Are bowing of long tubular bones and preaxial polydactyly signs of the Meckel syndrome?
F. Majewski
H. Stöß
H. Kemperdick
Original Investigations Pages: 125 - 133
Interstitial deletion for a region in the long arm of chromosome 16
C. C. Lin
R. B. Lowry
F. F. Snyder
Original Investigations Pages: 134 - 138
The sequence of DNA replication in an iso-dicentric X-chromosome in peripheral blood lymphocytes and skin fibroblasts from the same individual
M. S. Lin
M. G. Wilson
Original Investigations Pages: 139 - 143
Methyl green is a substitute for distamycin A in the formation of distamycin A/DAPI C-bands
T. A. Donlon
R. E. Magenis
Original Investigations Pages: 144 - 146
Glutamate pyruvate transaminase null allele in seven new families
Maryellen C. Sparkes
M. Crist
R. S. Sparkes
Original Investigations Pages: 147 - 148
Juvenile idiopathic haemochromatosis: A life-threatening disorder presenting as hypogonadotropic hypogonadism
M. Cazzola
E. Ascari
E. E. Werner
Original Investigations Pages: 149 - 154
The genetic significance of accessory bisatellited marker chromosomes
P. Steinbach
M. Djalali
M. Wolf
Original Investigations Pages: 155 - 164
Mating between two balanced translocation carriers in two unrelated families
B. Dallapiccola
L. Chessa
E. Gandini
Original Investigations Pages: 165 - 168
Genetic linkage relationships between the Xg blood group system and two X chromosome DNA polymorphisms in families with Duchenne and Becker muscular dystrophy
M. Sarfarazi
P. S. Harper
R. Sanger
Original Investigations Pages: 169 - 171
Prenatal diagnosis of Tay-Sachs disease. Reflectometry of hexosaminidase A, B, and C/S bands on zymograms
B. Kustermann-Kuhn
K. Harzer
Original Investigations Pages: 172 - 175
The polymorphism of the vitamin D-binding protein (Gc); Isoelectric focusing in 3 M urea as additional method for identification of genetic variants
J. Constans
H. Cleve
W. Weber
Original Investigations Pages: 176 - 180
A genetic component of the variance of N-acetoxy-2-acetylaminofluorene-induced DNA damage in mononuclear leukocytes determined by a twin study
R. W. Pero
C. Bryngelsson
Å. Nordén
Original Investigations Pages: 181 - 184
Meiotic studies in a series of 1100 infertile and sterile males
J. Egozcue
C. Templado
S. Marina
Original Investigations Pages: 185 - 188
On the identity of arylsulphatase C and steroid sulphatase
G. Burns
Original Investigations Pages: 189 - 189
Protein A radio-assay of H-Y antigen on human leukocytes using mouse and rat antisera and monoclonal antibodies
H. Savikuki
L. C. Andersson
A. de la Chapelle
Original Investigations Pages: 190 - 194
Chromosomal localization of a human myosin heavy-chain gene by in situ hybridization
Gudrun A. Rappold
H.-P. Vosberg
Original Investigations Pages: 195 - 197
Characterization of a human genomic DNA fragment coding for a myosin heavy chain
H. Appelhans
H.-P. Vosberg
Original Investigations Pages: 198 - 203
Four new haplotypes observed in Algerian β-thalassemia patients
C. Beldjord
Claudine Lapouméroulie
D. Labie
Original Investigations Pages: 204 - 206
Regional localization of the human factor IX gene by molecular hybridization
P. F. Chance
Karen A. Dyer
S. M. Gartler
Short Communications Pages: 207 - 208
Sex vesicle loss: A possible explanation of the excess of XO over XXY conceptuses in mice and men
T. Ashley
Short Communications Pages: 209 - 210
Fragile chromosome 16(q22) cause a balanced translocation at the same point
J. M. García-Sagredo
C. San Román
G. Lledo
Clinical Case Reports Pages: 211 - 213
G6PD Sendagi: A new glucose-6-phosphate dehydrogenase variant associated with congenital hemolytic anemia
T. Morisaki
H. Fujii
S. Miwa
Clinical Case Reports Pages: 214 - 215
Inherited pericentric inversion of human chromosome 5
Giusi Barbata
Giuseppina Granata
Paolo Carbone
Cases Observed Pages: 216 - 216
Inducible fragile site on chromosome 3
A. Markkanen
S. Knuutila
A. de la Chapelle
Letters to the Editors Pages: 217 - 217
Reply to the letter of A. Markkanen, S. Knuutila, and A. de la Chapelle
Rolf-Dieter Wegner
Letters to the Editors Pages: 218 - 218
Announcements

Announcement Pages: 219 - 219
Erratum

Erratum Pages: 220 - 220

Volume 65, Issue 2

Increased satellite association induced by 5′ Bromodeoxyuridine treatment of Phytohemaglutinin-stimulated blood lymphocytes

Cystic fibrosis in the Ohio Amish: Gene frequency and founder effect

Effect of oxygen tension on chromosomal aberrations in Fanconi anaemia

A deficiency mutant of the Gc system

Interferon induction of (2′–5′) oligoisoadenylate synthetase in diploid and trisomy 21 human fibroblasts: Relation to dosage of the interferon receptor gene (IRFC)

Complementation analysis in Gaucher disease using single cell microassay techniques. Evidence for a single “Gaucher gene”

A dominantly inherited cytogenetic anomaly: A possible cell division mutant

Familial, EsD-linked, retinoblastoma with reduced penetrance and variable expressivity

Are bowing of long tubular bones and preaxial polydactyly signs of the Meckel syndrome?

Interstitial deletion for a region in the long arm of chromosome 16

The sequence of DNA replication in an iso-dicentric X-chromosome in peripheral blood lymphocytes and skin fibroblasts from the same individual

Methyl green is a substitute for distamycin A in the formation of distamycin A/DAPI C-bands

Glutamate pyruvate transaminase null allele in seven new families

Juvenile idiopathic haemochromatosis: A life-threatening disorder presenting as hypogonadotropic hypogonadism

The genetic significance of accessory bisatellited marker chromosomes

Mating between two balanced translocation carriers in two unrelated families

Genetic linkage relationships between the Xg blood group system and two X chromosome DNA polymorphisms in families with Duchenne and Becker muscular dystrophy

Prenatal diagnosis of Tay-Sachs disease. Reflectometry of hexosaminidase A, B, and C/S bands on zymograms

The polymorphism of the vitamin D-binding protein (Gc); Isoelectric focusing in 3 M urea as additional method for identification of genetic variants

A genetic component of the variance of N-acetoxy-2-acetylaminofluorene-induced DNA damage in mononuclear leukocytes determined by a twin study

Meiotic studies in a series of 1100 infertile and sterile males

On the identity of arylsulphatase C and steroid sulphatase

Protein A radio-assay of H-Y antigen on human leukocytes using mouse and rat antisera and monoclonal antibodies

Chromosomal localization of a human myosin heavy-chain gene by in situ hybridization

Characterization of a human genomic DNA fragment coding for a myosin heavy chain

Four new haplotypes observed in Algerian β-thalassemia patients

Regional localization of the human factor IX gene by molecular hybridization

Sex vesicle loss: A possible explanation of the excess of XO over XXY conceptuses in mice and men

Fragile chromosome 16(q22) cause a balanced translocation at the same point

G6PD Sendagi: A new glucose-6-phosphate dehydrogenase variant associated with congenital hemolytic anemia

Inherited pericentric inversion of human chromosome 5

Inducible fragile site on chromosome 3

Reply to the letter of A. Markkanen, S. Knuutila, and A. de la Chapelle

Announcements

Erratum

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