Volume 53, Issue 1

Search all Human Genetics articles

December 1979

25 articles in this issue

Omphalocele and partial trisomy 1q syndrome
H. Chen
J. J. Gershanik
I. D. Sanusi
Original Investigations Pages: 1 - 4
Chromosomes in acute leukemia
E. L. Prigogina
E. W. Fleischman
I. S. Peterson
Original Investigations Pages: 5 - 16
Segregation of rat chromosomes in somatic cell hybrids between rat cells and HT 1080 human fibrosarcoma cells
G. G. D'Ancona
C. M. Croce
Original Investigations Pages: 17 - 21
Heritable fragile sites on human chromosomes
G. R. Sutherland
Original Investigations Pages: 23 - 27
Heritable fragile sites on human chromosomes
G. R. Sutherland
P. Leonard
Original Investigations Pages: 29 - 30
Genetic studies of complement C4 in man
G. B. Petersen
Inger Juncker Sørensen
L. U. Lamm
Original Investigations Pages: 31 - 36
Hurler-Scheie phenotype: A report of two pairs of inbred sibs
N. Kaibara
M. Eguchi
K. Takagishi
Original Investigations Pages: 37 - 41
Characterization of some erythrocyte G6PD variants by isoelectric focusing
H. Vergnes
H. Brun
Original Investigations Pages: 43 - 45
Assignment of a gene for human quinoid-dihydropteridine reductase (QDPR, EC 1.6.5.1) to chromosome 4
P. Kuhl
K. Olek
K. -H. Grzeschik
Original Investigations Pages: 47 - 49
H-Y antigen in Swyer syndrome and the genetics of XY gonadal dysgenesis
C. A. Moreira-Filho
S. P. A. Toledo
A. Wajntal
Original Investigations Pages: 51 - 56
H-Y antigen-positive male pseudohermaphroditism with 45,X/46,XYq-mosaicism
J. B. Maihes
D. E. Pittaway
W. D. Grafton
Original Investigations Pages: 57 - 63
X-Linked dominant chondrodysplasia punctata
R. Happle
Original Investigations Pages: 65 - 73
Qualitative and quantitative study of the growth and cell surface properties of Huntington's disease fibroblasts and age-matched controls
J. J. Cassiman
J. Verlinden
H. Van den Berghe
Original Investigations Pages: 75 - 86
Human alcohol dehydrogenase ADH₂ and ADH₃ polymorphisms in ethnic Chinese and Indians of West Malaysia
Y. -S. Teng
S. Jehan
L. E. Lie-Injo
Original Investigations Pages: 87 - 90
Characterization of alpha-1-antitrypsin by isoelectric focusing on an ultrathin polyacrylamide gel layer
G. Massi
A. Fabiano
P. Auconi
Original Investigations Pages: 91 - 95
Improved screening test for abnormal hemoglobins from dried blood samples
K. Altland
M. Kaempfer
H. Granda
Original Investigations Pages: 97 - 100
Gm allotypes and racial admixture in two Brazilian populations
H. Schneider
F. M. Salzano
Original Investigations Pages: 101 - 105
Demonstration of Y/autosomal translocations using distamycin A
M. Schmid
Short Communications Pages: 107 - 109
A new translocation in Burkitt's tumor cells
R. Berger
A. Bernheim
N. Colbert
Short Communications Pages: 111 - 112
Failure to demonstrate abnormal lymphocyte capping in humans, mice and hamsters with muscular dystrophy
M. E. Gershwin
R. G. Taylor
Barbara Finlayson
Short Communications Pages: 113 - 114
Deficiency of arylsulfatase C in cultured skin fibroblasts of X-linked ichthyosis
J. Ch. Meyer
H. Weiss
U. W. Schnyder
Short Communications Pages: 115 - 116
Pericentric inversion in chromosome No.2 as a de novo mutation
Ulla Hesselbjerg
Ursula Friedrich
Clinical Case Reports Pages: 117 - 119
Partial trisomy 7q and probable partial monosomy of 5p in the son of a mother with a reciprocal translocation between 5p and 7q
A. Schinzel
O. Tönz
Clinical Case Reports Pages: 121 - 124
Familial transmission of a translocation Y/14
C. H. C. M. Buys
G. J. P. A. Anders
A. Y. van der Hoek-van der Veen
Clinical Case Reports Pages: 125 - 127
Exclusion of the localization of the Gm, Pi, and C3 genes on 6q25→6qter through blood group analysis of the patients of Schmid, D'Apuzzo and rossi (Hum. Genet. 46, 279–284, 1979)
K. Bender
K. Burckhardt
K. Schroetter
Letters to the Editors Pages: 129 - 130

Volume 53, Issue 1

Omphalocele and partial trisomy 1q syndrome

Chromosomes in acute leukemia

Segregation of rat chromosomes in somatic cell hybrids between rat cells and HT 1080 human fibrosarcoma cells

Heritable fragile sites on human chromosomes

Heritable fragile sites on human chromosomes

Genetic studies of complement C4 in man

Hurler-Scheie phenotype: A report of two pairs of inbred sibs

Characterization of some erythrocyte G6PD variants by isoelectric focusing

Assignment of a gene for human quinoid-dihydropteridine reductase (QDPR, EC 1.6.5.1) to chromosome 4

H-Y antigen in Swyer syndrome and the genetics of XY gonadal dysgenesis

H-Y antigen-positive male pseudohermaphroditism with 45,X/46,XYq-mosaicism

X-Linked dominant chondrodysplasia punctata

Qualitative and quantitative study of the growth and cell surface properties of Huntington's disease fibroblasts and age-matched controls

Human alcohol dehydrogenase ADH₂ and ADH₃ polymorphisms in ethnic Chinese and Indians of West Malaysia

Characterization of alpha-1-antitrypsin by isoelectric focusing on an ultrathin polyacrylamide gel layer

Improved screening test for abnormal hemoglobins from dried blood samples

Gm allotypes and racial admixture in two Brazilian populations

Demonstration of Y/autosomal translocations using distamycin A

A new translocation in Burkitt's tumor cells

Failure to demonstrate abnormal lymphocyte capping in humans, mice and hamsters with muscular dystrophy

Deficiency of arylsulfatase C in cultured skin fibroblasts of X-linked ichthyosis

Pericentric inversion in chromosome No.2 as a de novo mutation

Partial trisomy 7q and probable partial monosomy of 5p in the son of a mother with a reciprocal translocation between 5p and 7q

Familial transmission of a translocation Y/14

Exclusion of the localization of the Gm, Pi, and C3 genes on 6q25→6qter through blood group analysis of the patients of Schmid, D'Apuzzo and rossi (Hum. Genet. 46, 279–284, 1979)

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