Volume 87, Issue 5

Search all Human Genetics articles

September 1991

22 articles in this issue

Diagnosis of genetic disease using recombinant DNA. Third edition
D. N. Cooper
J. Schmidtke
Review Article Pages: 519 - 560
Possible mapping of the gene for transient myeloproliferative syndrome at 21q11.2
Norio Niikawa
Han-Xiang Deng
Tadashi Kajii
Original Investigations Pages: 561 - 566
Increased SOD1 enzymatic activity and gene modifications in orangutans: evolutionary implications
Jean de Grouchy
Annie Nicole
Nicole Créau-Goldberg
Original Investigations Pages: 567 - 570
Studies on the phylogenetic conservation of the SRY gene
Terrence R. Tiersch
Michael J. Mitchell
Stephen S. Wachtel
Original Investigations Pages: 571 - 573
Polymorphisms of the gene encoding cholesterol ester transfer protein and serum lipoprotein levels in subjects with and without coronary heart disease
Heli Tenkanen
Pekka Koskinen
Christian Ehnholm
Original Investigations Pages: 574 - 578
A 5′-truncated c-myc gene variant not associated with a risk of cancer
N. S. Pellegata
G. Bergamaschi
G. N. Ranzani
Original Investigations Pages: 579 - 582
“Spontaneous” FRA16B is a hot spot for sister chromatid exchanges
T. Lukusa
E. Meulepas
J. J. Cassiman
Original Investigations Pages: 583 - 586
Two unrelated children with partial trisomy 1q and monosomy 6p, presenting with the phenotype of the Larsen syndrome
G. Pierquin
N. Van Regemorter
E. Vamos
Original Investigations Pages: 587 - 591
Synthesis of glycosaminoglycans in fibroblasts from abortuses with trisomy, triploidy, and from children with Down's syndrome
V. I. Kukharenko
E. M. Pichugina
A. A. Delvig
Original Investigations Pages: 592 - 596
Nucleotide sequence evidence of the unicentric origin of the β^C mutation in Africa
Guy Trabuchet
Jacques Elion
Dominique Labie
Original Investigations Pages: 597 - 601
Analysis of synaptonemal complexes in a heterozygous human male carrier of a reciprocal translocation involving an acrocentric chromosome: heterosynapsis without previous homosynapsis
A. de Perdigo
O. Gabriel-Robez
Y. Rumpler
Original Investigations Pages: 602 - 606
The molecular genetics of haemophilia A: screening for point mutations in the factor VIII gene using the restriction enzyme TaqI
David S. Millar
Barbara Zoll
David N. Cooper
Original Investigations Pages: 607 - 612
Methods for analysis of multiple cystic fibrosis mutations
Ivy S. L. Ng
Robert Pace
Arthur L. Beaudet
Original Investigations Pages: 613 - 617
Chromosomal localization of the human D₃ dopamine receptor gene
Maryvonne Le Coniat
Pierre Sokoloff
Roland Berger
Short Communications Pages: 618 - 620
Regional assignment of the human cell cycle control gene CDC2 to chromosome 10q21 by in situ hybridization
S. A. Nazarenko
N. V. Ostroverhova
N. K. Spurr
Short Comunications Pages: 621 - 622
The gene for the type II (p75) tumor necrosis factor receptor (TNF-RII) is localized on band 1p36.2–p36.3
Oliver Kemper
Josette Derré
Roland Berger
Short Comunications Pages: 623 - 624
Localisation of the gene coding for the haemopoietic stem cell antigen CD34 to chromosome 1q32
Spencer M. Howell
Harald V. Molgaard
Nigel K. Spurr
Short Comunications Pages: 625 - 627
Glutathione S-transferase class μ in French alcoholic cirrhotic patients
Alexis Groppi
Christiane Coutelle
Patrice Couzigou
Short Comunications Pages: 628 - 630
An unusual variant detected using a β-globin probe for an individual with the sickle cell trait
Rohan Taylor
M. Patton
S. Jeffery
OriginalPaper Pages: 631 - 631
DNA-fingerprinting: a short note on mutation rates
Michael Krawczak
Barbara Bockel
Letters to the Editors Pages: 632 - 633
Reply to letter by M. Krawczak and B. Bockel
Jörg T. Epplen
OriginalPaper Pages: 633 - 633
Segregation of lymphocyte low molecular weight DNA and antinuclear antibodies in a family with systemic lupus erythematosus in first cousins
M. A. Fletcher
P. Phillips
P. J. Benke
OriginalPaper Pages: 634 - 634

Volume 87, Issue 5

Diagnosis of genetic disease using recombinant DNA. Third edition

Possible mapping of the gene for transient myeloproliferative syndrome at 21q11.2

Increased SOD1 enzymatic activity and gene modifications in orangutans: evolutionary implications

Studies on the phylogenetic conservation of the SRY gene

Polymorphisms of the gene encoding cholesterol ester transfer protein and serum lipoprotein levels in subjects with and without coronary heart disease

A 5′-truncated c-myc gene variant not associated with a risk of cancer

“Spontaneous” FRA16B is a hot spot for sister chromatid exchanges

Two unrelated children with partial trisomy 1q and monosomy 6p, presenting with the phenotype of the Larsen syndrome

Synthesis of glycosaminoglycans in fibroblasts from abortuses with trisomy, triploidy, and from children with Down's syndrome

Nucleotide sequence evidence of the unicentric origin of the β^C mutation in Africa

Analysis of synaptonemal complexes in a heterozygous human male carrier of a reciprocal translocation involving an acrocentric chromosome: heterosynapsis without previous homosynapsis

The molecular genetics of haemophilia A: screening for point mutations in the factor VIII gene using the restriction enzyme TaqI

Methods for analysis of multiple cystic fibrosis mutations

Chromosomal localization of the human D₃ dopamine receptor gene

Regional assignment of the human cell cycle control gene CDC2 to chromosome 10q21 by in situ hybridization

The gene for the type II (p75) tumor necrosis factor receptor (TNF-RII) is localized on band 1p36.2–p36.3

Localisation of the gene coding for the haemopoietic stem cell antigen CD34 to chromosome 1q32

Glutathione S-transferase class μ in French alcoholic cirrhotic patients

An unusual variant detected using a β-globin probe for an individual with the sickle cell trait

DNA-fingerprinting: a short note on mutation rates

Reply to letter by M. Krawczak and B. Bockel

Segregation of lymphocyte low molecular weight DNA and antinuclear antibodies in a family with systemic lupus erythematosus in first cousins

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