Volume 97, Issue 6

Search all Human Genetics articles

May 1996

29 articles in this issue

H-Y antigens
U. Müller
Review Article Pages: 701 - 704
Interstitial deletion of chromosome 6q: Precise definition of the breakpoints by microdissection, DNA amplification, and reverse painting
N. Rubtsov
G. Senger
H. Kuzcera
Original Investigation Pages: 705 - 709
Extreme variant of the short arm of chromosome 15
U. Friedrich
A. J. Therkelsen
E. Niebuhr
Original Investigation Pages: 710 - 713
Allelic association between a Ser-9-Gly polymorphism in the dopamine D3 receptor gene and schizophrenia
S. Shaikh
D. A. Collier
M. Gill
Original Investigation Pages: 714 - 719
Localization of the humanRGR opsin gene to chromosome 10q23
X. -N. Chen
J. R. Korenberg
H. K. W. Fong
Original Investigation Pages: 720 - 722
Novel interleukin-1 receptor antagonist exon polymorphisms and their use in allele-specific mRNA assessment
F. E. Clay
J. K. Tarlow
G. W. Duff
Original Investigation Pages: 723 - 726
Geographic distribution and origin of CFTR mutations in Germany
B. Tümmler
T. Storrs
X. Estivill
Original Investigation Pages: 727 - 731
Genetic mapping studies of 40 loci and 23 cosmids in chromosome 11p13-11g13, and exclusion of μ-calpain as the multiple endocrine neoplasia type 1 gene
J. T. Pang
S. E. Lloyd
R. T. Taggart
Original Investigation Pages: 732 - 741
EagI andNotI linking clones from human chromosomes 11 and Xp
Mark A. Pook
Rekhaben Thakrar
Rajesh V. Thakker
Original Investigation Pages: 742 - 749
Accelerated loss of telomeric repeats may not explain accelerated replicative decline of Werner syndrome cells
V. P. Schulz
V. A. Zakian
S. D. Edland
Original Investigation Pages: 750 - 754
Hereditary ceruloplasmin deficiency with hemosiderosis
N. Okamoto
S. Wada
Y. Wada
Original Investigation Pages: 755 - 758
Distribution and frequency of a polymorphicAlu insertion at the plasminogen activator locus in humans
S. A. Tishkoff
G. Ruano
K. K. Kidd
Original Investigation Pages: 759 - 764
Isolation of the human chromosome 22q telomere and its application to detection of cryptic chromosomal abnormalities
Yi Ning
Marjorie Rosenberg
Leslie G. Biesecker
Original Investigation Pages: 765 - 769
Detection of a germline mutation and somatic homozygous loss of the von Hippel-Lindau tumor-suppressor gene in a family with a de novo mutation
Hans-Jochen H. Decker
Christine Neuhaus
Christoph Huber
Original Investigation Pages: 770 - 776
Extensive polymorphism of ABO blood group gene: three major lineages of the alleles for the common ABO phenotypes
Kenichi Ogasawara
Makoto Bannai
Katsushi Tokunaga
Original Investigation Pages: 777 - 783
Routine screening for microdeletions by FISH in 77 patients suspected of having Prader-Willi or Angelman syndromes using YAC clone 273A2 (D15S10)
M. Erdel
S. Köchl
U. Barth-Witte
Original Investigation Pages: 784 - 793
Localization of the human vascular endothelial growth factor gene,VEGF, at Chromosome 6p12
M. -H. Wei
N. C. Popescu
M. J. Merrill
Original Investigation Pages: 794 - 797
Evidence of genetic heterogeneity of Leber's congenital amaurosis (LCA) and mapping of LCA1 to chromosome 17p13
A. Camuzat
J. -M. Rozet
J. Weissenbach
Original Investigation Pages: 798 - 801
Familial double pericentric inversion of chromosome 5 with some features of cri-du-chat syndrome
Sheryl A. Goodart
Merlin G. Butler
Joan Overhauser
Original Investigation Pages: 802 - 807
A PCR-based test suitable for screening for fragile X syndrome among mentally retarded males
Luciana A. Haddad
Regina C. Mingroni-Netto
Sérgio D. J. Pena
Original Investigation Pages: 808 - 812
Allele-specific quantification of TNFA transcripts in rheumatoid arthritis
Brigitta M. N. Brinkman
Tom W. J. Huizinga
Cornelis L. Verweij
Original Investigation Pages: 813 - 818
The effect of Y-chromosome alpha-satellite array length on the rate of sex chromosome disomy in human sperm
Michael A. Abruzzo
Darren K. Griffin
Terry J. Hassold
Original Investigation Pages: 819 - 823
A family segregating a Friedreich ataxia phenotype that is not linked to the FRDA locus
Patricia Smeyers
Eugènia Monrós
Francesc Palau
Original Investigation Pages: 824 - 828
Hb Costa Rica or α₂β₂77(EF1)His→Arg: The first example of a somatic cell mutation in a globin gene
W. E. Rodriguez Romero
M. Castillo
T. H. J. Huisman
Original Investigation Pages: 829 - 833
Allelic loss of the short arm of chromosome 4 in neuroblastoma suggests a novel tumour suppressor gene locus
Huib Caron
Peter van Sluis
Rogier Versteeg
Original Investigation Pages: 834 - 837
A novel 5′-upstream mutation in the factor X11 gene is associated with a Taql restriction site in an Alu repeat in factor X11-deficient patients
Sigrun Hofferbert
Jens Müller
Manfred Schloesser
Rapid Communication Pages: 838 - 841
Six new polymorphic microsatellite markers used for the integration of genetic and physical maps of human chromosome 7
Simone Beck
Farah Badbanchi
Karl-Heinz Grzeschik
Rapid Communication Pages: 842 - 844
Announcements

Announcement Pages: 845 - 845
Hb Costa Rica or · ₂ ‚ ₂77(EF1)His→Arg: the first example of a somatic cell mutation in a globin gene
W. E. Rodriguez Romero
M. Castillo
T. H. J. Huisman
Original investigation Pages: 829 - 833

Volume 97, Issue 6

H-Y antigens

Interstitial deletion of chromosome 6q: Precise definition of the breakpoints by microdissection, DNA amplification, and reverse painting

Extreme variant of the short arm of chromosome 15

Allelic association between a Ser-9-Gly polymorphism in the dopamine D3 receptor gene and schizophrenia

Localization of the humanRGR opsin gene to chromosome 10q23

Novel interleukin-1 receptor antagonist exon polymorphisms and their use in allele-specific mRNA assessment

Geographic distribution and origin of CFTR mutations in Germany

Genetic mapping studies of 40 loci and 23 cosmids in chromosome 11p13-11g13, and exclusion of μ-calpain as the multiple endocrine neoplasia type 1 gene

EagI andNotI linking clones from human chromosomes 11 and Xp

Accelerated loss of telomeric repeats may not explain accelerated replicative decline of Werner syndrome cells

Hereditary ceruloplasmin deficiency with hemosiderosis

Distribution and frequency of a polymorphicAlu insertion at the plasminogen activator locus in humans

Isolation of the human chromosome 22q telomere and its application to detection of cryptic chromosomal abnormalities

Detection of a germline mutation and somatic homozygous loss of the von Hippel-Lindau tumor-suppressor gene in a family with a de novo mutation

Extensive polymorphism of ABO blood group gene: three major lineages of the alleles for the common ABO phenotypes

Routine screening for microdeletions by FISH in 77 patients suspected of having Prader-Willi or Angelman syndromes using YAC clone 273A2 (D15S10)

Localization of the human vascular endothelial growth factor gene,VEGF, at Chromosome 6p12

Evidence of genetic heterogeneity of Leber's congenital amaurosis (LCA) and mapping of LCA1 to chromosome 17p13

Familial double pericentric inversion of chromosome 5 with some features of cri-du-chat syndrome

A PCR-based test suitable for screening for fragile X syndrome among mentally retarded males

Allele-specific quantification of TNFA transcripts in rheumatoid arthritis

The effect of Y-chromosome alpha-satellite array length on the rate of sex chromosome disomy in human sperm

A family segregating a Friedreich ataxia phenotype that is not linked to the FRDA locus

Hb Costa Rica or α₂β₂77(EF1)His→Arg: The first example of a somatic cell mutation in a globin gene

Allelic loss of the short arm of chromosome 4 in neuroblastoma suggests a novel tumour suppressor gene locus

A novel 5′-upstream mutation in the factor X11 gene is associated with a Taql restriction site in an Alu repeat in factor X11-deficient patients

Six new polymorphic microsatellite markers used for the integration of genetic and physical maps of human chromosome 7

Announcements

Hb Costa Rica or · ₂ ‚ ₂77(EF1)His→Arg: the first example of a somatic cell mutation in a globin gene

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