Volume 74, Issue 4

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December 1986

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29 articles in this issue

Localization of the LDHA gene to 11p14→11p15 by in situ hybridization of an LDHA cDNA probe to two translocations with breakpoints in 11p13
T. L. Yang-Feng
G. A. P. Bruns
U. Francke
Original Investigations Pages: 331 - 334
In vivo chromosomal instability in ataxia-telangiectasia homozygotes and heterozygotes
Miriam P. Rosin
H. D. Ochs
Original Investigations Pages: 335 - 340
The plasminogen polymorphism in South African Negro populations: genetics and anthropogenetics
H. W. Hitzeroth
Ulrike Skoda
G. Mauff
Original Investigations Pages: 341 - 345
Detection of chromosome aberrations in the human interphase nucleus by visualization of specific target DNAs with radioactive and non-radioactive in situ hybridization techniques: diagnosis of trisomy 18 with probe L1.84
T. Cremer
J. Landegent
M. van der Ploeg
Original Investigations Pages: 346 - 352
Measurements of the frequency of human erythrocytes with gene expression loss phenotypes at the glycophorin A locus
R. G. Langlois
W. L. Bigbee
R. H. Jensen
Original Investigations Pages: 353 - 362
Abnormal electrophoretic mobility of spectrin tetramers in hereditary elliptocytosis
D. Dhermy
M. Garbarz
P. Boivin
Original Investigations Pages: 363 - 367
An elongated segment of DNA observed between two human α globin genes
T. Nakatsuji
H. Landman
T. H. J. Huisman
Original Investigations Pages: 368 - 371
Molecular detection of a translocation (Y;15) in a 45,X male
C. M. Disteche
L. Brown
D. C. Page
Original Investigations Pages: 372 - 377
Assignment of human transcobalamin II (TC2) to chromosome 22 using somatic cell hybrids and monosomic meningioma cells
F. Arwert
H. J. Porck
A. W. Eriksson
Original Investigations Pages: 378 - 381
Congenital malformations and genetic diseases in Iranian infants
D. D. Farhud
Gh. -R. Walizadeh
M. Sharif Kamali
Original Investigations Pages: 382 - 385
Severe short-limb dwarfism resembling Grebe chondrodysplasia
Ahmad S. Teebi
Sadika A. Al-Awadi
J. Spranger
Original Investigations Pages: 386 - 390
Localisation of the gene for Hunter syndrome on the long arm of X chromosome
M. Upadhyaya
M. Sarfarazi
P. S. Harper
Original Investigations Pages: 391 - 398
Chromosome studies in 2136 couples with spontaneous abortions
G. Bourrouillou
P. Colombies
N. Dastugue
Original Investigations Pages: 399 - 401
Associations between restriction fragment length polymorphisms detected with a probe for human 21-hydroxylase (21-OH) and two clinical forms of 21-OH deficiency
E. Mornet
P. Couillin
J. Dausset
Original Investigations Pages: 402 - 408
A linkage study of Emery-Dreifuss muscular dystrophy
Shirley Hodgson
Ernst Boswinkel
M. Bobrow
Original Investigations Pages: 409 - 416
Partial trisomy 20p resulting from a recombination of a familial pericentric inversion
N. Bown
I. Cross
J. Burn
Original Investigations Pages: 417 - 419
Localization of the gene for human erythrocyte glycophorin C to chromosome 2, q14–q21
M. G. Mattei
Y. Colin
J. P. Cartron
Original Investigations Pages: 420 - 422
New regional localisations for HAGH and PGP on human chromosome 16
J. C. Mulley
D. F. Callen
Original Investigations Pages: 423 - 424
A highly polymorphic locus on chromosome 16q revealed by a probe from a chromosome-specific cosmid library
L. Bufton
T. K. Mohandas
M. Litt
Original Investigations Pages: 425 - 431
Alpha-thalassemia in Papua New Guinea
P. Yenchitsomanus
K. M. Summers
G. T. Nurse
Original Investigations Pages: 432 - 437
Oxygen-induced cytogenetic instability in normal human lymphocytes
H. Joenje
Anneke B. Oostra
Original Investigations Pages: 438 - 440
Prematurely condensed human sperm chromosomes after in vitro fertilization (IVF)
H. Schmiady
K. Sperling
M. Stauber
Original Investigations Pages: 441 - 443
The effect of 1-β-d-arabinofuranosyl-cytosine on the expression of the common fragile site at 3p14
Xinzhi Li
Zu-an Yan
Xianting Zhou
Original Investigations Pages: 444 - 446
Aberrant breakpoints in chronic myelogenous leukaemia; oncogenes and fragile sites
J. L. Huret
J. Tanzer
M. Henry-Amar
Original Investigations Pages: 447 - 448
Choroideremia: further evidence for assignment of the locus to Xq13–Xq21
Marianne Schwartz
T. Rosenberg
L. U. Lamm
Original Investigations Pages: 449 - 452
Cell culture studies on neurofibromatosis (von Recklinghausen)
Winfrid Krone
Inge Högemann
Short Communications Pages: 453 - 455
Origin of new mutations in Duchenne muscular dystrophy
Laura Roncuzzi
Alessandra Ferlini
G. Romeo
Short Communications Pages: 456 - 460
Mid-trimester ultrasonographic diagnosis of early manifesting “adult” form of polycystic kidney disease
J. P. Fryns
K. Vandenberghe
F. Moerman
Letters to the Editors Pages: 461 - 461
Announcements

Announcement Pages: 462 - 462

Volume 74, Issue 4

Localization of the LDHA gene to 11p14→11p15 by in situ hybridization of an LDHA cDNA probe to two translocations with breakpoints in 11p13

In vivo chromosomal instability in ataxia-telangiectasia homozygotes and heterozygotes

The plasminogen polymorphism in South African Negro populations: genetics and anthropogenetics

Detection of chromosome aberrations in the human interphase nucleus by visualization of specific target DNAs with radioactive and non-radioactive in situ hybridization techniques: diagnosis of trisomy 18 with probe L1.84

Measurements of the frequency of human erythrocytes with gene expression loss phenotypes at the glycophorin A locus

Abnormal electrophoretic mobility of spectrin tetramers in hereditary elliptocytosis

An elongated segment of DNA observed between two human α globin genes

Molecular detection of a translocation (Y;15) in a 45,X male

Assignment of human transcobalamin II (TC2) to chromosome 22 using somatic cell hybrids and monosomic meningioma cells

Congenital malformations and genetic diseases in Iranian infants

Severe short-limb dwarfism resembling Grebe chondrodysplasia

Localisation of the gene for Hunter syndrome on the long arm of X chromosome

Chromosome studies in 2136 couples with spontaneous abortions

Associations between restriction fragment length polymorphisms detected with a probe for human 21-hydroxylase (21-OH) and two clinical forms of 21-OH deficiency

A linkage study of Emery-Dreifuss muscular dystrophy

Partial trisomy 20p resulting from a recombination of a familial pericentric inversion

Localization of the gene for human erythrocyte glycophorin C to chromosome 2, q14–q21

New regional localisations for HAGH and PGP on human chromosome 16

A highly polymorphic locus on chromosome 16q revealed by a probe from a chromosome-specific cosmid library

Alpha-thalassemia in Papua New Guinea

Oxygen-induced cytogenetic instability in normal human lymphocytes

Prematurely condensed human sperm chromosomes after in vitro fertilization (IVF)

The effect of 1-β-d-arabinofuranosyl-cytosine on the expression of the common fragile site at 3p14

Aberrant breakpoints in chronic myelogenous leukaemia; oncogenes and fragile sites

Choroideremia: further evidence for assignment of the locus to Xq13–Xq21

Cell culture studies on neurofibromatosis (von Recklinghausen)

Origin of new mutations in Duchenne muscular dystrophy

Mid-trimester ultrasonographic diagnosis of early manifesting “adult” form of polycystic kidney disease

Announcements

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