Volume 99, Issue 3

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February 1997

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25 articles in this issue

A human UPD-GalNAc: polypeptide, N-acetylgalactosaminyltranferase type 1 gene is located at the chromosomal region 18q12.1
Setsuo Takai
Yuji Hinoda
M. Oshima
Original investigation Pages: 293 - 294
The mapping and visual ordering of the human syndecan-1 and N-myc genes near the telomeric region of chromosome 2p
Jaakko Kaukonen
Leena Alanen-Kurki
A. Palotie
Original investigation Pages: 295 - 297
An extension of the admixture test for the study of genetic heterogeneity in hereditary multiple exostoses
Laurence Legeai-Mallet
Patricia Margaritte-Jeannin
Françoise Clerget-Darpoux
Original investigation Pages: 298 - 302
Close physical linkage of the genes encoding the pNR-2/pS2 protein and human spasmolytic protein (hSP)
F. E. B. May
Bruce R. Westley
Original investigation Pages: 303 - 307
Rapid antibody test for diagnosing fragile X syndrome: a validation of the technique
R. Willemsen
Arie Smits
B. A. Oostra
Original investigation Pages: 308 - 311
DNA multiallelic systems reveal gene/longevity associations not detected by diallelic systems. The APOB locus
G. De Benedictis
E. Falcone
C. Franceschi
Original investigation Pages: 312 - 318
Laryngeal and oropharyngeal cancer, and alcohol dehydrogenase 3 and glutathione S-transferase M1 polymorphisms
C. Coutelle
P. J. Ward
A. Cassaigne
Original investigation Pages: 319 - 325
Mapping of the human adenosine A_2a receptor gene: relationship to potential schizophrenia loci on chromosome 22q and exclusion from the CATCH 22 region
J. Deckert
Markus M. Nöthen
Peter Propping
Original investigation Pages: 326 - 328
Isolation of a cDNA encoding the human homolog of COX17, a yeast gene essential for mitochondrial copper recruitment
Ravi Amaravadi
D. Moira Glerum
A. Tzagoloff
Original investigation Pages: 329 - 333
The human homolog of the rodent immediate early response genes, PC4 and TIS7, resides in the lung cancer tumor suppressor gene region on chromosome 3p21
F. Latif
Fuh-Mei Duh
Michael I. Lerman
Original investigation Pages: 334 - 341
Differential loss of heterozygosity in familial, sporadic, and uremic hyperparathyroidism
F. Farnebo
Bin Tean Teh
Catharina Larsson
Original investigation Pages: 342 - 349
A C57BL/KsJ mouse model of Niemann-Pick disease (spm) belongs to the same complementation group as the major childhood type of Niemann-Pick disease type C
S. Akaboshi
Tamami Yano
Kenzo Takeshita
Original investigation Pages: 350 - 353
Southern analysis for detection of CAG repeat expansions associated with dentatorubral pallidoluysian atrophy
R. L. Alford
R. L. Margolis
C. S. Richards
Original investigation Pages: 354 - 356
Interethnic polymorphism of EWS intron 6: genome plasticity mediated by Alu retroposition and recombination
Jessica Zucman-Rossi
Mark A. Batzer
Gilles Thomas
Original investigation Pages: 357 - 363
Rapid detection of trisomy 21 by homologous gene quantitative PCR (HGQ-PCR)
Hsien-Hsiung Lee
Jan-Gowth Chang
Heung-Tat Ng
Original investigation Pages: 364 - 367
Genomic organization and chromosomal localization of the human casein gene family
Y. Fujiwara
M. Miwa
M. Ueda
Original investigation Pages: 368 - 373
High-resolution comparative hybridization to combed DNA fibers
Jürgen Kraus
Ruthild G. Weber
Thomas Cremer
Original investigation Pages: 374 - 380
Molecular basis of α-thalassemia in Sicily
Marco Fichera
Angela Spalletta
A. Ragusa
Original investigation Pages: 381 - 386
Cloning a new human gene from chromosome 21q22.3 encoding a glutamic acid-rich protein expressed in heart and skeletal muscle
P. Scartezzini
Aliana Egeo
Alberto Rasore-Quartino
Original investigation Pages: 387 - 392
Human orosomucoid polymorphism: molecular basis of the three common ORM1 alleles, ORM1*F1, ORM1*F2, and ORM1*S
I. Yuasa
Kazuo Umetsu
Yoshito Irizawa
Original investigation Pages: 393 - 398
Coding versus intron variability: extremely polymorphic HLA-DRB1 exons are flanked by specific composite microsatellites, even in distant populations
C. Epplen
Eduardo J. M. Santos
Jörg T. Epplen
Original investigation Pages: 399 - 406
Meiotic behaviour of sex chromosomes investigated by three-colour FISH on 35 142 sperm nuclei from two 47,XYY males
E. Chevret
S. Rousseaux
B. Sèle
Rapid communication Pages: 407 - 412
Increased incidence of disomic sperm nuclei in a 47,XYY male assessed by fluorescent in situ hybridization (FISH)
Joan Blanco
Carmen Rubio
F. Vidal
Rapid communication Pages: 413 - 416
Suggestive evidence for linkage of schizophrenia to markers on chromosome 13 in Caucasian but not Oriental populations
M.-W. Lin
P. Sham
John F. Powell
Rapid communication Pages: 417 - 420
Whither Down syndrome critical regions?
Burton L. Shapiro
Rapid communication Pages: 421 - 423

Volume 99, Issue 3

A human UPD-GalNAc: polypeptide, N-acetylgalactosaminyltranferase type 1 gene is located at the chromosomal region 18q12.1

The mapping and visual ordering of the human syndecan-1 and N-myc genes near the telomeric region of chromosome 2p

An extension of the admixture test for the study of genetic heterogeneity in hereditary multiple exostoses

Close physical linkage of the genes encoding the pNR-2/pS2 protein and human spasmolytic protein (hSP)

Rapid antibody test for diagnosing fragile X syndrome: a validation of the technique

DNA multiallelic systems reveal gene/longevity associations not detected by diallelic systems. The APOB locus

Laryngeal and oropharyngeal cancer, and alcohol dehydrogenase 3 and glutathione S-transferase M1 polymorphisms

Mapping of the human adenosine A_2a receptor gene: relationship to potential schizophrenia loci on chromosome 22q and exclusion from the CATCH 22 region

Isolation of a cDNA encoding the human homolog of COX17, a yeast gene essential for mitochondrial copper recruitment

The human homolog of the rodent immediate early response genes, PC4 and TIS7, resides in the lung cancer tumor suppressor gene region on chromosome 3p21

Differential loss of heterozygosity in familial, sporadic, and uremic hyperparathyroidism

A C57BL/KsJ mouse model of Niemann-Pick disease (spm) belongs to the same complementation group as the major childhood type of Niemann-Pick disease type C

Southern analysis for detection of CAG repeat expansions associated with dentatorubral pallidoluysian atrophy

Interethnic polymorphism of EWS intron 6: genome plasticity mediated by Alu retroposition and recombination

Rapid detection of trisomy 21 by homologous gene quantitative PCR (HGQ-PCR)

Genomic organization and chromosomal localization of the human casein gene family

High-resolution comparative hybridization to combed DNA fibers

Molecular basis of α-thalassemia in Sicily

Cloning a new human gene from chromosome 21q22.3 encoding a glutamic acid-rich protein expressed in heart and skeletal muscle

Human orosomucoid polymorphism: molecular basis of the three common ORM1 alleles, ORM1F1, ORM1F2, and ORM1*S

Coding versus intron variability: extremely polymorphic HLA-DRB1 exons are flanked by specific composite microsatellites, even in distant populations

Meiotic behaviour of sex chromosomes investigated by three-colour FISH on 35 142 sperm nuclei from two 47,XYY males

Increased incidence of disomic sperm nuclei in a 47,XYY male assessed by fluorescent in situ hybridization (FISH)

Suggestive evidence for linkage of schizophrenia to markers on chromosome 13 in Caucasian but not Oriental populations

Whither Down syndrome critical regions?

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