Volume 39 Issue 4, December 1994

DNA fingerprinting involving fluorescence-labeled termini of any enzymatically generated fragments of DNA

• Xiaoren Tang
• Yifei Wang
• Kazushige Yokoyama

Genomic structure and chromosomal localization of processed pseudogenes for human RBP-J_k

• Mingdi Zhang
• Xiaoren Tang
• Kazushige Yokoyama

Carrier detection of Werner's syndrome using a microsatellite that exhibits linkage disequilibrium with the Werner's syndrome locus

• Koichi Kihara
• Jun Nakura
• Toshio Ogihara

Isolation of human chromosome 21-specific cosmids and their uses in mapping of cosmid contigs on chromosomal subregions

• De-Xing Hou
• Haruo Kishida
• Eiichi Soeda

Direct mapping of the human TATA box-binding protein (TBP) gene to 6q27 by fluorescencein situ hybridization

• Fumiko Saito
• Tohru Yamamoto
• Tatsuro Ikeuchi

The attitude of Japanese physicians regarding genetic service for autosomal dominant polycystic kidney disease (ADPKD)

• Shinsuke Nomura
• Shin-ichiro Kawai
• Gengo Osawa

Chromosome 1q terminal deletion resulting fromde novo translocation with an acrocentric chromosome

• Eiko Arai
• Shuichi Nishimura
• Tatsuro Ikeuchi

Identification of a single base polymorphism in intron 2 of the c-fos gene and its detection by mismatched PCR-RFLP

• Kouzin Kamino
• Tetsuro Miki
• Toshio Ogihara

Dinucleotide repeat polymorphism at the D8S1055

• Lin Ye
• Koichi Kihara
• Toshio Ogihara

Dinucleotide repeat polymorphism at the D8S1053

• Jun Nakura
• Lin Ye
• Toshio Ogihara

Six dinucleotide repeat polymorphisms on chromosome 7

• Jun Nakura
• Tetsuro Miki
• Yoshizumi Ishino

An apparent balanced translocation between chromosomes 7 and 13 [t(7;13) (p15;q32)] in a 47,XYY individual

• Ram S. Verma
• Radha Giridharan
• Sunny Luke

Essential medical genetics

• J. M. Connor
• M. A. Ferguson-Smith

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