Initial sequencing and analysis of the human genome.
Eric S. Lander;Lauren M. Linton;Bruce Birren;Chad Nusbaum.
Human Homolog of patched, a Candidate Gene for the Basal Cell Nevus Syndrome
Ronald L. Johnson;Alana L. Rothman;Jingwu Xie;Lisa V. Goodrich.
A gene map of the human genome
G. D. Schuler;M. S. Boguski;E. A. Stewart;L. D. Stein.
An Apolipoprotein Influencing Triglycerides in Humans and Mice Revealed by Comparative Sequencing
Len A. Pennacchio;Michael Olivier;Jaroslav A. Hubacek;Jonathan C. Cohen.
Structure and variability of human chromosome ends.
T de Lange;L Shiue;R M Myers;D R Cox.
Molecular and Cellular Biology (1990)
Mode of proviral activation of a putative mammary oncogene ( int -1) on mouse chromosome 15
R. Nusse;A. Van Ooyen;D. Cox;Y. K. T. Fung.
Radiation hybrid mapping: a somatic cell genetic method for constructing high-resolution maps of mammalian chromosomes
David R. Cox;Margit Burmeister;E. Roydon Price;Suwon Kim.
A physical map of the human genome.
John Douglas Mcpherson;Marco Marra;Marco Marra;La Deana Hillier;Robert H. Waterston.
A potassium channel mutation in weaver mice implicates membrane excitability in granule cell differentiation.
Nila Patil;David R. Cox;Deepti Bhat;Malek Faham.
Nature Genetics (1995)
Mutations in the Gene Encoding Cystatin B in Progressive Myoclonus Epilepsy (EPM1)
Len A. Pennacchio;Anna-Elina Lehesjoki;Nancy E. Stone;Virginia L. Willour.
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