Physical Mapping of a Translocation Breakpoint in Neurofibromatosis-Reference-Cited by-同舟云学术

Physical Mapping of a Translocation Breakpoint in Neurofibromatosis

Published:1989-06-02 Issue:4908 Volume:244 Page:1085-1087
ISSN:0036-8075
Container-title:Science
language:en
Short-container-title:Science

Author:

Fountain Jane W.¹,Wallace Margaret R.¹,Bruce Melissa A.¹,Seizinger Bernd R.²,Menon Anil G.²,Gusella James F.²,Michels Virginia V.³,Schmidt Michael A.³,Dewald Gordon W³,Collins Francis S.¹

Affiliation:

1. Departments of Internal Medicine and Human Genetics, University of Michigan, Ann Arbor, MI 48109.

2. Neurogenetics Laboratory, Massachusetts General Hospital, Boston, MA 02114.

3. Mayo Clinic, Rochester, MN 55905.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

Reference31 articles.

1. Gene for von Recklinghausen Neurofibromatosis Is in the Pericentromeric Region of Chromosome 17

2. CpG-rich islands and the function of DNA methylation

3. Electrophoretic Separations of Large DNA Molecules by Periodic Inversion of the Electric Field

4. COLLINS, F.S., THE VON RECKLINGHAUSEN NEUROFIBROMATOSIS REGION ON CHROMOSOME 17-GENETIC AND PHYSICAL MAPS COME INTO FOCUS, AMERICAN JOURNAL OF HUMAN GENETICS 44: 1 (1989).

5. A Clinical Pathological and Genetic Study of Multiple NeUrofibromatosis 1956

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