Implications of FRA16A Structure for the Mechanism of Chromosomal Fragile Site Genesis-Reference-Cited by-同舟云学术

Implications of FRA16A Structure for the Mechanism of Chromosomal Fragile Site Genesis

Published:1994-06-24 Issue:5167 Volume:264 Page:1938-1941
ISSN:0036-8075
Container-title:Science
language:en
Short-container-title:Science

Author:

Nancarrow J. K.¹,Kremer E.¹,Holman K.¹,Eyre H.¹,Doggett N. A.²,Le Paslier D.³,Callen D. F.¹,Sutherland G. R.¹,Richards R. I.¹

Affiliation:

1. Centre for Medical Genetics, Department of Cytogenetics and Molecular Genetics, Women's and Children's Hospital, North Adelaide, South Australia 5006, Australia.

2. Center for Human Genome Studies and Life Sciences Division, Los Alamos National Laboratory, Los Alamos, NM 87545, USA.

3. Centre d'Etude du Polymorphisme Humain, F-7501 01, Paris, France.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

Reference30 articles.

1. ASHIZAWA, T, CHARACTERISTICS OF INTERGENERATIONAL CONTRACTIONS OF THE CTG REPEAT IN MYOTONIC-DYSTROPHY, AMERICAN JOURNAL OF HUMAN GENETICS 54: 414 (1994).

2. BRUNNER, H.G., INFLUENCE OF SEX OF THE TRANSMITTING PARENT AS WELL AS OF PARENTAL ALLELE SIZE ON THE CTG EXPANSION IN MYOTONIC-DYSTROPHY (DM), AMERICAN JOURNAL OF HUMAN GENETICS 53: 1016 (1993).

3. CALLEN, D.F., HIGH-RESOLUTION CYTOGENETIC-BASED PHYSICAL MAP OF HUMAN CHROMOSOME-16, GENOMICS 13: 1178 (1992).

4. DUYAO, M, TRINUCLEOTIDE REPEAT LENGTH INSTABILITY AND AGE-OF-ONSET IN HUNTINGTONS-DISEASE, NATURE GENETICS 4: 387 (1993).

5. FU, Y.H., VARIATION OF THE CGG REPEAT AT THE FRAGILE-X SITE RESULTS IN GENETIC INSTABILITY - RESOLUTION OF THE SHERMAN PARADOX, CELL 67: 1047 (1991).

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