Crossref Citations
This article has been cited by the following publications. This list is generated based on data provided by Crossref.
Searle, A. G.
Ford, C. E.
and
Beechey, C. V.
1971.
Meiotic disjunction in mouse translocations and the determination of centromere position.
Genetical Research,
Vol. 18,
Issue. 2,
p.
215.
Robinson, Roy
1972.
Gene Mapping in Laboratory Mammals Part B.
p.
151.
Lim, David J.
and
Erway, Lawrence C.
1974.
Influence of Manganese on Genetically Defective Otolith.
Annals of Otology, Rhinology & Laryngology,
Vol. 83,
Issue. 5,
p.
565.
DEOL, M. S.
1975.
Racial differences in pigmentation and natural selection.
Annals of Human Genetics,
Vol. 38,
Issue. 4,
p.
501.
Kalter, H.
1980.
A compendium of the genetically induced congenital Malformations of the mouse.
Teratology,
Vol. 21,
Issue. 3,
p.
397.
GREEN, EARL L.
1981.
Methods of Animal Experimentation.
p.
1.
Gibb, S.
Håkansson, E. M.
Lundin, L.-G.
and
Shire, J. G. M.
1981.
Reduced pigmentation (rp), a new coat colour gene with effects on kidney lysosomal glycosidases in the mouse.
Genetical Research,
Vol. 37,
Issue. 1,
p.
95.
Trune, Dennis R.
and
Lim, David J.
1983.
A morphometric study of the pallid mutant mouse inner ear.
American Journal of Otolaryngology,
Vol. 4,
Issue. 4,
p.
261.
DEOL, M.S.
1983.
Development of Auditory and Vestibular Systems.
p.
309.
Trune, Dennis R.
and
Lim, David J.
1983.
The Behavior and Vestibular Nuclear Morphology of Otoconia-Deficient Pallid Mutant Mice.
Journal of Neurogenetics,
Vol. 1,
Issue. 1,
p.
53.
Wilson, Doris Burda
1985.
Issues and Reviews in Teratology.
p.
239.
Drabkin, H.
Sage, M.
Helms, C.
Green, P.
Gemmill, R.
Smith, D.
Erickson, P.
Hart, I.
Ferguson-Smith, A.
Ruddle, F.
and
Tommerup, N.
1989.
Regional and physical mapping studies characterizing the Greig polysyndactyly 3;7 chromosome translocation, t(3;7)(p21.1;p13).
Genomics,
Vol. 4,
Issue. 4,
p.
518.
Justice, Monica J.
Silan, Colleen M.
Ceci, Jeffrey D.
Buchberg, Arthur M.
Copeland, Neal G.
and
Jenkins, Nancy A.
1990.
A molecular genetic linkage map of mouse chromosome 13 anchored by the beige (bg) and satin (sa) loci.
Genomics,
Vol. 6,
Issue. 2,
p.
341.
Asher, J H
and
Friedman, T B
1990.
Mouse and hamster mutants as models for Waardenburg syndromes in humans..
Journal of Medical Genetics,
Vol. 27,
Issue. 10,
p.
618.
Cattanach, Bruce
Peters, Jo
and
Searle, Tony
1990.
Mary Lyon: An Appreciation.
Genetics Research,
Vol. 56,
Issue. 2-3,
p.
83.
Justice, Monica J.
and
Stephenson, Dennis A.
1991.
Mouse chromosome 13.
Mammalian Genome,
Vol. 1,
Issue. S1,
p.
S205.
Justice, Monica J.
and
Stephenson, Dennis A.
1992.
Mouse Chromosome 13.
Mammalian Genome,
Vol. 3,
Issue. S1,
p.
S195.
Masuya, H
Sagai, T
Wakana, S
Moriwaki, K
and
Shiroishi, T
1995.
A duplicated zone of polarizing activity in polydactylous mouse mutants..
Genes & Development,
Vol. 9,
Issue. 13,
p.
1645.
O'Brien, E. P.
Novak, E. K.
Zhen, L.
Manly, K. F.
Stephenson, D.
and
Swank, R. T.
1995.
Molecular markers near two mouse Chromosome 13 genes, muted and pearl, which cause platelet storage pool deficiency (SPD).
Mammalian Genome,
Vol. 6,
Issue. 1,
p.
19.
Kingsmore, S. F.
Barbosa, M. D. F. S.
Nguyen, Q. A.
Ashley, J. A.
Blaydes, S. M.
Tchernev, V. T.
Detter, J. C.
and
Lovett, M.
1996.
Physical mapping of the beige critical region on mouse Chromosome 13.
Mammalian Genome,
Vol. 7,
Issue. 10,
p.
773.