Crossref Citations
This article has been cited by the following publications. This list is generated based on data provided by
Crossref.
Phillips, Rita J. S.
and
Kaufman, M. H.
1974.
Bare-patches, a new sex-linked gene in the mouse, associated with a high production ofXOfemales: II. Investigations into the nature and mechanism of theXOproduction.
Genetical Research,
Vol. 24,
Issue. 1,
p.
27.
1974.
Review Lecture: Mechanisms and evolutionary origins of variable X-chromosome activity in mammals.
Proceedings of the Royal Society of London. Series B. Biological Sciences,
Vol. 187,
Issue. 1088,
p.
243.
EVANS, E. P.
and
PHILLIPS, RITA J. S.
1975.
Inversion heterozygosity and the origin of XO daughters of Bpa/+ female mice.
Nature,
Vol. 256,
Issue. 5512,
p.
40.
Russell, Liane Brauch
1976.
Chemical Mutagens.
p.
55.
Happle, R.
1979.
X-Linked dominant chondrodysplasia punctata.
Human Genetics,
Vol. 53,
Issue. 1,
p.
65.
Happle, R.
Phillips, R. J. S.
Roessner, A.
and
Jünemann, G.
1983.
Homologous genes for X-linked chondrodysplasia punctata in man and mouse.
Human Genetics,
Vol. 63,
Issue. 1,
p.
24.
Speed, R. M.
1986.
Oocyte development in XO foetuses of man and mouse: the possible role of heterologous X-chromosome pairing in germ cell survival.
Chromosoma,
Vol. 94,
Issue. 2,
p.
115.
Davisson, Muriel T.
1987.
X-Linked genetic homologies between mouse and man.
Genomics,
Vol. 1,
Issue. 3,
p.
213.
Traupe, Heiko
1989.
The Ichthyoses.
p.
179.
Herman, Gail E.
and
Walton, Sandy J.
1990.
Close linkage of the murine locus bare patches to the X-linked visual pigment gene: Implications for mapping human X-linked dominant chondrodysplasia punctata.
Genomics,
Vol. 7,
Issue. 3,
p.
307.
Herman, Gail E.
Faust, Cynthia J.
Darlison, Mark G.
and
Barnard, Eric A.
1991.
Genetic mapping of the mouse X chromosome in the region homologous to human Xq27–Xq28.
Genomics,
Vol. 9,
Issue. 4,
p.
670.
Chatterjee, Aurobindo
Faust, Cynthia J.
and
Herman, Gail E.
1993.
Genetic and physical mapping of the biglycan gene on the mouse X Chromosome.
Mammalian Genome,
Vol. 4,
Issue. 1,
p.
33.
Angel, Tiffany A.
Faust, Cynthia J.
Gonzales, Juanita C.
Kenwrick, Susan
Lewis, Richard Alan
and
Herman, Gail E.
1993.
Genetic mapping of the X-linked dominant mutations striated (Str) and bare patches (Bpa) to a 600-kb region of the mouse X Chromosome: implications for mapping human disorders in Xq28.
Mammalian Genome,
Vol. 4,
Issue. 3,
p.
171.
Levin, M L
Chatterjee, A
Pragliola, A
Worley, K C
Wehnert, M
Zhuchenko, O
Smith, R F
Lee, C C
and
Herman, G E
1996.
A comparative transcription map of the murine bare patches (Bpa) and striated (Str) critical regions and human Xq28..
Genome Research,
Vol. 6,
Issue. 6,
p.
465.
Sundberg, John P.
and
King, Lloyd E.
1996.
Mouse Mutations as Animal Models and Biomedical Tools for Dermatological Research.
Journal of Investigative Dermatology,
Vol. 106,
Issue. 2,
p.
368.
Mevorah, Barukh
and
Politi, Yael
1997.
Genodermatoses in women.
Clinics in Dermatology,
Vol. 15,
Issue. 1,
p.
17.
Liu, Xiao Yu
Dangel, Andrew W.
Kelley, Richard I.
Zhao, Wei
Denny, Paul
Botcherby, Marc
Cattanach, Bruce
Peters, Jo
Hunsicker, Patricia R.
Mallon, Ann-Marie
Strivens, Mark A.
Bate, Rachael
Miller, Webb
Rhodes, Michael
Brown, Stephen D.M.
and
Herman, Gail E.
1999.
The gene mutated in bare patches and striated mice encodes a novel 3β-hydroxysteroid dehydrogenase.
Nature Genetics,
Vol. 22,
Issue. 2,
p.
182.
K�nig, Arne
Happle, Rudolf
Bornholdt, Dorothea
Engel, Hartmut
and
Grzeschik, Karl-Heinz
2000.
Mutations in the NSDHL gene, encoding a 3?-hydroxysteroid dehydrogenase, cause CHILD syndrome.
American Journal of Medical Genetics,
Vol. 90,
Issue. 4,
p.
339.
Moebius, Fabian F.
Fitzky, Barbara U.
and
Glossmann, Hartmut
2000.
Genetic Defects in Postsqualene Cholesterol Biosynthesis.
Trends in Endocrinology & Metabolism,
Vol. 11,
Issue. 3,
p.
106.
Kelley, Richard I.
and
Herman, Gail E.
2001.
INBORNERRORS OFSTEROLBIOSYNTHESIS.
Annual Review of Genomics and Human Genetics,
Vol. 2,
Issue. 1,
p.
299.