Crossref Citations
This article has been cited by the following publications. This list is generated based on data provided by Crossref.
Lyon, Mary F.
1963.
Attempts to test the inactive-X theory of dosage compensation in mammals.
Genetical Research,
Vol. 4,
Issue. 1,
p.
93.
Russell, Liane B.
1964.
SECTION OF BIOLOGICAL AND MEDICAL SCIENCES: ANOTHER LOOK AT THE SINGLE‐ACTIVE‐X HYPOTHESIS*.
Transactions of the New York Academy of Sciences,
Vol. 26,
Issue. 6 Series II,
p.
726.
Mukherjee, Barid B.
1965.
CYTOLOGICAL ASPECT OF THE X-CHROMOSOME DIFFERENTIATION IN NORMAL AND ABNORMAL CELLS.
Canadian Journal of Genetics and Cytology,
Vol. 7,
Issue. 2,
p.
189.
Grüneberg, Hans
1966.
The case for somatic crossing over in the mouse.
Genetical Research,
Vol. 7,
Issue. 1,
p.
58.
Grüneberg, Hans
1966.
More about the. tabby mouse and about the Lyon hypothesis.
Development,
Vol. 16,
Issue. 3,
p.
569.
Ohno, Susumu
1966.
Sex Chromosomes and Sex-linked Genes.
Vol. 1 ,
Issue. ,
p.
101.
Lyon, Mary F.
1966.
Order of loci on the X-chromosome of the mouse.
Genetical Research,
Vol. 7,
Issue. 1,
p.
130.
Ohno, Susumu
1966.
Sex Chromosomes and Sex-Linked Genes.
Vol. 1,
Issue. ,
p.
101.
Grüneberg, Hans
1969.
Threshold phenomena versus cell heredity in the manifestation of sex-linked genes in mammals.
Development,
Vol. 22,
Issue. 2,
p.
145.
Robinson, Roy
1972.
Gene Mapping in Laboratory Mammals Part B.
p.
151.
Robinson, Roy
1972.
Gene Mapping in Laboratory Mammals.
p.
151.
Phillips, Rita J. S.
Hawker, S. G.
and
Moseley, H. J.
1973.
Bare-patches, a new sex-linked gene in the mouse, associated with a high production of XO females: I. A preliminary report of breeding experiments.
Genetical Research,
Vol. 22,
Issue. 1,
p.
91.
Guenet, Jean-Louis
1979.
A sex-linked coat-colour mutation in the mouse non-transmissible through the female.
Genetical Research,
Vol. 33,
Issue. 2,
p.
163.
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.
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.
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.
Nwokoro, Ngozi A.
Wassif, Christopher A.
and
Porter, Forbes D.
2001.
Genetic Disorders of Cholesterol Biosynthesis in Mice and Humans.
Molecular Genetics and Metabolism,
Vol. 74,
Issue. 1-2,
p.
105.
Kelley, Richard I.
and
Herman, Gail E.
2001.
INBORNERRORS OFSTEROLBIOSYNTHESIS.
Annual Review of Genomics and Human Genetics,
Vol. 2,
Issue. 1,
p.
299.
Nakamura, M.
Sundberg, J. P.
and
Paus, R.
2001.
Mutant laboratory mice with abnormalities in hair follicle morphogenesis, cycling, and/or structure: annotated tables.
Experimental Dermatology,
Vol. 10,
Issue. 6,
p.
369.