Mapping of the otogelin gene (OTGN) to mouse Chromosome 7 and human Chromosome 11p14.3: a candidate for human autosomal recessive nonsyndromic deafness DFNB18

1999 ◽  
Vol 10 (5) ◽  
pp. 520-522 ◽  
Author(s):  
Martine Cohen-Salmon ◽  
Marie-Geneviève Mattei ◽  
Christine Petit
Keyword(s):  
Human Chromosome ◽  
Mouse Chromosome ◽  
Autosomal Recessive ◽  
Chromosome 7 ◽  
Nonsyndromic Deafness

Mapping of theARIXHomeodomain Gene to Mouse Chromosome 7 and Human Chromosome 11q13

Genomics ◽  
1996 ◽  
Vol 33 (3) ◽  
pp. 527-531 ◽  
Author(s):  
Kenneth R. Johnson ◽  
Leslie Smith ◽  
Dabney K. Johnson ◽  
Jennifer Rhodes ◽  
Eugene M. Rinchik ◽  
...  
Keyword(s):  
Human Chromosome ◽  
Mouse Chromosome ◽  
Chromosome 7 ◽  
Chromosome 11Q13

scholarly journals The Epimorphin Gene Is Highly Conserved among Humans, Mice, and Rats and Maps to Human Chromosome 7, Mouse Chromosome 5, and Rat Chromosome 12

Genomics ◽  
1996 ◽  
Vol 37 (3) ◽  
pp. 386-389 ◽  
Author(s):  
Hongbin Zha ◽  
Elaine F. Remmers ◽  
Claude Szpirer ◽  
Josiane Szpirer ◽  
Heying Zhang ◽  
...  
Keyword(s):  
Human Chromosome ◽  
Mouse Chromosome ◽  
Chromosome 7 ◽  
Chromosome 12 ◽  
Chromosome 5 ◽  
Human Chromosome 7

Assignment of the gene (RLBP1) for cellular retinaldehyde-binding protein (CRALBP) to human chromosome 15q26 and mouse chromosome 7

Genomics ◽  
1992 ◽  
Vol 12 (1) ◽  
pp. 58-62 ◽  
Author(s):  
Robert S. Sparkes ◽  
Camilla Heinzmann ◽  
Steve Goldflam ◽  
Tracy Kojis ◽  
John C. Saari ◽  
...  
Keyword(s):  
Human Chromosome ◽  
Mouse Chromosome ◽  
Binding Protein ◽  
Chromosome 7

scholarly journals Genetic and cytogenetic localisation of the homeo box containing genes on mouse chromosome 6 and human chromosome 7.

1986 ◽  
Vol 5 (11) ◽  
pp. 2899-2905 ◽  
Author(s):  
M. Bućan ◽  
T. Yang-Feng ◽  
A.M. Colberg-Poley ◽  
D.J. Wolgemuth ◽  
J.L. Guenet ◽  
...  
Keyword(s):  
Human Chromosome ◽  
Mouse Chromosome ◽  
Chromosome 7 ◽  
Chromosome 6 ◽  
Homeo Box ◽  
Cytogenetic Localisation ◽  
Human Chromosome 7

Establishment of the mouse chromosome 7 region with homology to the myotonic dystrophy region of human chromosome 19q

Genomics ◽  
1990 ◽  
Vol 7 (1) ◽  
pp. 12-18 ◽  
Author(s):  
J.S. Cavanna ◽  
A.J. Greenfield ◽  
K.J. Johnson ◽  
A.R. Marks ◽  
B. Nadal-Ginard ◽  
...  
Keyword(s):  
Human Chromosome ◽  
Myotonic Dystrophy ◽  
Mouse Chromosome ◽  
Chromosome 7 ◽  
Chromosome 19Q
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