Results
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141.
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142.
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Evidence against DNA polymerase beta as a candidate gene for Werner syndrome. [electronic resource] by
- Chang, M
- Burmer, G C
- Sweasy, J
- Loeb, L A
- Edelhoff, S
- Disteche, C M
- Yu, C E
- Anderson, L
- Oshima, J
- Nakura, J
Producer: 19940602
In:
Human genetics vol. 93
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143.
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144.
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146.
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147.
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148.
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149.
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150.
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151.
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Integrated mapping analysis of the Werner syndrome region of chromosome 8. [electronic resource] by
- Oshima, J
- Yu, C E
- Boehnke, M
- Weber, J L
- Edelhoff, S
- Wagner, M J
- Wells, D E
- Wood, S
- Disteche, C M
- Martin, G M
Producer: 19950217
In:
Genomics vol. 23
Availability: No items available.
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152.
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Orientation-dependent Dxz4 contacts shape the 3D structure of the inactive X chromosome. [electronic resource] by
- Bonora, G
- Deng, X
- Fang, H
- Ramani, V
- Qiu, R
- Berletch, J B
- Filippova, G N
- Duan, Z
- Shendure, J
- Noble, W S
- Disteche, C M
Producer: 20181217
In:
Nature communications vol. 9
Availability: No items available.
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153.
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Evidence of evolutionary up-regulation of the single active X chromosome in mammals based on Clc4 expression levels in Mus spretus and Mus musculus. [electronic resource] by
- Adler, D A
- Rugarli, E I
- Lingenfelter, P A
- Tsuchiya, K
- Poslinski, D
- Liggitt, H D
- Chapman, V M
- Elliott, R W
- Ballabio, A
- Disteche, C M
Producer: 19970917
In:
Proceedings of the National Academy of Sciences of the United States of America vol. 94
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154.
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Minor Xp21 chromosome deletion in a male associated with expression of Duchenne muscular dystrophy, chronic granulomatous disease, retinitis pigmentosa, and McLeod syndrome. [electronic resource] by
- Francke, U
- Ochs, H D
- de Martinville, B
- Giacalone, J
- Lindgren, V
- Distèche, C
- Pagon, R A
- Hofker, M H
- van Ommen, G J
- Pearson, P L
Producer: 19850513
In:
American journal of human genetics vol. 37
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155.
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The human acid ceramidase gene (ASAH): structure, chromosomal location, mutation analysis, and expression. [electronic resource] by
- Li, C M
- Park, J H
- He, X
- Levy, B
- Chen, F
- Arai, K
- Adler, D A
- Disteche, C M
- Koch, J
- Sandhoff, K
- Schuchman, E H
Producer: 20000209
In:
Genomics vol. 62
Availability: No items available.
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156.
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Cloning and primary structure of a human islet isoform of glutamic acid decarboxylase from chromosome 10. [electronic resource] by
- Karlsen, A E
- Hagopian, W A
- Grubin, C E
- Dube, S
- Disteche, C M
- Adler, D A
- Bärmeier, H
- Mathewes, S
- Grant, F J
- Foster, D
- Lernmark, Åke
Producer: 19911031
In:
Proceedings of the National Academy of Sciences of the United States of America vol. 88
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157.
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A candidate gene for the amnionless gastrulation stage mouse mutation encodes a TRAF-related protein. [electronic resource] by
- Wang, X
- Bornslaeger, E A
- Haub, O
- Tomihara-Newberger, C
- Lonberg, N
- Dinulos, M B
- Disteche, C M
- Copeland, N
- Gilbert, D J
- Jenkins, N A
- Lacy, E
Producer: 19960827
In:
Developmental biology vol. 177
Availability: No items available.
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158.
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DNA deletion associated with hereditary neuropathy with liability to pressure palsies. [electronic resource] by
- Chance, P F
- Alderson, M K
- Leppig, K A
- Lensch, M W
- Matsunami, N
- Smith, B
- Swanson, P D
- Odelberg, S J
- Disteche, C M
- Bird, T D
Producer: 19930224
In:
Cell vol. 72
Availability: No items available.
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159.
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The DAZ gene cluster on the human Y chromosome arose from an autosomal gene that was transposed, repeatedly amplified and pruned. [electronic resource] by
- Saxena, R
- Brown, L G
- Hawkins, T
- Alagappan, R K
- Skaletsky, H
- Reeve, M P
- Reijo, R
- Rozen, S
- Dinulos, M B
- Disteche, C M
- Page, D C
Producer: 19961216
In:
Nature genetics vol. 14
Availability: No items available.
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160.
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CD40 ligand gene defects responsible for X-linked hyper-IgM syndrome. [electronic resource] by
- Allen, R C
- Armitage, R J
- Conley, M E
- Rosenblatt, H
- Jenkins, N A
- Copeland, N G
- Bedell, M A
- Edelhoff, S
- Disteche, C M
- Simoneaux, D K
Producer: 19930322
In:
Science (New York, N.Y.) vol. 259
Availability: No items available.
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