Results
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121.
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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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122.
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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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123.
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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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124.
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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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125.
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Human and rabbit paraoxonases: purification, cloning, sequencing, mapping and role of polymorphism in organophosphate detoxification. [electronic resource] by
- Furlong, C E
- Costa, L G
- Hassett, C
- Richter, R J
- Sundstrom, J A
- Adler, D A
- Disteche, C M
- Omiecinski, C J
- Chapline, C
- Crabb, J W
Producer: 19930903
In:
Chemico-biological interactions vol. 87
Availability: No items available.
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126.
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Human huntingtin derived from YAC transgenes compensates for loss of murine huntingtin by rescue of the embryonic lethal phenotype. [electronic resource] by
- Hodgson, J G
- Smith, D J
- McCutcheon, K
- Koide, H B
- Nishiyama, K
- Dinulos, M B
- Stevens, M E
- Bissada, N
- Nasir, J
- Kanazawa, I
- Disteche, C M
- Rubin, E M
- Hayden, M R
Producer: 19970314
In:
Human molecular genetics vol. 5
Availability: No items available.
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127.
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Cloning and characterization of rat density-enhanced phosphatase-1, a protein tyrosine phosphatase expressed by vascular cells. [electronic resource] by
- Borges, L G
- Seifert, R A
- Grant, F J
- Hart, C E
- Disteche, C M
- Edelhoff, S
- Solca, F F
- Lieberman, M A
- Lindner, V
- Fischer, E H
- Lok, S
- Bowen-Pope, D F
Producer: 19961024
In:
Circulation research vol. 79
Availability: No items available.
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128.
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cDNA cloning and chromosome mapping of the human Fe65 gene: interaction of the conserved cytoplasmic domains of the human beta-amyloid precursor protein and its homologues with the mouse Fe65 protein. [electronic resource] by
- Bressler, S L
- Gray, M D
- Sopher, B L
- Hu, Q
- Hearn, M G
- Pham, D G
- Dinulos, M B
- Fukuchi, K
- Sisodia, S S
- Miller, M A
- Disteche, C M
- Martin, G M
Producer: 19970204
In:
Human molecular genetics vol. 5
Availability: No items available.
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129.
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Recurrent duplication and deletion polymorphisms on the long arm of the Y chromosome in normal males. [electronic resource] by
- Jobling, M A
- Samara, V
- Pandya, A
- Fretwell, N
- Bernasconi, B
- Mitchell, R J
- Gerelsaikhan, T
- Dashnyam, B
- Sajantila, A
- Salo, P J
- Nakahori, Y
- Disteche, C M
- Thangaraj, K
- Singh, L
- Crawford, M H
- Tyler-Smith, C
Producer: 19970311
In:
Human molecular genetics vol. 5
Availability: No items available.
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130.
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The mouse Mid1 gene: implications for the pathogenesis of Opitz syndrome and the evolution of the mammalian pseudoautosomal region. [electronic resource] by
- Dal Zotto, L
- Quaderi, N A
- Elliott, R
- Lingerfelter, P A
- Carrel, L
- Valsecchi, V
- Montini, E
- Yen, C H
- Chapman, V
- Kalcheva, I
- Arrigo, G
- Zuffardi, O
- Thomas, S
- Willard, H F
- Ballabio, A
- Disteche, C M
- Rugarli, E I
Producer: 19980416
In:
Human molecular genetics vol. 7
Availability: No items available.
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131.
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Rare trisomy mosaicism diagnosed in amniocytes, involving an autosome other than chromosomes 13, 18, 20, and 21: karyotype/phenotype correlations. [electronic resource] by
- Hsu, L Y
- Yu, M T
- Neu, R L
- Van Dyke, D L
- Benn, P A
- Bradshaw, C L
- Shaffer, L G
- Higgins, R R
- Khodr, G S
- Morton, C C
- Wang, H
- Brothman, A R
- Chadwick, D
- Disteche, C M
- Jenkins, L S
- Kalousek, D K
- Pantzar, T J
- Wyatt, P
Producer: 19970722
In:
Prenatal diagnosis vol. 17
Availability: No items available.
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