Results
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61.
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Large multi-chromosomal duplications encompass many members of the olfactory receptor gene family in the human genome. [electronic resource] by
- Trask, B J
- Massa, H
- Brand-Arpon, V
- Chan, K
- Friedman, C
- Nguyen, O T
- Eichler, E
- van den Engh, G
- Rouquier, S
- Shizuya, H
- Giorgi, D
Producer: 19990121
In:
Human molecular genetics vol. 7
Availability: No items available.
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62.
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Molecular characterization of a patient with del(1)(q23-q25). [electronic resource] by
- Franco, B
- Lai, L W
- Patterson, D
- Ledbetter, D H
- Trask, B J
- van den Engh, G
- Iannaccone, S
- Frances, S
- Patel, P I
- Lupski, J R
Producer: 19910912
In:
Human genetics vol. 87
Availability: No items available.
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63.
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Isolation and characterization of the cDNA encoding human DNA methyltransferase. [electronic resource] by
- Yen, R W
- Vertino, P M
- Nelkin, B D
- Yu, J J
- el-Deiry, W
- Cumaraswamy, A
- Lennon, G G
- Trask, B J
- Celano, P
- Baylin, S B
Producer: 19920630
In:
Nucleic acids research vol. 20
Availability: No items available.
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64.
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Somatic cell hybrids, sequence-tagged sites, simple repeat polymorphisms, and yeast artificial chromosomes for physical and genetic mapping of proximal 17p. [electronic resource] by
- Guzzetta, V
- Franco, B
- Trask, B J
- Zhang, H
- Saucedo-Cardenas, O
- Montes de Oca-Luna, R
- Greenberg, F
- Chinault, A C
- Lupski, J R
- Patel, P I
Producer: 19920828
In:
Genomics vol. 13
Availability: No items available.
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65.
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Smith-Magenis syndrome deletion: a case with equivocal cytogenetic findings resolved by fluorescence in situ hybridization. [electronic resource] by
- Juyal, R C
- Greenberg, F
- Mengden, G A
- Lupski, J R
- Trask, B J
- van den Engh, G
- Lindsay, E A
- Christy, H
- Chen, K S
- Baldini, A
Producer: 19960130
In:
American journal of medical genetics vol. 58
Availability: No items available.
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66.
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Evolution of the mammalian G protein alpha subunit multigene family. [electronic resource] by
- Wilkie, T M
- Gilbert, D J
- Olsen, A S
- Chen, X N
- Amatruda, T T
- Korenberg, J R
- Trask, B J
- de Jong, P
- Reed, R R
- Simon, M I
Producer: 19930610
In:
Nature genetics vol. 1
Availability: No items available.
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67.
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Evidence for a recessive PMP22 point mutation in Charcot-Marie-Tooth disease type 1A. [electronic resource] by
- Roa, B B
- Garcia, C A
- Pentao, L
- Killian, J M
- Trask, B J
- Suter, U
- Snipes, G J
- Ortiz-Lopez, R
- Shooter, E M
- Patel, P I
- Lupski, J R
Producer: 19940113
In:
Nature genetics vol. 5
Availability: No items available.
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68.
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The gene for the peripheral myelin protein PMP-22 is a candidate for Charcot-Marie-Tooth disease type 1A. [electronic resource] by
- Patel, P I
- Roa, B B
- Welcher, A A
- Schoener-Scott, R
- Trask, B J
- Pentao, L
- Snipes, G J
- Garcia, C A
- Francke, U
- Shooter, E M
- Lupski, J R
- Suter, U
Producer: 19930623
In:
Nature genetics vol. 1
Availability: No items available.
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69.
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DNA duplication associated with Charcot-Marie-Tooth disease type 1A. [electronic resource] by
- Lupski, J R
- de Oca-Luna, R M
- Slaugenhaupt, S
- Pentao, L
- Guzzetta, V
- Trask, B J
- Saucedo-Cardenas, O
- Barker, D F
- Killian, J M
- Garcia, C A
- Chakravarti, A
- Patel, P I
Producer: 19910827
In:
Cell vol. 66
Availability: No items available.
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70.
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Quantification by flow cytometry of chromosome-17 deletions in Smith-Magenis syndrome patients. [electronic resource] by
- Trask, B J
- Mefford, H
- van den Engh, G
- Massa, H F
- Juyal, R C
- Potocki, L
- Finucane, B
- Abuelo, D N
- Witt, D R
- Magenis, E
- Baldini, A
- Greenberg, F
- Lupski, J R
- Patel, P I
Producer: 19970106
In:
Human genetics vol. 98
Availability: No items available.
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71.
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Mutations in the BRCA1-associated RING domain (BARD1) gene in primary breast, ovarian and uterine cancers. [electronic resource] by
- Thai, T H
- Du, F
- Tsan, J T
- Jin, Y
- Phung, A
- Spillman, M A
- Massa, H F
- Muller, C Y
- Ashfaq, R
- Mathis, J M
- Miller, D S
- Trask, B J
- Baer, R
- Bowcock, A M
Producer: 19980317
In:
Human molecular genetics vol. 7
Availability: No items available.
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72.
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Androgen receptor YAC transgenic mice carrying CAG 45 alleles show trinucleotide repeat instability. [electronic resource] by
- La Spada, A R
- Peterson, K R
- Meadows, S A
- McClain, M E
- Jeng, G
- Chmelar, R S
- Haugen, H A
- Chen, K
- Singer, M J
- Moore, D
- Trask, B J
- Fischbeck, K H
- Clegg, C H
- McKnight, G S
Producer: 19980619
In:
Human molecular genetics vol. 7
Availability: No items available.
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73.
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Alagille syndrome is caused by mutations in human Jagged1, which encodes a ligand for Notch1. [electronic resource] by
- Li, L
- Krantz, I D
- Deng, Y
- Genin, A
- Banta, A B
- Collins, C C
- Qi, M
- Trask, B J
- Kuo, W L
- Cochran, J
- Costa, T
- Pierpont, M E
- Rand, E B
- Piccoli, D A
- Hood, L
- Spinner, N B
Producer: 19970729
In:
Nature genetics vol. 16
Availability: No items available.
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74.
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Members of the olfactory receptor gene family are contained in large blocks of DNA duplicated polymorphically near the ends of human chromosomes. [electronic resource] by
- Trask, B J
- Friedman, C
- Martin-Gallardo, A
- Rowen, L
- Akinbami, C
- Blankenship, J
- Collins, C
- Giorgi, D
- Iadonato, S
- Johnson, F
- Kuo, W L
- Massa, H
- Morrish, T
- Naylor, S
- Nguyen, O T
- Rouquier, S
- Smith, T
- Wong, D J
- Youngblom, J
- van den Engh, G
Producer: 19980226
In:
Human molecular genetics vol. 7
Availability: No items available.
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75.
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A high-resolution radiation hybrid map of the human genome draft sequence. [electronic resource] by
- Olivier, M
- Aggarwal, A
- Allen, J
- Almendras, A A
- Bajorek, E S
- Beasley, E M
- Brady, S D
- Bushard, J M
- Bustos, V I
- Chu, A
- Chung, T R
- De Witte, A
- Denys, M E
- Dominguez, R
- Fang, N Y
- Foster, B D
- Freudenberg, R W
- Hadley, D
- Hamilton, L R
- Jeffrey, T J
- Kelly, L
- Lazzeroni, L
- Levy, M R
- Lewis, S C
- Liu, X
- Lopez, F J
- Louie, B
- Marquis, J P
- Martinez, R A
- Matsuura, M K
- Misherghi, N S
- Norton, J A
- Olshen, A
- Perkins, S M
- Perou, A J
- Piercy, C
- Piercy, M
- Qin, F
- Reif, T
- Sheppard, K
- Shokoohi, V
- Smick, G A
- Sun, W L
- Stewart, E A
- Fernando, J
- Tran, N M
- Trejo, T
- Vo, N T
- Yan, S C
- Zierten, D L
- Zhao, S
- Sachidanandam, R
- Trask, B J
- Myers, R M
- Cox, D R
Producer: 20010315
In:
Science (New York, N.Y.) vol. 291
Availability: No items available.
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76.
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Integration of cytogenetic landmarks into the draft sequence of the human genome. [electronic resource] by
- Cheung, V G
- Nowak, N
- Jang, W
- Kirsch, I R
- Zhao, S
- Chen, X N
- Furey, T S
- Kim, U J
- Kuo, W L
- Olivier, M
- Conroy, J
- Kasprzyk, A
- Massa, H
- Yonescu, R
- Sait, S
- Thoreen, C
- Snijders, A
- Lemyre, E
- Bailey, J A
- Bruzel, A
- Burrill, W D
- Clegg, S M
- Collins, S
- Dhami, P
- Friedman, C
- Han, C S
- Herrick, S
- Lee, J
- Ligon, A H
- Lowry, S
- Morley, M
- Narasimhan, S
- Osoegawa, K
- Peng, Z
- Plajzer-Frick, I
- Quade, B J
- Scott, D
- Sirotkin, K
- Thorpe, A A
- Gray, J W
- Hudson, J
- Pinkel, D
- Ried, T
- Rowen, L
- Shen-Ong, G L
- Strausberg, R L
- Birney, E
- Callen, D F
- Cheng, J F
- Cox, D R
- Doggett, N A
- Carter, N P
- Eichler, E E
- Haussler, D
- Korenberg, J R
- Morton, C C
- Albertson, D
- Schuler, G
- de Jong, P J
- Trask, B J
Producer: 20010322
In:
Nature vol. 409
Availability: No items available.
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