Results
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81.
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82.
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Mutations in transcript isoforms of the neurofibromatosis 2 gene in multiple human tumour types. [electronic resource] by
- Bianchi, A B
- Hara, T
- Ramesh, V
- Gao, J
- Klein-Szanto, A J
- Morin, F
- Menon, A G
- Trofatter, J A
- Gusella, J F
- Seizinger, B R
Producer: 19940525
In:
Nature genetics vol. 6
Availability: No items available.
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83.
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p53 mutations are associated with 17p allelic loss in grade II and grade III astrocytoma. [electronic resource] by
- von Deimling, A
- Eibl, R H
- Ohgaki, H
- Louis, D N
- von Ammon, K
- Petersen, I
- Kleihues, P
- Chung, R Y
- Wiestler, O D
- Seizinger, B R
Producer: 19920612
In:
Cancer research vol. 52
Availability: No items available.
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84.
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Frequent NF2 gene transcript mutations in sporadic meningiomas and vestibular schwannomas. [electronic resource] by
- Lekanne Deprez, R H
- Bianchi, A B
- Groen, N A
- Seizinger, B R
- Hagemeijer, A
- van Drunen, E
- Bootsma, D
- Koper, J W
- Avezaat, C J
- Kley, N
Producer: 19940630
In:
American journal of human genetics vol. 54
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85.
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Clinical and genetic studies of renal cell carcinomas in a family with a constitutional chromosome 3;8 translocation. Genetics of familial renal carcinoma. [electronic resource] by
- Li, F P
- Decker, H J
- Zbar, B
- Stanton, V P
- Kovacs, G
- Seizinger, B R
- Aburatani, H
- Sandberg, A A
- Berg, S
- Hosoe, S
- Brown, R S
Producer: 19930113
In:
Annals of internal medicine vol. 118
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86.
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Genetic linkage analysis of neurofibromatosis with DNA markers. [electronic resource] by
- Seizinger, B R
- Tanzi, R E
- Gilliam, T C
- Bader, J L
- Parry, D M
- Spence, M A
- Marazita, M L
- Gibbons, K
- Hobbs, W
- Gusella, J F
Producer: 19870501
In:
Annals of the New York Academy of Sciences vol. 486
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87.
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Von Hippel-Lindau disease maps to the region of chromosome 3 associated with renal cell carcinoma. [electronic resource] by
- Seizinger, B R
- Rouleau, G A
- Ozelius, L J
- Lane, A H
- Farmer, G E
- Lamiell, J M
- Haines, J
- Yuen, J W
- Collins, D
- Majoor-Krakauer, D
Producer: 19880420
In:
Nature vol. 332
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88.
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Genetic flanking markers refine diagnostic criteria and provide insights into the genetics of Von Hippel Lindau disease. [electronic resource] by
- Seizinger, B R
- Smith, D I
- Filling-Katz, M R
- Neumann, H
- Green, J S
- Choyke, P L
- Anderson, K M
- Freiman, R N
- Klauck, S M
- Whaley, J
Producer: 19910506
In:
Proceedings of the National Academy of Sciences of the United States of America vol. 88
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89.
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Flanking markers for the gene causing von Recklinghausen neurofibromatosis (NF1). [electronic resource] by
- Seizinger, B R
- Farmer, G E
- Haines, J L
- Ozelius, L J
- Anderson, K
- Korf, B R
- Parry, D M
- Pericak-Vance, M A
- Mulvihill, J J
- Menon, A
Producer: 19890123
In:
American journal of human genetics vol. 44
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90.
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Characterization of a translocation within the von Recklinghausen neurofibromatosis region of chromosome 17. [electronic resource] by
- Menon, A G
- Ledbetter, D H
- Rich, D C
- Seizinger, B R
- Rouleau, G A
- Michels, V F
- Schmidt, M A
- Dewald, G
- DallaTorre, C M
- Haines, J L
Producer: 19891109
In:
Genomics vol. 5
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91.
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Genetic linkage of bilateral acoustic neurofibromatosis to a DNA marker on chromosome 22. [electronic resource] by
- Rouleau, G A
- Wertelecki, W
- Haines, J L
- Hobbs, W J
- Trofatter, J A
- Seizinger, B R
- Martuza, R L
- Superneau, D W
- Conneally, P M
- Gusella, J F
Producer: 19871019
In:
Nature vol. 329
Availability: No items available.
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92.
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Comparative study of p53 gene and protein alterations in human astrocytic tumors. [electronic resource] by
- Louis, D N
- von Deimling, A
- Chung, R Y
- Rubio, M P
- Whaley, J M
- Eibl, R H
- Ohgaki, H
- Wiestler, O D
- Thor, A D
- Seizinger, B R
Producer: 19930302
In:
Journal of neuropathology and experimental neurology vol. 52
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93.
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Central nervous system involvement in Von Hippel-Lindau disease. [electronic resource] by
- Filling-Katz, M R
- Choyke, P L
- Oldfield, E
- Charnas, L
- Patronas, N J
- Glenn, G M
- Gorin, M B
- Morgan, J K
- Linehan, W M
- Seizinger, B R
Producer: 19910207
In:
Neurology vol. 41
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94.
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Genetic linkage of von Recklinghausen neurofibromatosis to the nerve growth factor receptor gene. [electronic resource] by
- Seizinger, B R
- Rouleau, G A
- Ozelius, L J
- Lane, A H
- Faryniarz, A G
- Chao, M V
- Huson, S
- Korf, B R
- Parry, D M
- Pericak-Vance, M A
Producer: 19870709
In:
Cell vol. 49
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95.
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Physical mapping of a translocation breakpoint in neurofibromatosis. [electronic resource] by
- Fountain, J W
- Wallace, M R
- Bruce, M A
- Seizinger, B R
- Menon, A G
- Gusella, J F
- Michels, V V
- Schmidt, M A
- Dewald, G W
- Collins, F S
Producer: 19890713
In:
Science (New York, N.Y.) vol. 244
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96.
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A kindred with a variant of multiple endocrine neoplasia type 1 demonstrating frequent expression of pituitary tumors but not linked to the multiple endocrine neoplasia type 1 locus at chromosome region 11q13. [electronic resource] by
- Stock, J L
- Warth, M R
- Teh, B T
- Coderre, J A
- Overdorf, J H
- Baumann, G
- Hintz, R L
- Hartman, M L
- Seizinger, B R
- Larsson, C
- Aronin, N
Producer: 19970311
In:
The Journal of clinical endocrinology and metabolism vol. 82
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97.
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Linkage analysis in von Recklinghausen neurofibromatosis (NF1) with DNA markers for chromosome 17. [electronic resource] by
- Seizinger, B R
- Rouleau, G A
- Lane, A H
- Farmer, G
- Ozelius, L J
- Haines, J L
- Parry, D M
- Korf, B R
- Pericak-Vance, M A
- Faryniarz, A G
Producer: 19880616
In:
Genomics vol. 1
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98.
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Development of highly potent inhibitors of Ras farnesyltransferase possessing cellular and in vivo activity. [electronic resource] by
- Leftheris, K
- Kline, T
- Vite, G D
- Cho, Y H
- Bhide, R S
- Patel, D V
- Patel, M M
- Schmidt, R J
- Weller, H N
- Andahazy, M L
- Carboni, J M
- Gullo-Brown, J L
- Lee, F Y
- Ricca, C
- Rose, W C
- Yan, N
- Barbacid, M
- Hunt, J T
- Meyers, C A
- Seizinger, B R
- Zahler, R
- Manne, V
Producer: 19960301
In:
Journal of medicinal chemistry vol. 39
Availability: No items available.
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