Results
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61.
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62.
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Restriction fragment polymorphisms of the HLA-DR, HLA-DQ, and insulin gene regions in IDDM: the GAW5 data. [electronic resource] by
- Cox, N J
- Gogolin, K J
- Horvath, V J
- Barker, D F
- Wright, E
- Tran, T
- Skolnick, M H
- Boehm, B O
- Fehsel, K
- Bertrams, J
Producer: 19890725
In:
Genetic epidemiology vol. 6
Availability: No items available.
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63.
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Identification of new markers in Xp21 between DXS28 (C7) and DMD. [electronic resource] by
- Worley, K C
- Towbin, J A
- Zhu, X M
- Barker, D F
- Ballabio, A
- Chamberlain, J
- Biesecker, L G
- Blethen, S L
- Brosnan, P
- Fox, J E
Producer: 19920922
In:
Genomics vol. 13
Availability: No items available.
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64.
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Consortium fine localization of X-linked Charcot-Marie-Tooth disease (CMTX1): additional support that connexin32 is the defect in CMTX1. [electronic resource] by
- Pericak-Vance, M A
- Barker, D F
- Bergoffen, J A
- Chance, P
- Cochrane, S
- Dahl, N
- Exler, M C
- Fain, P R
- Fairweather, N D
- Fischbeck, K
Producer: 19950824
In:
Human heredity vol. 45
Availability: No items available.
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65.
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Identification of mutations in the COL4A5 collagen gene in Alport syndrome. [electronic resource] by
- Barker, D F
- Hostikka, S L
- Zhou, J
- Chow, L T
- Oliphant, A R
- Gerken, S C
- Gregory, M C
- Skolnick, M H
- Atkin, C L
- Tryggvason, K
Producer: 19900711
In:
Science (New York, N.Y.) vol. 248
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66.
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The duplication in Charcot-Marie-Tooth disease type 1a spans at least 1100 kb on chromosome 17p11.2. [electronic resource] by
- Hoogendijk, J E
- Hensels, G W
- Zorn, I
- Valentijn, L
- Janssen, E A
- de Visser, M
- Barker, D F
- Ongerboer de Visser, B W
- Baas, F
- Bolhuis, P A
Producer: 19920204
In:
Human genetics vol. 88
Availability: No items available.
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67.
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High-density genetic and physical mapping of DNA markers near the X-linked Alport syndrome locus: definition and use of flanking polymorphic markers. [electronic resource] by
- Barker, D F
- Fain, P R
- Goldgar, D E
- Dietz-Band, J N
- Turco, A E
- Kashtan, C E
- Gregory, M C
- Tryggvason, K
- Skolnick, M H
- Atkin, C L
Producer: 19920204
In:
Human genetics vol. 88
Availability: No items available.
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68.
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Chromosome 17 deletions and p53 gene mutations in colorectal carcinomas. [electronic resource] by
- Baker, S J
- Fearon, E R
- Nigro, J M
- Hamilton, S R
- Preisinger, A C
- Jessup, J M
- vanTuinen, P
- Ledbetter, D H
- Barker, D F
- Nakamura, Y
- White, R
- Vogelstein, B
Producer: 19890512
In:
Science (New York, N.Y.) vol. 244
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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Expression of mRNA for type IV collagen alpha1, alpha5 and alpha6 chains by cultured dermal fibroblasts from patients with X-linked Alport syndrome. [electronic resource] by
- Sasaki, S
- Zhou, B
- Fan, W W
- Kim, Y
- Barker, D F
- Denison, J C
- Atkin, C L
- Gregory, M C
- Zhou, J
- Segal, Y
- Sado, Y
- Ninomiya, Y
- Michael, A F
- Kashtan, C E
Producer: 19981124
In:
Matrix biology : journal of the International Society for Matrix Biology vol. 17
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71.
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Nonmuscle myosin heavy chain IIA mutations define a spectrum of autosomal dominant macrothrombocytopenias: May-Hegglin anomaly and Fechtner, Sebastian, Epstein, and Alport-like syndromes. [electronic resource] by
- Heath, K E
- Campos-Barros, A
- Toren, A
- Rozenfeld-Granot, G
- Carlsson, L E
- Savige, J
- Denison, J C
- Gregory, M C
- White, J G
- Barker, D F
- Greinacher, A
- Epstein, C J
- Glucksman, M J
- Martignetti, J A
Producer: 20011207
In:
American journal of human genetics vol. 69
Availability: No items available.
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