Somatic Segregation, Recombination, Asymmetrical Distribution and Complementation Tests of Cytoplasmically-Inherited Antibiotic-Resistance Mitochondrial Markers in S. CEREVISIAE

Por Rank, G. H., Bech-Hansen, N. T.
Publicado em 1972

Manifestations of X-linked congenital stationary night blindness in three daughters of an affected male: demonstration of homozygosity.

Por Bech-Hansen, N T, Pearce, W G
Publicado em 1993

Duplication of the human immunoglobulin heavy chain gamma 2 gene.

Por Bech-Hansen, N T, Cox, D W
Publicado em 1986

SacI RFLP recognized by a human immunoglobulin kappa light chain constant region probe.

Por Field, L L, Tobias, R, Bech-Hansen, T
Publicado em 1987

TaqI RFLP in human adenylate kinase-1 (AK1) gene region on chromosome 9.

Por Bech-Hansen, N T, Marshall, K J, Kraus, S L
Publicado em 1989

A polymorphic dinucleotide repeat at the DXS7 locus

Por Moore, B.J., Kwan, S.-P., Bech-Hansen, N.T.
Publicado em 1992

Human TaqI RFLP recognized by neurofilament gene probes.

Por Bech-Hansen, N T, Marshall, K J, Kraus, S L
Publicado em 1988

Restriction fragment length polymorphisms associated with immunoglobulin C gamma genes reveal linkage disequilibrium and genomic organization.

Por Bech-Hansen, N T, Linsley, P S, Cox, D W
Publicado em 1983

A multigene deletion within the immunoglobulin heavy-chain region.

Por Chaabani, H, Bech-Hansen, N T, Cox, D W
Publicado em 1985

Channeling Vision: Ca(V)1.4—A Critical Link in Retinal Signal Transmission

Por Waldner, D. M., Bech-Hansen, N. T., Stell, W. K.
Publicado no Biomed Res Int (2018)

Analysis of a break in chromosome 14 mapping to the region of the immunoglobulin heavy chain locus.

Por Linsley, P S, Bech-Hansen, N T, Siminovitch, L, Cox, D W
Publicado em 1983

Der(22)t(11;22) resulting from a paternal de novo translocation, adjacent 1 segregation, and maternal heterodisomy of chromosome 22.

Por Dawson, A J, Mears, A J, Chudley, A E, Bech-Hansen, T, McDermid, H
Publicado em 1996

X linked cone‐rod dystrophy, CORDX3, is caused by a mutation in the CACNA1F gene

Por Jalkanen, R, Mäntyjärvi, M, Tobias, R, Isosomppi, J, Sankila, E‐M, Alitalo, T, Bech‐Hansen, N T
Publicado em 2006

A new genetic locus for X linked progressive cone-rod dystrophy

Por Jalkanen, R, Demirci, F, Tyynismaa, H, Bech-Hansen, T, Meindl, A, Peippo, M, Mantyjarvi, M, Gorin, M, Alitalo, T
Publicado em 2003

Transcriptional activity of the human tissue inhibitor of metalloproteinases 1 (TIMP-1) gene in fibroblasts involves elements in the promoter, exon 1 and intron 1.

Por Clark, I M, Rowan, A D, Edwards, D R, Bech-Hansen, T, Mann, D A, Bahr, M J, Cawston, T E
Publicado em 1997

Cone dystrophy and ectopic synaptogenesis in a Cacna1f loss of function model of congenital stationary night blindness (CSNB2A)

Por Waldner, D. M., Giraldo Sierra, N. C., Bonfield, S., Nguyen, L., Dimopoulos, I. S., Sauvé, Y., Stell, W. K., Bech-Hansen, N. T.
Publicado no Channels (Austin) (2018)

Recent Progress in the Identification of the X-Linked Infantile Spinal Muscular Atrophy (Xl-SMA) Gene: Implications for Neuronal Apoptosis

Por Baumbach, L. L., Dressman, D., Basterrechea, H., Ahearn, M. E., Bech-Hansen, N. T., Clark, R. D., Meind, A., Hoffman, E.
Publicado no ScientificWorldJournal (2001)

Clinical Characteristics, Mutation Spectrum, and Prevalence of Åland Eye Disease/Incomplete Congenital Stationary Night Blindness in Denmark

Por Hove, Marianne N., Kilic-Biyik, Kevser Z., Trotter, Alana, Grønskov, Karen, Sander, Birgit, Larsen, Michael, Carroll, Joseph, Bech-Hansen, Torben, Rosenberg, Thomas
Publicado no Invest Ophthalmol Vis Sci (2016)

Evidence for genetic heterogeneity in X-linked congenital stationary night blindness.

Por Boycott, K M, Pearce, W G, Musarella, M A, Weleber, R G, Maybaum, T A, Birch, D G, Miyake, Y, Young, R S, Bech-Hansen, N T
Publicado em 1998

ROHHAD and Prader-Willi syndrome (PWS): clinical and genetic comparison

Por Barclay, Sarah F., Rand, Casey M., Nguyen, Lisa, Wilson, Richard J. A., Wevrick, Rachel, Gibson, William T., Bech-Hansen, N. Torben, Weese-Mayer, Debra E.
Publicado no Orphanet J Rare Dis (2018)