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De Kok YJM, van der Maarel SM, Bitner-Glindzicz M, Huber I, et al. (1995) Asso-
ciation between X-linked mixed deafness and mutations in the POU domain gene
POU3F4 . Science 267:685-689.
Deloukas P, Schuler GD, Gyapay G, Beasley EM, et al. (1998) A physical map of
30,000 human genes. Science 282:744-746.
Dib C, Faure S, Fizames C, Samson D, et al. (1996) A comprehensive genetic map
of the human genome based on 5,264 microsatellites. Nature 380:152-154.
Dietrich W, Copeland N, Gilbert D, Miller J, Jenkins N, Lander E (1995) Mapping
the mouse genome: Current status and future prospects. Proc Natl Acad Sci, USA
92:10849-10853.
Duyk G, Kim S, Myers R, Cox D (1990) Exon trapping: a genetic screen to identify
candidate transcribed sequences in cloned mammalian genomic DNA. Proc Natl
Acad Sci, USA 87:8995-8999.
Ellis TP, Humphrey KE, Smith MJ, Cotton RG (1998) Chemical cleavage of mis-
match: A new look at an established method. Hum Mutat 11:345-353.
Everett L, Glaser B, Beck J, Idol J, et al. (1997) Pendred syndrome is caused by
mutations in a putative sulphate transporter gene ( PDS ).
Nature Genet
17:411- 422.
Faerman A, Shani M (1997) Transgenic mice: production and analysis of expression.
Methods Cell Biol 52:373-403.
Fischer S, Lerman L (1979) Length-independent separation of DNA restriction frag-
ments in two-dimensional gel-electrophoresis. Cell 16:191-200.
Foy C, Newton V, Wellesley D, Harris R, Read A (1990) Assignment of WS I locus
to 2q37 and possible homology between Waardenburg syndrome and the Splotch
mouse. Am J Hum Genet 46:1017-1023.
Friedman R, Ryan A (1992) Transgenic mice. Current applications to the study of
the auditory and vestibular systems. Otolaryngology Clin North America 25:
1017-1026.
Friedman R (1996) Transgenic insertional mutagenesis. Applications to inner-ear
genetics. Arch Otolaryngol Head Neck Surg 122:252-257.
Frohman M, Dush M, Martin G (1988) Rapid production of full-length cDNAs from
rare transcripts; amplification using a single gene-specific oligonucleotide primer.
Proc Natl Acad Sci, USA 85:8998-9002.
Guilford P, Arab SB, Blanchard S, Levilliers J, et al. (1994) A non-syndromic form
of neurosensory, recessive deafness maps to the pericentromeric region of chro-
mosome 13q. Nature Genet 6:24-28.
Gyapay G, Morissette J, Vignal A, Dib C, et al. (1994) Généthon human genetic
linkage map. Nature Genet 7:246-339.
Ishikirikyama S, Tonoki H, Shibuya Y, Chin S, et al. (1989) Waardenburg syndrome
type I in a child with de novo inversion (2) (q35q37.3). Am J Med Genet
33:505-507.
Juyal R, Figuera L, Hauge X, Elsea S, et al. (1996) Molecular analyses of 17p11.2
deletions in 62 Smith-Magenis syndrome patients. Am J Hum Genet 58:998-1007.
Kashtan C, Fish A, Kieppel M, Yoshioka K, Michael A (1986) Nephritogenic antigen
determinant in epidermal and renal basement membranes of kindreds with
Alport-type familial nephritis. J Clin Inv 78:1035-1044.
Kelley P, Harris D, Comer B, Askew J, et al. (1998) Novel mutations in the connexin
26 (GJB2) that cause autosomal recessive (DFNB1) hearing loss. American
Journal of Human Genetics 62:792-799.
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