Biology Reference
In-Depth Information
Ishikiriyama S, Tonoki H, Shibuya Y, Chin S, et al. (1989) Waardenburg syn-
drome type I in a child with a de novo inversion 2(q35-q37.3). Am J Med Genet
33:505.
Jervelle A, Lange-Nielsen F (1957) Congenital deaf mutism, functional heart disease
with prolongation of the QT interval and sudden death. Am Heart J 54:59-
68.
Kelsell DP, Dunlop J, Stevens HP, Lench NJ, et al. (1999) Connexin 26 mutations in
hereditary non-syndromic sensorineural deafness. Nature 387:80-83.
Konigsmark BB, Gorlin RJ (1976) Genetic and Metabolic Deafness. Philadelphia:
WB Saunders, pp. 1-419.
Kraatz JJ (1925) Hereditary deaf-mutism: A study of the Mendelian factors in the
inheritance of deaf-mutism. J Hered 16:265-270.
Kruglyak L, Lander ES (1995) High resolution genetic mapping of complex traits.
Am J Hum Genet 56:1212-1223.
Lai CS, Fisher SE, Hurst, JA, Varga-Khadem F, Monaco AP (2001) A forkhead-
domain gene is mutated in a severe speech and language disorder. Nature
413:519-523.
Lander ES, Botstein D (1987) Homozygosity mapping: A way to map human reces-
sive traits with the DNA of inbred children. Science 236:1567-1570.
Lathrop GM, Lalouel JM, Juliet C, Ott J (1984) Strategies for multilocus linkage
analysis in humans. Proc Nat Acad Sci 81:3443.
Lerer I, Sagi M, Ben-Neriah Z, Wang T, Levi H, Abeliovich D (2001) A deletion
mutation in GJB6 cooperating with a GJB2 mutation in trans in non-syndromic
deafness: A novel founder mutation in Ashkenazi jews. Human Mutation, muta-
tion in brief #458, online, http://www.mutationresearch.com/mutat/show/
Liu XZ, Walsh J, Tamagawa Y, Kitamura K, et al. (1977a) Autosomal dominant non-
syndromic deafness (DFNA11) caused by a mutation in the myosin VIIA gene.
Nature Genet 17:268.
Liu XZ, Walsh J, Mburu P, Kendrick-Jones J, et al. (1977b) Mutations in the myosin
VIIA gene cause non-syndromic recessive deafness.
Nature Genet 16:188-
190.
Liu XZ, Xu LR, Zhang SL, Xu Y (1994) Epidemiological and genetic studies of con-
genital profound deafness. Am J Med Genet 53:192-195.
Macklin MT, Mann HB, Whitney R (1946) Studies on the inheritance of deafness
in the pupils of the Clarke School for the Deaf: (b) The genetic analysis of the
pedigree data of the Clarke School pupils. Laryngoscope 56:583-601.
Marazita ML, Ploughman LM, Rawlings B, Remington E, et al. (1993) Genetic
epidemiologic studies of early-onset deafness in the U.S. school-age population.
Am J Med Genet 46:486.
Middleton A, Hewison J, Mueller RF (1998) Attitudes of deaf adults towards genetic
testing for hereditary deafness. Am J Hum Genet 63:1175-1180.
Morell R, Spritz RA, Ho L, Pierpont J, et al. (1997) Apparent digenic inheritance
of Waardenburg syndrome type 2 (WS2) and autosomal recessive ocular albinism
(AROA). Hum Mol Genet 6:659-664.
Mori T (1957) On the inheritance of sporadic deaf-mutism. Jap J Genet 32:252; as
cited in Chung, et al. (1959).
Morton NE (1991) Genetic epidemiology of hearing loss. Ann NY Acad Sci
630:16-31.
Mygind H (1894) Deaf-mutism. London: FJ Rebman.
Search WWH ::




Custom Search