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Mitochondrial Inheritance of Acquired Deafness.
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- Annals of the New York Academy of Sciences, 1991, v. 630, n. 1, p. 301, doi. 10.1111/j.1749-6632.1991.tb19613.x
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Malformation and Degeneration Inner Ear of MOS Transgenic Mice<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1991, v. 630, n. 1, p. 268, doi. 10.1111/j.1749-6632.1991.tb19601.x
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Transforming Growth Factor-Beta.
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- Annals of the New York Academy of Sciences, 1991, v. 630, n. 1, p. 253, doi. 10.1111/j.1749-6632.1991.tb19596.x
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Ascertainment of Families with Hereditary Deafness for Linkage Studies.
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- Annals of the New York Academy of Sciences, 1991, v. 630, n. 1, p. 293, doi. 10.1111/j.1749-6632.1991.tb19610.x
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Localization of a Gene for Waardenburg Syndrome Type I<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1991, v. 630, n. 1, p. 143, doi. 10.1111/j.1749-6632.1991.tb19583.x
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International Symposium on the Genetics of Hearing Impairment Introduction.
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- Annals of the New York Academy of Sciences, 1991, v. 630, n. 1, p. 1, doi. 10.1111/j.1749-6632.1991.tb19569.x
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Genetic Epidemiology of Hearing Impairment.
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- Annals of the New York Academy of Sciences, 1991, v. 630, n. 1, p. 16, doi. 10.1111/j.1749-6632.1991.tb19572.x
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Human Genetic Mapping and Inherited Deafness Syndromes.
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- Annals of the New York Academy of Sciences, 1991, v. 630, n. 1, p. 38, doi. 10.1111/j.1749-6632.1991.tb19574.x
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Comparative Gene Mapping, Genome Duplication, and the Genetics of Hearing<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1991, v. 630, n. 1, p. 49, doi. 10.1111/j.1749-6632.1991.tb19575.x
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Molecular Genetics of X-Linked Hearing Impairment.
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- Annals of the New York Academy of Sciences, 1991, v. 630, n. 1, p. 176, doi. 10.1111/j.1749-6632.1991.tb19586.x
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Neurofibromatosis 2 (Bilateral Acoustic or Central Neurofibromatosis), a Treatable Cause of Deafness.
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- Annals of the New York Academy of Sciences, 1991, v. 630, n. 1, p. 305, doi. 10.1111/j.1749-6632.1991.tb19615.x
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Gene Expression in Narmal and Abnormal Inner Ears<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1991, v. 630, n. 1, p. 129, doi. 10.1111/j.1749-6632.1991.tb19581.x
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Reverse Genetics in the Mouse and Its Application to the Study of Deafness<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1991, v. 630, n. 1, p. 80, doi. 10.1111/j.1749-6632.1991.tb19577.x
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Sociological Implications of Hearing Loss.
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- Annals of the New York Academy of Sciences, 1991, v. 630, n. 1, p. 230, doi. 10.1111/j.1749-6632.1991.tb19592.x
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Neurosensory Relationships in the Cochlea of the Bronx Waltzer Mouse<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1991, v. 630, n. 1, p. 270, doi. 10.1111/j.1749-6632.1991.tb19602.x
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Hearing Loss Etiolgy in a group of 996 Children.
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- Annals of the New York Academy of Sciences, 1991, v. 630, n. 1, p. 315, doi. 10.1111/j.1749-6632.1991.tb19619.x
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Anomalies of the Auditory Organ in Chromosomal Syndromes.
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- Annals of the New York Academy of Sciences, 1991, v. 630, n. 1, p. 281, doi. 10.1111/j.1749-6632.1991.tb19605.x
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Genetic Counseling of the Deaf<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1991, v. 630, n. 1, p. 212, doi. 10.1111/j.1749-6632.1991.tb19590.x
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National Deaf Register as a Resource for Hereditary Deafness Research.
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- Annals of the New York Academy of Sciences, 1991, v. 630, n. 1, p. 292, doi. 10.1111/j.1749-6632.1991.tb19609.x
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Approaches to Genetic Counseling.
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- Annals of the New York Academy of Sciences, 1991, v. 630, n. 1, p. 223, doi. 10.1111/j.1749-6632.1991.tb19591.x
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Genetics of Hearing Impairment Welcome-an Overview.
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- Annals of the New York Academy of Sciences, 1991, v. 630, n. 1, p. 3, doi. 10.1111/j.1749-6632.1991.tb19570.x
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Congenital Hypothyroidism<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1991, v. 630, n. 1, p. 274, doi. 10.1111/j.1749-6632.1991.tb19603.x
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Initiation of Chondrogenesis in Cultured Periotic Mesenchyme.
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- Annals of the New York Academy of Sciences, 1991, v. 630, n. 1, p. 256, doi. 10.1111/j.1749-6632.1991.tb19597.x
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The Genetic Anatomy of Hearing.
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- Annals of the New York Academy of Sciences, 1991, v. 630, n. 1, p. 32, doi. 10.1111/j.1749-6632.1991.tb19573.x
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An Evaluation of Otopathology in the MOV-13 Transgenic Mutant Mouse<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1991, v. 630, n. 1, p. 249, doi. 10.1111/j.1749-6632.1991.tb19595.x
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Assessment of Families from the Deaf Community.
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- Annals of the New York Academy of Sciences, 1991, v. 630, n. 1, p. 308, doi. 10.1111/j.1749-6632.1991.tb19616.x
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Acquired Causes of Deafness in Childhood.
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- Annals of the New York Academy of Sciences, 1991, v. 630, n. 1, p. 197, doi. 10.1111/j.1749-6632.1991.tb19588.x
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Otosderosis<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1991, v. 630, n. 1, p. 319, doi. 10.1111/j.1749-6632.1991.tb19621.x
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Audiologic Investigation of Autosomal Dominant Hereditary Sensory Hearing Loss in a Family of 507 Members in 6 Generations.
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- Annals of the New York Academy of Sciences, 1991, v. 630, n. 1, p. 310, doi. 10.1111/j.1749-6632.1991.tb19617.x
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Clinical and Genetic Aspects in Autosomal Dominant Inherited Osteogenesis Imperfecta Type I.
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- Annals of the New York Academy of Sciences, 1991, v. 630, n. 1, p. 240, doi. 10.1111/j.1749-6632.1991.tb19594.x
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HLA Antigen Frequencies in Sensorineural Hearing Impairment of Suspected Genetic Origin.
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- Annals of the New York Academy of Sciences, 1991, v. 630, n. 1, p. 303, doi. 10.1111/j.1749-6632.1991.tb19614.x
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The Molecular and Structural Basis of Hearing Impairment in Mice with the cpk Mutant Gene.
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- Annals of the New York Academy of Sciences, 1991, v. 630, n. 1, p. 262, doi. 10.1111/j.1749-6632.1991.tb19599.x
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Hearing Impairment and Pigmentary Disturbance<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1991, v. 630, n. 1, p. 152, doi. 10.1111/j.1749-6632.1991.tb19584.x
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Confirmation of the Location of a Waardenburg Syndrome Type I Mutation on Human Chromosome 2q<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1991, v. 630, n. 1, p. 295, doi. 10.1111/j.1749-6632.1991.tb19611.x
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Genetic Studies of Usher Syndrome.
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- Annals of the New York Academy of Sciences, 1991, v. 630, n. 1, p. 167, doi. 10.1111/j.1749-6632.1991.tb19585.x
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The History of the Genetics of Hearing Impairment<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1991, v. 630, n. 1, p. 6, doi. 10.1111/j.1749-6632.1991.tb19571.x
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Hearing Impairment in Mice with the cmd/cmd (Cartilage Matrix Deficiency) Mutant Gene.
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- Annals of the New York Academy of Sciences, 1991, v. 630, n. 1, p. 265, doi. 10.1111/j.1749-6632.1991.tb19600.x
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A Progress Report on the Localization of Usher Syndrome Type II to Chromosome 1q<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1991, v. 630, n. 1, p. 284, doi. 10.1111/j.1749-6632.1991.tb19606.x
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Tissue Interactions and Growth Factors that Control Development of the Inner Ear.
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- Annals of the New York Academy of Sciences, 1991, v. 630, n. 1, p. 116, doi. 10.1111/j.1749-6632.1991.tb19580.x
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A Basic Prerequisite for the Understanding of Hereditary Deafness at the Genome Level.
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- Annals of the New York Academy of Sciences, 1991, v. 630, n. 1, p. 277, doi. 10.1111/j.1749-6632.1991.tb19604.x
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The Search for Branchiootorenal Syndrome on Chromosomes 1 and 8.
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- Annals of the New York Academy of Sciences, 1991, v. 630, n. 1, p. 288, doi. 10.1111/j.1749-6632.1991.tb19607.x
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Ultrastructural Changes of Cochlea in Mice with Hereditary Chondrodysplasia (cho/cho).
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- Annals of the New York Academy of Sciences, 1991, v. 630, n. 1, p. 259, doi. 10.1111/j.1749-6632.1991.tb19598.x
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Recurrence Risks.
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- Annals of the New York Academy of Sciences, 1991, v. 630, n. 1, p. 203, doi. 10.1111/j.1749-6632.1991.tb19589.x
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Reverse Genetic Approaches to Cloning Deafness Genes<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1991, v. 630, n. 1, p. 93, doi. 10.1111/j.1749-6632.1991.tb19578.x
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Similarities between -Mice and Humans with Hereditary Deafness.
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- Annals of the New York Academy of Sciences, 1991, v. 630, n. 1, p. 68, doi. 10.1111/j.1749-6632.1991.tb19576.x
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Audiologic Profile in Niemann-Pick C.
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- Annals of the New York Academy of Sciences, 1991, v. 630, n. 1, p. 313, doi. 10.1111/j.1749-6632.1991.tb19618.x
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Profound Childhood Deafness in Southern Africa.
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- Annals of the New York Academy of Sciences, 1991, v. 630, n. 1, p. 290, doi. 10.1111/j.1749-6632.1991.tb19608.x
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A Model Program for Genetic Counseling of the Deaf<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1991, v. 630, n. 1, p. 317, doi. 10.1111/j.1749-6632.1991.tb19620.x
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Genetic Analysis of Complex Disorders.
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- Annals of the New York Academy of Sciences, 1991, v. 630, n. 1, p. 100, doi. 10.1111/j.1749-6632.1991.tb19579.x
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Nonsyndromal Profound Genetic Deafness in Childhood.
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- Annals of the New York Academy of Sciences, 1991, v. 630, n. 1, p. 191, doi. 10.1111/j.1749-6632.1991.tb19587.x
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