Genetic Hearing Impairment: Its Clinical Presentations (Advances in Oto-Rhino-Laryngology, Vol. 61)
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Genetic Hearing Impairment : Its Clinical Presentations
~EN HC USISBN: 9783805574495 bzw. 3805574495, vermutlich in Englisch, Karger AG, S. gebundenes Buch, gebraucht.
Von Händler/Antiquariat, ThriftBooks [54239181], AURORA, IL, U.S.A.
An apparently unread copy in perfect condition. Dust cover is intact; pages are clean and are not marred by notes or folds of any kind. At ThriftBooks, our motto is: Read More, Spend Less.
An apparently unread copy in perfect condition. Dust cover is intact; pages are clean and are not marred by notes or folds of any kind. At ThriftBooks, our motto is: Read More, Spend Less.
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Genetic Hearing Impairment: Its Clinical Presentations
DEISBN: 9783805574495 bzw. 3805574495, in Deutsch, S. Karger AG (Switzerland).
Lieferung aus: Vereinigte Staaten von Amerika, Lagernd.
Genetic Hearing Impairment: Its Clinical Presentations Agel-Pahlke, Cornelia W. R. J. / Cremers, C. W. R. J. Presenting the phenotype of genetic non-syndromic and the most frequent syndromic types of hearing impairment A decade of innovative findings in the research of molecular biology of hearing and deafness is reflected in this volume. The genetic causes for many types of syndromic and non-syndromic deafness are identified and genotypic-phenotypic relationships are explored. Although the type and degree of deafness caused by mutations in different genes significantly overlap, relatively unique age-related audiometric profiles are also emerging. For example, the audioprofile of DFNA1 and DFNA6-14 is a low-frequency sensorineural hearing loss; with DFNA8-14 it is a mid-frequency sensorineural hearing loss, and with DFNA2, DFNA5 and DFNA20-26 it is a high-frequency progressive hearing loss. Recognizing such audioprofiles can facilitate well-guided decision-making in clinical practice and can direct genetic testing for deafness. With an accurate genetic diagnosis, prognostic information can be provided to patients and their families. In the future, gene-specific habilitation options may also become available. To keep up to date with new clinical standards of diagnosing genetic hearing impairment, this book is indispensable reading to otorhinolaryngologists and audiologists.
Genetic Hearing Impairment: Its Clinical Presentations Agel-Pahlke, Cornelia W. R. J. / Cremers, C. W. R. J. Presenting the phenotype of genetic non-syndromic and the most frequent syndromic types of hearing impairment A decade of innovative findings in the research of molecular biology of hearing and deafness is reflected in this volume. The genetic causes for many types of syndromic and non-syndromic deafness are identified and genotypic-phenotypic relationships are explored. Although the type and degree of deafness caused by mutations in different genes significantly overlap, relatively unique age-related audiometric profiles are also emerging. For example, the audioprofile of DFNA1 and DFNA6-14 is a low-frequency sensorineural hearing loss; with DFNA8-14 it is a mid-frequency sensorineural hearing loss, and with DFNA2, DFNA5 and DFNA20-26 it is a high-frequency progressive hearing loss. Recognizing such audioprofiles can facilitate well-guided decision-making in clinical practice and can direct genetic testing for deafness. With an accurate genetic diagnosis, prognostic information can be provided to patients and their families. In the future, gene-specific habilitation options may also become available. To keep up to date with new clinical standards of diagnosing genetic hearing impairment, this book is indispensable reading to otorhinolaryngologists and audiologists.
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Genetic Hearing Impairment: Its Clinical Presentations (Advances in Oto-Rhino-Laryngology, Vol. 61) (2002)
DE US FEISBN: 9783805574495 bzw. 3805574495, Band: 61, in Deutsch, S. Karger, gebraucht, Erstausgabe.
Von Händler/Antiquariat, Better World Books [51315977], Mishawaka, IN, U.S.A.
Former Library book. Shows some signs of wear, and may have some markings on the inside.
Former Library book. Shows some signs of wear, and may have some markings on the inside.
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Genetic Hearing Impairment: Its Clinical Presentations (Advances in Oto-Rhino-Laryngology, Vol. 61)
DE HC NWISBN: 9783805574495 bzw. 3805574495, Band: 61, in Deutsch, S. Karger, gebundenes Buch, neu.
Von Händler/Antiquariat, Cloud 9 Books [52294834], Wellington, FL, U.S.A.
3805574495 New Condition.
3805574495 New Condition.
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Genetic Hearing Impairment: Its Clinical Presentations. Advances in Oto-Rhino-Laryngology, Vol. 61. (2002)
EN HC USISBN: 9783805574495 bzw. 3805574495, Band: 61, in Englisch, 248 Seiten, Karger, S, gebundenes Buch, gebraucht.
Lieferung aus: Deutschland, Versandfertig in 1 - 2 Werktagen, Versandkostenfrei. Tatsächliche Versandkosten können abweichen.
Von Händler/Antiquariat, betterworldbooks__.
Gebundene Ausgabe, Label: Karger, S, Karger, S, Produktgruppe: Book, Publiziert: 2002-09, Studio: Karger, S.
Von Händler/Antiquariat, betterworldbooks__.
Gebundene Ausgabe, Label: Karger, S, Karger, S, Produktgruppe: Book, Publiziert: 2002-09, Studio: Karger, S.
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Genetic Hearing Impairment: Its Clinical Presentations. Advances in Oto-Rhino-Laryngology, Vol. 61. (2002)
EN HC NWISBN: 9783805574495 bzw. 3805574495, Band: 61, in Englisch, 248 Seiten, Karger, S, gebundenes Buch, neu.
Lieferung aus: Deutschland, Versandfertig in 1 - 2 Werktagen, Versandkostenfrei. Tatsächliche Versandkosten können abweichen.
Von Händler/Antiquariat, Wadie Shop " We Deliver in 4 Working days "
Gebundene Ausgabe, Label: Karger, S, Karger, S, Produktgruppe: Book, Publiziert: 2002-09, Studio: Karger, S.
Von Händler/Antiquariat, Wadie Shop " We Deliver in 4 Working days "
Gebundene Ausgabe, Label: Karger, S, Karger, S, Produktgruppe: Book, Publiziert: 2002-09, Studio: Karger, S.
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