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001 ocn851697583
003 OCoLC
005 20200110051046.3
006 m o d
007 cr cnu---unuuu
008 130705s2013 enk ob 001 0 eng d
010 2012049476
019 857427726|a1129367731
020 9780199313884|q(electronic book)
020 0199313881|q(electronic book)
020 1299708889|q(electronic book)
020 9781299708884|q(electronic book)
020 |z9780199731961|q(hardback ;|qalkaline paper)
020 |z0199731969|q(hardback ;|qalkaline paper)
035 (OCoLC)851697583|z(OCoLC)857427726|z(OCoLC)1129367731
037 502139|bMIL
040 IDEBK|beng|epn|cIDEBK|dN$T|dEBLCP|dYDXCP|dMHW|dE7B|dOHS
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049 RIDW
050 4 RF292|b.H474 2013eb
072 7 HEA|x035000|2bisacsh
072 7 MED|x007000|2bisacsh
082 04 617.8/0642|223
090 RF292|b.H474 2013eb
245 00 Hereditary hearing loss and its syndromes /|cedited by
Helga V. Toriello, Shelley D. Smith.
250 3rd ed.
264 1 Oxford :|bOxford University Press,|c[2013]
264 4 |c©2013
300 1 online resource.
336 text|btxt|2rdacontent
337 computer|bc|2rdamedia
338 online resource|bcr|2rdacarrier
340 |gpolychrome|2rdacc
347 text file|2rdaft
490 1 Oxford monographs on medical genetics ;|v63
504 Includes bibliographical references and index.
505 0 Genetic hearing loss : a brief history -- Epidemiology,
etiology, genetic mechanisms, and genetic counseling --
Embryology of the mammalian ear -- Gene/environment
interactions in acquired hearing loss -- Syndrome
diagnosis and investigation in the hearing-impaired
patient -- Genetic hearing loss with no associated
abnormities -- Genetic hearing loss associated with
external ear abnormalities -- Eye disorders -- Genetic
hearing loss associated with musculoskeletal disorders --
Genetic hearing loss associated with renal disorders --
Genetic hearing loss associated with neurologic and
neuromuscular disorders -- Genetics hearing loss
associated with cardiac abnormalities -- Genetic hearing
loss associated with endocrine disorders -- Genetic
hearing loss associated with metabolic disorders --
Integumentary disorders -- Oral and dental disorderss --
Chromosome disorders.
520 This is the third edition of the foremost medical
reference on hereditary hearing loss. Chapters on
epidemiology, embryology, non-syndromic hearing loss, and
syndromic forms of hearing loss have all been updated with
particular attention to the vast amount of new information
on molecular mechanisms, and chapters on clinical and
molecular diagnosis and on genetic susceptibility to
ototoxic factors have been added.
588 0 Print version record.
590 eBooks on EBSCOhost|bEBSCO eBook Subscription Academic
Collection - North America
650 0 Deafness|xGenetic aspects.|0https://id.loc.gov/authorities
/subjects/sh85036069
650 0 Hearing disorders|0https://id.loc.gov/authorities/subjects
/sh85059621|xGenetics.|0https://id.loc.gov/authorities/
subjects/sh99002134
650 7 Deafness|xGenetic aspects.|2fast|0https://id.worldcat.org/
fast/888577
650 7 Hearing disorders.|2fast|0https://id.worldcat.org/fast/
953415
650 7 Genetics.|2fast|0https://id.worldcat.org/fast/940117
655 4 Electronic books.
700 1 Toriello, Helga V.|0https://id.loc.gov/authorities/names/
n93804891
700 1 Smith, Shelley D.,|d1949-|0https://id.loc.gov/authorities/
names/n85045731
776 08 |iPrint version:|aToriello, Helga V.|tHereditary Hearing
Loss and Its Syndromes.|dOxford University Press USA 2013
|z1299708889
830 0 Oxford monographs on medical genetics ;|0https://
id.loc.gov/authorities/names/n42018416|vno. 63.
856 40 |uhttps://rider.idm.oclc.org/login?url=http://
search.ebscohost.com/login.aspx?direct=true&scope=site&
db=nlebk&AN=603923|zOnline eBook via EBSCO. Access
restricted to current Rider University students, faculty,
and staff.
856 42 |3Instructions for reading/downloading the EBSCO version
of this eBook|uhttp://guides.rider.edu/ebooks/ebsco
901 MARCIVE 20231220
948 |d20200122|cEBSCO|tEBSCOebooksacademic NEW 12-21,1-17
11948|lridw
994 92|bRID
