000 | 05213cam a2200733 a 4500 | ||
---|---|---|---|
001 | ocn760070179 | ||
003 | OCoLC | ||
005 | 20221128212904.0 | ||
006 | m d | ||
007 | cr un||||a|a|| | ||
008 | 111109s2008 caua ob 001 0 eng d | ||
040 |
_aOCLCE _beng _epn _cOCLCE _dOCLCQ _dOCLCF _dOCLCO _dEBLCP _dE7B _dN$T _dOCLCQ _dYDXCP _dOCLCQ _dD6H _dAZK _dCCO _dPIFAG _dZCU _dOCLCO _dMERUC _dOCLCO _dU3W _dCOCUF _dSTF _dOCLCQ _dICG _dVT2 _dOCLCQ _dWYU _dOCLCA _dDKC _dOCLCO _dOCLCQ _dUX1 _dHS0 _dUWK _dADU _dOCLCQ _dOCLCA _dOCLCQ _dOCLCA _dUKCRE _dOCLCQ _dTUHNV _dOCLCO _dREDDC _dOCLCQ _dS2H _dOCLCO |
||
016 | 7 |
_a101315706 _2DNLM |
|
019 |
_a919318002 _a961530196 _a974382392 _a991964649 _a1017995130 _a1023009380 _a1037761785 _a1045045179 _a1055385851 _a1066455312 _a1081287705 _a1101730491 _a1109008618 _a1110388484 _a1112871712 _a1119027551 _a1153450404 _a1228618586 _a1243605555 _a1257363868 _a1289517652 |
||
020 |
_a9781597568463 _q(electronic bk.) |
||
020 |
_a1597568465 _q(electronic bk.) |
||
020 |
_z9781597562584 _q(pbk.) |
||
020 |
_z1597562580 _q(pbk.) |
||
035 |
_a991919 _b(N$T) |
||
035 |
_a(OCoLC)760070179 _z(OCoLC)919318002 _z(OCoLC)961530196 _z(OCoLC)974382392 _z(OCoLC)991964649 _z(OCoLC)1017995130 _z(OCoLC)1023009380 _z(OCoLC)1037761785 _z(OCoLC)1045045179 _z(OCoLC)1055385851 _z(OCoLC)1066455312 _z(OCoLC)1081287705 _z(OCoLC)1101730491 _z(OCoLC)1109008618 _z(OCoLC)1110388484 _z(OCoLC)1112871712 _z(OCoLC)1119027551 _z(OCoLC)1153450404 _z(OCoLC)1228618586 _z(OCoLC)1243605555 _z(OCoLC)1257363868 _z(OCoLC)1289517652 |
||
037 | _nTitle subscribed to via ProQuest Academic Complete | ||
042 | _adlr | ||
060 | 4 | _a2008 D-153 | |
060 | 4 |
_aQZ 50 _bR655m 2008 |
|
072 | 7 |
_aHEA _x039000 _2bisacsh |
|
072 | 7 |
_aMED _x014000 _2bisacsh |
|
072 | 7 |
_aMED _x022000 _2bisacsh |
|
072 | 7 |
_aMED _x112000 _2bisacsh |
|
072 | 7 |
_aMED _x045000 _2bisacsh |
|
049 | _aMAIN | ||
100 | 1 | _aRobin, Nathaniel. | |
245 | 1 | 0 |
_aMedical genetics : _bits application to speech, hearing, and craniofacial disorders _c _h[E-Book] |
260 |
_aSan Diego : _bPlural Pub., _c2008. |
||
300 |
_a1 online resource (xii, 182 pages) : _billustrations (chiefly color) |
||
336 |
_atext _btxt _2rdacontent |
||
337 |
_acomputer _bc _2rdamedia |
||
338 |
_aonline resource _bcr _2rdacarrier |
||
347 | _adata file | ||
490 | 1 | _aGenetic syndromes and communication disorders series | |
504 | _aIncludes bibliographical references and index. | ||
505 | 0 | _aGenetics professionals: an overview / Nathaniel Robin -- Genetic inheritance: Mendelian, non-Mendelian and multi-factorial / Nathaniel H. Robin -- Evaluation of the patient with a congenital anomaly / Nathaniel H. Robin -- Classification of birth defects / Nathaniel H. Robin and Marni Falk -- Genetic testing: cytogenetics, biochemical genetics and molecular genetics / Nathaniel H. Robin and Edward J. Lose -- Ethical issues in genetic testing / Nathaniel H. Robin -- Genetic counseling and your practice / Nathaniel H. Robin and Sandra Prucka -- Genetics and hearing loss / Nathaniel H. Robin -- Craniofacial genetics I: cleft lip and cleft palate / Nathaniel H. Robin -- Craniofacial genetics II: craniosynostosis and related syndromes / Nathaniel H. Robin. | |
588 | 0 | _aPrint version record. | |
506 |
_3Use copy _fRestrictions unspecified _2star _5MiAaHDL |
||
520 | _aThis book reviews the rapidly developing field medical genetics from theories to its implications for clinical practice. This book covers the whole field of medical genetics from a general overview of the profession to details of effective treatment of patients with common and esoteric genetic disorders--including birth defects, hearing loss, oro-facial clefting, craiosynostosis, and much more. Crucially, as issues surrounding breakthroughs in understanding and development of new technologies in genetics have risen to the fore of the cultural consciousness, it gives coverage to the many ethical questions raised. | ||
533 |
_aElectronic reproduction. _b[Place of publication not identified] : _cHathiTrust Digital Library, _d2011. _5MiAaHDL |
||
538 |
_aMaster and use copy. Digital master created according to Benchmark for Faithful Digital Reproductions of Monographs and Serials, Version 1. Digital Library Federation, December 2002. _uhttp://purl.oclc.org/DLF/benchrepro0212 _5MiAaHDL |
||
583 | 1 |
_adigitized _hHathiTrust Digital Library _lcommitted to preserve _2pda _5MiAaHDL |
|
546 | _aEnglish. | ||
590 | _aWorldCat record variable field(s) change: 650 | ||
650 | 0 | _aMedical genetics. | |
650 | 0 | _aGenetic disorders. | |
650 | 0 | _aGenetic screening. | |
650 | 1 | 2 | _aGenetics, Medical |
650 | 2 | 2 | _aGenetic Diseases, Inborn |
650 | 2 | 2 | _aGenetic Testing |
830 | 0 | _aGenetic syndromes and communication disorders series. | |
856 | 4 | 0 |
_uhttps://search.ebscohost.com/login.aspx?custid=ns123844&authtype=ip,shib&direct=true&scope=site&db=nlebk&db=nlabk&AN=991919 _yKingston Hospital NHS Foundation Trust OpenAthens account holders click here for access |
938 |
_aProQuest Ebook Central _bEBLB _nEBL2051350 |
||
938 |
_aebrary _bEBRY _nebr11056638 |
||
938 |
_aEBSCOhost _bEBSC _n991919 |
||
938 |
_aYBP Library Services _bYANK _n12423017 |
||
942 | _n0 | ||
994 |
_a92 _bN$T |
||
999 |
_c92179 _d92179 |