| 000 | 02941cam a2200613Mi 4500 | ||
|---|---|---|---|
| 001 | on1099562223 | ||
| 003 | OCoLC | ||
| 005 | 20221128213614.0 | ||
| 006 | m e d | ||
| 007 | cr cn||||m|||a | ||
| 008 | 190417s2018 nyu fob 001 0 eng d | ||
| 040 |
_aNYMPP _beng _erda _epn _cNYMPP _dOCLCO _dUKAHL _dOCLCF _dOCLCQ _dN$T |
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| 020 | _a1944749705 | ||
| 020 |
_a9781944749705 _q(electronic bk.) |
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| 020 |
_z9781944749699 _q(print) |
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| 035 |
_a2095746 _b(N$T) |
||
| 035 | _a(OCoLC)1099562223 | ||
| 049 | _aMAIN | ||
| 100 | 1 |
_aEckdahl, Todd T., _eauthor. |
|
| 245 | 1 | 0 |
_aNewborn screening for genetic disorders : _bexperiments on plant hybridization _c _h[E-Book] |
| 250 | _aFirst edition. | ||
| 264 | 1 |
_aNew York, New York (222 East 46th Street, New York, NY 10017) : _bMomentum Press, _c2018. |
|
| 300 | _a1 online resource (1 PDF (89 pages)) | ||
| 336 |
_atext _btxt _2rdacontent |
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| 337 |
_acomputer _bc _2isbdmedia |
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| 338 |
_aonline resource _bcr _2rdacarrier |
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| 490 | 1 | _aHuman diseases and conditions collection | |
| 504 | _aIncludes bibliographical references and index. | ||
| 505 | 0 | _aChapter 1. Symptoms and diagnosis -- Chapter 2. Causes and contributing factors -- Chapter 3. Treatment and therapy -- Chapter 4. Future prospects. | |
| 520 | 3 | _aThis book describes newborn screening as a public health program for the early detection of genetic disorders. It presents the recommended uniform screening panel (RUSP), a list of genetic disorders recommended by the U.S. government for states to include in new- born screening programs. The author describes the categorization of RUSP genetic disorders, discusses the symptoms and health complications of examples from each category, and explains clinical laboratory tests used for newborn screening. | |
| 588 | 0 | _aPDF viewed 04/17/2019. | |
| 590 | _aAdded to collection customer.56279.3 | ||
| 650 | 0 | _aMedical screening. | |
| 650 | 0 |
_aNewborn infants _xDiseases _xDiagnosis. |
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| 653 | _aAmino acid metabolism disorders. | ||
| 653 | _aAutosomal dominant. | ||
| 653 | _aAutosomal recessive. | ||
| 653 | _aEndocrine disorders. | ||
| 653 | _aFatty acid oxidation disorders. | ||
| 653 | _aGenetic disease. | ||
| 653 | _aHemoglobin disorders. | ||
| 653 | _aIncomplete dominance. | ||
| 653 | _aNewborn screening. | ||
| 653 | _aOrganic acid disorders. | ||
| 653 | _aRecommended universal screening panel. | ||
| 653 | _aSex-linked inheritance. | ||
| 830 | 0 | _aHuman diseases and conditions collection. | |
| 856 | 4 | 0 |
_uhttps://search.ebscohost.com/login.aspx?custid=ns123844&authtype=ip,shib&direct=true&scope=site&db=nlebk&db=nlabk&AN=2095746 _yKingston Hospital NHS Foundation Trust OpenAthens account holders click here for access |
| 938 |
_aAskews and Holts Library Services _bASKH _nBDZ0039994639 |
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| 938 |
_aMomentum Press _bNYMP _n9781944749705 |
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| 938 |
_aEBSCOhost _bEBSC _n2095746 |
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| 942 | _n0 | ||
| 994 |
_a92 _bN$T |
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| 999 |
_c93287 _d93287 |
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