000 | 03015nam a22007337a 4500 | ||
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003 | KOHA_MİRAKIL | ||
005 | 20221103135255.0 | ||
008 | 211117d2022 enkod||| |||| 00| 0 eng d | ||
020 | _a9780702079665 | ||
040 |
_aCY-NiCIU _beng _cCY-NiCIU _erda |
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041 | _aeng | ||
082 | 0 | 0 |
_a616.042 _bT97 2022 |
100 | 1 |
_aTurnpenny, Peter D. _eauthor |
|
245 | 1 | 0 |
_aEmery's Elements of Medical Genetics and Genomics / _cPeter D. Turnpenny, Sian Ellard, Ruth Cleaver |
250 | _aEDITION: 16 | ||
264 | 1 |
_aEdinburg : _bELSEVIER, _c2022. |
|
300 |
_aix,435 pages : _bphotos, tables ; _c28 cm |
||
336 |
_2rdacontent _atext _btxt |
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337 |
_2rdamedia _aunmediated _bn |
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338 |
_2rdacarrier _avolume _bnc |
||
500 | _a11 copies | ||
590 | _aMedical Genetics | ||
590 | _aMDCN126, MDCN226 | ||
650 | 0 | _aMedical genetics | |
700 | 1 |
_aEllard, Sian _eauthor |
|
700 | 1 |
_aCleaver, Ruth _eauthor |
|
942 |
_2ddc _cBK |
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505 | 1 |
_g1 _tThe History and Impact of Genetics in Medicine |
|
505 | 1 | _tThe Scientific Basis of Human Genetics | |
505 | 1 |
_g10 _tThe Cellular and Molecular Basis of Inheritance |
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505 | 1 |
_g26 _tChromosomes and Cell Division |
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505 | 1 |
_g44 _tFinding the Causes of Monogenic Disorders By Identifying Disease Genes |
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505 | 1 |
_g51 _tLaboratory Techniques for Diagnosis of Monogenic Disorder |
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505 | 1 |
_g67 _tPatterns of Inheritance |
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505 | 1 |
_g84 _tPopulation and Mathematical Genetics |
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505 | 1 |
_g96 _tRisk Calculation |
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505 | 1 |
_g105 _tDevelopmental Genetics |
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505 | 1 | _tGenetics in Medicine and Genetics | |
505 | 1 |
_g136 _tCommon Disease. Polygenic and Multifactorial Genetics |
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505 | 1 |
_g151 _tScreening for Genetic Disease |
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505 | 1 |
_g161 _tHemoglobin and the Hemoglobinopathies |
|
505 | 1 |
_g171 _tImmunogenetics |
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505 | 1 |
_g184 _tThe Genetics of Cancer and Cancer Genetics |
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505 | 1 |
_g210 _tPharmacogenomics, Precision Medicine, and the Treatment of Genetic Disease |
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505 | 1 | _tClinical Genetics, Counseling and Ethics | |
505 | 1 |
_g227 _tCongenital Abnormalities Dysmorphic Syndromes and Intellectual Disability |
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505 | 1 |
_g250 _tChromosome Disorder |
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505 | 1 |
_g271 _tInborn Errors of Metabolism |
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505 | 1 |
_g289 _tMainstream Monogenic Disorders |
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505 | 1 |
_g322 _tPrenatal Testing and Reproductive Genetics |
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505 | 1 |
_g338 _tGenetic Counseling |
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505 | 1 |
_g345 _tEthical and Legal Issues in medical Genetics |
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505 | 1 |
_g355 _tGlossary |
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505 | 1 |
_g372 _tAppendix : Websites and Clinical Databases |
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505 | 1 |
_g374 _tMultiple Choice Questions |
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505 | 1 |
_g382 _tCase-Based Questions |
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505 | 1 |
_g387 _tMultiple -Choice Answers |
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505 | 1 |
_g396 _tCase-Based Answers and Discussion |
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505 | 1 |
_g403 _tClinical Scenario Answers and Discussion |
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505 | 0 |
_g412 _tIndex |
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999 |
_c283224 _d283224 |