41![3. KARYOTYPE SCREEN REPORT REPORT WITH SUMMARY OF CHROMOSOME COUNTS & KARYOTYPE OF FIVE METAPHASE CELLS 3. KARYOTYPE SCREEN REPORT REPORT WITH SUMMARY OF CHROMOSOME COUNTS & KARYOTYPE OF FIVE METAPHASE CELLS](https://www.pdfsearch.io/img/211c960367e484fa9c8f5e3cd7245b83.jpg) | Add to Reading ListSource URL: www.tcag.caLanguage: English - Date: 2012-08-20 15:12:04
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42![Tuesday, February 28, 8:00AM-12:00PM Plenary Session Chromosome Abnormalities Moderator: Angela E. Lin, Harvard Medical School, and MassGeneral Hospital for Children, Boston, MA Syndrome Review I: Common Trisomies and Se Tuesday, February 28, 8:00AM-12:00PM Plenary Session Chromosome Abnormalities Moderator: Angela E. Lin, Harvard Medical School, and MassGeneral Hospital for Children, Boston, MA Syndrome Review I: Common Trisomies and Se](https://www.pdfsearch.io/img/97dc2a90e247e9f0ff4713ac69625159.jpg) | Add to Reading ListSource URL: www.nbdpn.orgLanguage: English - Date: 2012-04-16 14:13:04
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43![Tuesday, February 28, 8:00AM-12:00PM Plenary Session Chromosome Abnormalities Moderator: Angela E. Lin, Harvard Medical School, and MassGeneral Hospital for Children, Boston, MA Syndrome Review II: Common Deletion/Microd Tuesday, February 28, 8:00AM-12:00PM Plenary Session Chromosome Abnormalities Moderator: Angela E. Lin, Harvard Medical School, and MassGeneral Hospital for Children, Boston, MA Syndrome Review II: Common Deletion/Microd](https://www.pdfsearch.io/img/6b4bb6aea9b46c228d1a399a9168ed8b.jpg) | Add to Reading ListSource URL: www.nbdpn.orgLanguage: English - Date: 2012-04-16 14:26:49
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44![Fingering the culprit. Extra copies of one gene cause a form of Charcot-Marie-Tooth disease, a neuropathy that affects the feet and hands. GENOMICS Fingering the culprit. Extra copies of one gene cause a form of Charcot-Marie-Tooth disease, a neuropathy that affects the feet and hands. GENOMICS](https://www.pdfsearch.io/img/2c8d522f64fb8ad368d04ab2973769e3.jpg) | Add to Reading ListSource URL: www.tcag.caLanguage: English - Date: 2012-01-18 10:05:54
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45![Paper published in Radiation Research Paper published in Radiation Research](https://www.pdfsearch.io/img/1e664c9b79ea61fd03a4585f691d1649.jpg) | Add to Reading ListSource URL: www.rerf.or.jpLanguage: English - Date: 2013-04-23 04:30:16
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46![Microsoft PowerPoint - Powerpoint_Genomicinstability.ppt [Compatibility Mode] Microsoft PowerPoint - Powerpoint_Genomicinstability.ppt [Compatibility Mode]](https://www.pdfsearch.io/img/32f3f0a8dae94d87bc7a1d0a5a78d765.jpg) | Add to Reading ListSource URL: lowdose.energy.govLanguage: English - Date: 2012-03-05 16:55:52
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47![Frequently Asked Questions 1. If no members of my family have a chromosomal anomaly can I still have a child with the condition? Yes. There are two ways chromosomal anomalies occur in an individual, through inheritance Frequently Asked Questions 1. If no members of my family have a chromosomal anomaly can I still have a child with the condition? Yes. There are two ways chromosomal anomalies occur in an individual, through inheritance](https://www.pdfsearch.io/img/e0c262f91335c119ca1a4755851b0021.jpg) | Add to Reading ListSource URL: www.mrds.org.myLanguage: English - Date: 2011-03-08 01:09:26
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48![Parinti si o sora sanatoasa Parinti si o sora sanatoasa](https://www.pdfsearch.io/img/43ceadbe6ffafe0f51cef0de170bf939.jpg) | Add to Reading ListSource URL: www.ncbi.nlm.nih.govLanguage: English |
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49![The mGluR5 antagonist AFQ056 does not affect methylation and transcription of the mutant FMR1 gene in vitro The mGluR5 antagonist AFQ056 does not affect methylation and transcription of the mutant FMR1 gene in vitro](https://www.pdfsearch.io/img/a60980d624b93e26b6dd4720afba6be7.jpg) | Add to Reading ListSource URL: www.ncbi.nlm.nih.govLanguage: English |
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50![The incidence and type of chromosomal translocations from prenatal diagnosis of 3800 patients in Republic of Macedonia The incidence and type of chromosomal translocations from prenatal diagnosis of 3800 patients in Republic of Macedonia](https://www.pdfsearch.io/img/f281e3ae6edfe510ac9320eeb7739f7a.jpg) | Add to Reading ListSource URL: www.ncbi.nlm.nih.govLanguage: English |
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