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Chromosome 17
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11	VOL. 17,193l BOTANY: B.McCLINTOCK Add to Reading List Source URL: profiles.nlm.nih.gov Language: English - Date: 2001-06-05 18:56:02 Classical genetics Cellular processes Molecular genetics Chromosome Ploidy Homologous chromosome Genetic linkage Meiosis Y chromosome Biology Genetics Cytogenetics
12	c Indian Academy of Sciences RESEARCH NOTE Concurrent psu dic(21)(q22.3) and t(13;17)(q14.1;p12) in a mosaic Add to Reading List Source URL: www.ias.ac.in Language: English - Date: 2014-05-01 12:00:31 Chromosomes Dicentric chromosome Chromosomal translocation Robertsonian translocation X chromosome Turner syndrome Down syndrome Chromosome 21 Meiosis Genetics Biology Cytogenetics
13	ESSAY CORRECTED 17 FEBRUARY 2012; SEE LAST PAGE GE PRIZE ESSAY Add to Reading List Source URL: unlockinglifescode.org Language: English - Date: 2014-07-09 10:32:06 Genomics Molecular biology Fractal globule Fractals Full genome sequencing Human genome Chromatin Chromosome Shotgun sequencing Biology Genetics DNA
14	Knowledge is Hope neWsletter January[removed]Volume 17, Issue 1 Add to Reading List Source URL: vcfsef.org Language: English - Date: 2013-07-10 06:35:00 Syndromes Sleep disorders Communication disorders Speech DiGeorge syndrome Chromosome 22 Obstructive sleep apnea Speech sound disorder Hypernasal speech Medicine Health Speech and language pathology
15	Microsoft PowerPoint - Elsea and Williams figures1 and 3 Add to Reading List Source URL: www.prisms.org Language: English - Date: 2011-05-28 07:31:16 Genetics Rare diseases Smith–Magenis syndrome Congenital disorders Medical genetics RAI1 Potocki-Lupski syndrome Chromosome 17 DECIPHER Health Syndromes Biology
16	"Smith-Magenis Syndrome". In: Encyclopedia of Life Sciences (ELS) Add to Reading List Source URL: www.prisms.org Language: English - Date: 2011-03-17 21:28:57 Smith–Magenis syndrome RAI1 Potocki-Lupski syndrome Haploinsufficiency Prader–Willi syndrome Chromosome 17 Aneuploidy Medical genetics Non allelic homologous recombination Health Syndromes Medicine
17	European Journal of Human Genetics[removed], 412–421 & 2008 Nature Publishing Group All rights reserved[removed] $30.00 Add to Reading List Source URL: www.nature.com Language: English - Date: 2010-01-19 10:40:20 RAI1 Potocki-Lupski syndrome Prader–Willi syndrome Haploinsufficiency Chromosome 17 DiGeorge syndrome Williams syndrome TNFRSF13B Joubert syndrome Health Syndromes Smith–Magenis syndrome
18	CMYK 17_2_06_Siljak_Yakovlev_&_al.indd Add to Reading List Source URL: www.bio.bas.bg Language: English - Date: 2011-08-30 13:10:44 Genomics Classical genetics Micromeria Genome size C-value Chromosome Genome Plant DNA C-values Database DNA Genetics Biology Cytogenetics
19	JMed Genet 1991; 28: 1-5 I Add to Reading List Source URL: www.ncbi.nlm.nih.gov Language: English Health Charcot–Marie–Tooth disease Hereditary motor and sensory neuropathy Dejerine–Sottas disease Chromosome 17 Chromosome 1 X-linked recessive inheritance Genetic linkage Pes cavus Neurological disorders Genetics Biology
20	Chapter 17 The Genetics of Language and Farming Spread in India Toomas Kivisild, Siiri Rootsi, Mait Metspalu, Ene Metspalu, Add to Reading List Source URL: www.ebc.ee Language: English - Date: 2003-12-05 11:44:19 Biology Pleistocene Haplogroup N Haplogroup Macro-haplogroup L Toomas Kivisild Genetics and archaeogenetics of South Asia Human Y-chromosome DNA haplogroup Recent single origin hypothesis Human evolution Genetics