Chromosome 1 - PDFSEARCH.IO - Document Search Engine

Chromosome 1
Results: 219

#	Item
171	Teacher Preparation Notes for Dragon Genetics -- Independent Assortment and Genetic Linkage by Dr. Ingrid Waldron and Dr. Jennifer Doherty, Department of Biology, University of Pennsylvania, 2011 1 Add to Reading List Source URL: serendip.brynmawr.edu Language: English - Date: 2011-01-18 15:18:40 Cellular processes Molecular genetics Cytogenetics Genetic linkage Chromosomal crossover Meiosis Homologous chromosome Dominance Genetic recombination Biology Genetics Classical genetics
172	1 In the first half of the 20th century, Dr. Guido Fanconi published detailed clinical descriptions of several heritable human diseases. Two disease syndromes were named after him: Fanc Add to Reading List Source URL: www.basenji.org Language: English - Date: 2011-10-13 19:18:54 Basenji Fanconi anemia Guido Fanconi Meiosis Chromosome Biology Cell biology Fanconi syndrome
173	Experimental Cell Research 252, 273–[removed]Article ID excr[removed], available online at http://www.idealibrary.com on Isolation and Characterization of a Near-Haploid Human Cell Line Maciej Kotecki, 1,2 P. Sanjee Add to Reading List Source URL: www.cochranlab.org Language: English - Date: 2005-01-04 14:31:04 Classical genetics Cell cycle Developmental biology Ploidy Karyotype Chromosome Polyploid Somatic cell Cell growth Biology Genetics Cytogenetics
174	Frequently Asked Questions 1. If no members of my family are affected by PWS, can I still have a child with the condition? Yes. The majority of cases of PWS occur in families where there has been no history of the condi Add to Reading List Source URL: www.mrds.org.my Language: English - Date: 2011-03-08 01:10:09 Genodermatoses Syndromes Medical genetics Prader–Willi syndrome Chromosome 15 Growth hormone treatment Obesity Genetic disorder Genetic testing Health Medicine Biology
175	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 Add to Reading List Source URL: www.mrds.org.my Language: English - Date: 2011-03-08 01:09:26 Syndromes Chromosomal abnormalities Chromosomes Chromosome abnormality Aneuploidy Chromosome Karyotype Chromosomal translocation Edwards syndrome Genetics Biology Cytogenetics
176	Study Title: Validation of Card-PCR analysis through programmed imatinib interruption in PCR negative CML patients. 1. Background and introduction 1.1 Add to Reading List Source URL: www.ilte-cml.org Language: English - Date: 2010-08-23 16:57:02 Orphan drugs Piperazines Myeloid leukemia Pyrimidines Chronic myelogenous leukemia Pyridines Philadelphia chromosome Imatinib Abl gene Medicine Oncology Organic chemistry
177	TAXON 56 (1) • February 2007: 209 Marhold • IAPT/IOPB chromosome data 3 I O PB CO LU M N Edited by Karol Marhold & Gonzalo Nieto Feliner Add to Reading List Source URL: www.iopb.org Language: English - Date: 2007-07-30 05:02:24 Cuphea Lythraceae 2N
178	TAXON 58 (1) • February 2009: 181–183 Marhold • IAPT/IOPB chromosome data 7 I O PB CO LU M N Edited by Karol Marhold & Ilse Breitwieser Add to Reading List Source URL: www.iopb.org Language: English - Date: 2009-03-27 14:45:43 Colchicum Colchicaceae Botany Colchicum bulbocodium
179	Marche des Maladies Rares – Alliance Maladies Rares Orphanet Report Series Rare Diseases collection December Add to Reading List Source URL: www.orpha.net Language: English - Date: 2013-10-21 08:05:01 Genetic genealogy Rare diseases 17q21.31 microdeletion syndrome 3q29 microdeletion syndrome Alström syndrome Down syndrome Turner syndrome Myelodysplastic syndrome Chromosome 1 Health Syndromes Genetics
180	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