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Monosomy
Results: 9

#	Item
1	Turner Syndrome First description Henry Turner first described Turner syndrome in 1938, but it was not until 20 years later that the genetic basis of the syndrome was discovered. About 50% of clinically identified cases Add to Reading List Source URL: www.ssbp.org.uk Language: English - Date: 2015-05-13 15:34:16 Cytogenetics Biology Genodermatoses Chromosomal abnormalities Turner syndrome Neurological disorders X chromosome Autism Monosomy Health Genetics Syndromes
2	SOCIETY FOR THE STUDY OF BEHAVIOURAL PHENOTYPES An International Organisation The SSBP is a Registered Charity: Charity No:Turner syndrome Add to Reading List Source URL: www.qcidd.com.au Language: English - Date: 2013-02-13 00:06:40 Syndromes Biology Chromosomal abnormalities Genodermatoses Turner syndrome Neurological disorders X chromosome Aneuploidy Monosomy Genetics Cytogenetics Health
3	Why am I so short? A common reason for referral to the genetic counselling service is short stature. Patients often ask why they are short and if there is any treatment. To answer these questions, it is necessary to star Add to Reading List Source URL: www.dh.gov.hk Language: English - Date: 2013-04-08 23:51:23 Cytogenetics Chromosomal abnormalities Genodermatoses Turner syndrome Monosomy X chromosome Growth hormone treatment Aneuploidy Noonan syndrome Genetics Health Syndromes
4	Why am I so short? A common reason for referral to the genetic counselling service is short stature. Patients often ask why they are short and if there is any treatment. To answer these questions, it is necessary to star Add to Reading List Source URL: www.dh.gov.hk Language: English - Date: 2013-04-08 23:51:23 Cytogenetics Chromosomal abnormalities Genodermatoses Turner syndrome Monosomy X chromosome Growth hormone treatment Aneuploidy Noonan syndrome Genetics Health Syndromes
5	Patient Information: Medical Genomics -‐ Cytogenetics Laboratory (Patientt Label) 185 Berry St, Ste 290, Rm 2421 Add to Reading List Source URL: labmed.ucsf.edu Language: English - Date: 2014-10-29 12:51:17 Aneuploidy Amniocentesis Fluorescence in situ hybridization Deletion Metaphase Monosomy Chromosome Virtual karyotype Biology Genetics Cytogenetics
6	Cri-du-chat Syndrome: A Topical Overview Dennis J. Campbell, Ph.D Arkansas State University Mary Ester Carlin, MD FACMG Genetics and Developmental Center of the Southwest Add to Reading List Source URL: fivepminus.org Language: English - Date: 2004-10-20 14:42:28 Biology Rare diseases Cri du chat 5P Chromosome 5 Chromosome Monosomy Single transverse palmar crease Health Cytogenetics Syndromes
7	The mGluR5 antagonist AFQ056 does not affect methylation and transcription of the mutant FMR1 gene in vitro Add to Reading List Source URL: www.ncbi.nlm.nih.gov Language: English Diabetes Chromosomal abnormalities Cytogenetics 1p36 deletion syndrome Prader–Willi syndrome Monosomy Hyperinsulinism Contiguous gene syndrome Metabolic syndrome Health Syndromes Genodermatoses
8	Orphanet Journal of Rare Diseases BioMed Central Add to Reading List Source URL: www.ojrd.com Language: English Biology Cytogenetics Rare diseases Chromosomal abnormalities Cri du chat 5P Fryns Syndrome Chromosome 5 Monosomy Health Syndromes Genetics
9	PDF Document Add to Reading List Source URL: www.chromosome18.org Language: English - Date: 2010-05-18 10:24:40 Genetic disorders Chromosomal abnormalities Syndromes 18p- 18p Chromosome 18 Monosomy Contiguous gene syndrome Chromosome Genetics Biology Cytogenetics