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Syndromes / Medicine / Medical genetics / Copy-number variation / Molecular biology / DECIPHER / Deletion / 22q13 deletion syndrome / DiGeorge syndrome / Genetics / Biology / Health


Contribution of copy number variants (CNVs) to congenital, unexplained intellectual and developmental disabilities in Lebanese patients
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City

Carlsbad / Buckinghamshire / Loss / Paris / Gain / Foster City / Beirut / Marseille / /

Company

LG / Hoover / Thomson / Bernstein / Primer Express 3 Software / Affymetrix / Borthwick-Duffy SA / Squibb / Creative Commons / GE Healthcare / Suzuki / Yatsenko SA / designed using Primer Express 3 Software (ABI) / performed following the Affymetrix / Google / /

Country

France / United States / United Kingdom / Lebanon / /

Currency

pence / /

/

Facility

Saint Joseph University / American College of Medical Genetics / Hotel Dieu de France Hospital / Lebanese University / P18 M Xq28 Gain ID Terminal / Terminal De / /

IndustryTerm

non-specific products / software initiates studies / energy homeostasis / microarray analysis-based technologies / platforms hardware / online submission / /

MedicalCondition

retrognathism / microcephaly / ataxia / abnormal white matter signal / omphalocele / 1qter microdeletion syndrome / muscular ventricular septal defect / renal artery stenosis / DF / insulin-dependent diabetes mellitus / JE / Syndactyly / convergent strabismus / congenital abnormalities / seizures / developmental disabilities / learning disability / idiopathic autism / recessive disease / amblyopia / right thumb / Prenatally Diagnosed Choroidal Fissure Cyst / developmental disorders / Panhypopituitarism / blepharophimosis / obesity / Dawson G. Autism / cleft lip / speech delay / pulmonary atresia / distal 10q deletion syndrome / constipation / central depression / Ataxia / mild pachygyria / congenital heart defects / 1q44 syndrome / rare recessive diseases / mental retardation / unexplained mental retardation / recognizable clinical disorder / autism / cognitive impairment / hernia / seizure / exophthalmos / Mol Autism / cleft palate / hypotonia first weeks / kyphosis / tyrosinemia type II / future seizures / polymicrogyria / autosomal recessive disorders / epilepsy / strabismus / hypotonia / Tetralogy of Fallot / Irish multiplex schizophrenia / cataract / syndrome / /

MusicGroup

Gel / DNA / purified using the illustra TM GFX PCR DNA / /

OperatingSystem

Aix / /

Organization

Kearney H. American College of Medical Genetics and Genomics / Lebanese National Council for Scientific Research CNRS / Institutional Review Board / World Health Organization / Medical Genetics Unit / American Association on Intellectual and Developmental Disabilities / Medical Genetic Unit / Lebanese University / Beirut / Saint Joseph University / 6Neuropediatrics Department / USJ Council / /

Person

Van Bon / Jérôme Lejeune / Arch Pédiatrie / Burton H. Array / Joelle Abou / Van Coster / Enfants de La Timone / Ann Génétique / /

Position

pmol forward / Walker / author / Adam MP / /

Product

DV / /

ProvinceOrState

California / /

RadioStation

Haqq AM / /

Technology

Genomics / CRM / electrophoresis / hybridization / microarray analysis-based technologies / pdf / DNA Chip / DNA sequencing / SNP / DNA amplification / genotype / /

URL

http /

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