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Fragile X Syndrome
Fragile X syndrome
Overview
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Mental retardation
(16)
Down syndrome
Fetal alcohol syndrome
Phenylketonuria
American Association on Intellectual and Developmental Disabilities
Children Are Us Foundation
Children Are Us Foundation
Congenital hypothyroidism
Feeble-minded
Fetal Alcohol Spectrum Disorder
Imbecile
Lead poisoning
Lujan-Fryns syndrome
Mental retardation (Traditional terms)
Moron (psychology)
People with intellectual impairment
Richard O. Stimson
Up Syndrome
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Autism
Fragile X-associated tremor/ataxia syndrome
Rett syndrome
Cause of autism
Hyperlexia
Disability
(9)
Angelman syndrome
Prader Willi syndrome
Mental impairment
Myotonic dystrophy
Kennedy disease
Kennedy disease
Autism
Mental retardation
Fetal alcohol syndrome
Down syndrome
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Neurological disorders
Trinucleotide repeat
Friedreich ataxia
Familial dysautonomia
Tourette syndrome
Autism
Angelman syndrome
Kennedy disease
Pediatrics
Fifth disease
Lesch-nyhan syndrome
Down syndrome
Syndromes
(20)
Williams syndrome
Turner syndrome
Smith-Magenis syndrome
Klinefelter syndrome
Trisomy 18
Trisomy 18
Cri du chat syndrome
Sanfilippo syndrome
Proteus syndrome
Velo-cardio-facial syndrome
Treacher Collins syndrome
Syndrome
Noonan syndrome
Rett syndrome
Angelman syndrome
Prader Willi syndrome
Fetal alcohol syndrome
Lesch-nyhan syndrome
Familial dysautonomia
Down syndrome
Tourette syndrome
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Genetic disorders
(35)
Smith-lemli-opitz syndrome
X-linked dominant
Tuberous sclerosis
Langer-giedion syndrome
Facioscapulohumeral muscular dystrophy
Facioscapulohumeral muscular dystrophy
Rubinstein-taybi syndrome
Chromosome abnormality
Fructosemia
Nevoid basal cell carcinoma syndrome
Tay Sachs disease
Microdeletion
Familial mediterranean fever
Genetic condition
Barth syndrome
Rett syndrome
Trinucleotide repeat
Angelman syndrome
Williams syndrome
Friedreich ataxia
Prader Willi syndrome
Turner syndrome
Smith-Magenis syndrome
Klinefelter syndrome
Lesch-nyhan syndrome
Trisomy 18
Down syndrome
Cri du chat syndrome
Myotonic dystrophy
Sanfilippo syndrome
Velo-cardio-facial syndrome
Phenylketonuria
Treacher Collins syndrome
Noonan syndrome
Kennedy disease
Tourette syndrome
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Diseases and disorders
(48)
X syndrome
Factor xii deficiency
X-linked mental retardation
Fibrocystic breast disease
Macroorchidism
Macroorchidism
Premature ovarian failure
Frambesia
Folliculitis
Uniparental disomy
Fatty liver
Factor V Leiden thrombophilia
Funnel chest
Female infertility
Floating harbor syndrome
Menkes syndrome
Fox Fordyce disease
Sturge-Weber
Autism
Mental retardation
Fifth disease
Angelman syndrome
Friedreich ataxia
Prader Willi syndrome
Fetal alcohol syndrome
Klinefelter syndrome
Tuberous sclerosis
Lesch-nyhan syndrome
Trisomy 18
Familial dysautonomia
Langer-giedion syndrome
Down syndrome
Facioscapulohumeral muscular dystrophy
Cri du chat syndrome
Myotonic dystrophy
Sanfilippo syndrome
Chromosome abnormality
Fructosemia
Proteus syndrome
Nevoid basal cell carcinoma syndrome
Tay Sachs disease
Hyperlexia
Velo-cardio-facial syndrome
Phenylketonuria
Noonan syndrome
Kennedy disease
Familial mediterranean fever
Tourette syndrome
Barth syndrome
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Genetics
(13)
X linked
Mosaicism
Chromosome analysis
X chromosome inactivation
Mutation
Mutation
The Sherman paradox
Medical genetics
DNA marker
X-linked recessive
Gene
Genetic disorders
Microdeletion
Genetic condition
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Childhood psychiatric disorders
(39)
Language delay
Abandoned child syndrome
Adjustment disorder
Adopted child syndrome
Asperger syndrome
Asperger syndrome
Attachment therapy
Attention-deficit hyperactivity disorder controversies
Autism
Autism Diagnostic Observation Schedule
Bipolar disorder in children
Child and Adolescent Mental Health Services
Child psychopathology
Child pyromaniac
Childhood disintegrative disorder
Conduct disorder
Diagnosis of Asperger syndrome
Disorder of written expression
Encopresis
Expressive language disorder
Gilliam Asperger's Disorder Scale
Hebrew Academy for Special Children
Learning disability
List of stutterers
Mental retardation
Neurodevelopmental disorder
Oppositional defiant disorder
PANDAS
Parent Management Training
Pervasive developmental disorder
Pica (disorder)
Regressive autism
School refusal
Selective mutism
Sluggish cognitive tempo
Specific developmental disorder
Stephen Faraone
Stereotypic movement disorder
Stranger anxiety
Tourette syndrome
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Cytogenetics
(20)
Chromosome
Fragile site
X chromosome
Aneuploidy
Autosome
Autosome
Chromosomal translocation
Chromosome abnormality
Colcemid
Fluorescent in situ hybridization
Germ plasm
Homologous chromosome
Karyotype
Monosomy
Ploidy
Pseudoautosomal region
Robertsonian translocation
Synapsis
Tetrasomy
Trisomy
Uniparental disomy
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Symptoms
Large testicles
Motormental retardation
Prominent forehead
Large forehead
Mental retardation
Mental impairment
Nervous system disease
(8)
MASA syndrome
Norrie disease
Ocular albinism
Ocular albinism type 1
Pelizaeus-- Merzbacher disease
Pelizaeus-- Merzbacher disease
X-linked alpha thalassemia mental retardation syndrome
X-linked spinal muscular atrophy 2
X-Linked mental retardation
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See also
(20)
FMR1
Friedreich
MGLUR5
The Canadian Grenadier Guards
The Fragile
The Fragile
Dendritic spines
M.I.N.D. Institute
Picower Institute for Learning and Memory
MeCP2
Genetic counseling
Pervasive developmental disorders
Foreign exchange station
Fenobam
High-functioning autism
Letters by alphabet
Testicle
Www.nfxf.org
Xq28
Fluoridation
Chromosome 21
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