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Extra Chromosome
Extra chromosome
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Cytogenetics
(19)
Autosomes
Chromosomal translocation
Chromosome
Chromosome abnormality
Chromosome number
Chromosome number
Homologous chromosomes
Karyotype
Monosomy
Robertsonian translocation
Trisomy
X chromosome
Colcemid
Fluorescent in situ hybridization
Fragile sites
Germ plasm
Pseudoautosomal region
Synapsis
Tetrasomy
Uniparental disomy
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Genetic disorders
(26)
Patau syndrome
Down syndrome
Edwards syndrome
Klinefelter syndrome
XYY
XYY
Turner syndrome
22q11.2 deletion syndrome
Cri du chat
Philadelphia chromosome
Triple X syndrome
Trisomy 9
Wolf-Hirschhorn syndrome
Isodicentric chromosome 15 syndrome
Microphthalmia
XXXXY
Microcephaly
Genetic condition
Trisomy 16
Extra fingers
Warkany syndrome 2
XXYY
Angelman syndrome
Polysomy
Trisomy
Chromosome abnormality
Monosomy
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Diseases and disorders
(23)
Mental retardation
Xxy males
Poor muscle tone
Meningomyelocele
Micrognathia
Micrognathia
Polyploid
Cat eye syndrome
Chromosome 9 trisomy mosaic
Heart defects
Patau syndrome
Chromosome abnormality
Down syndrome
Edwards syndrome
Klinefelter syndrome
XYY
22q11.2 deletion syndrome
Cri du chat
Triple X syndrome
Trisomy 9
Microphthalmia
Microcephaly
Extra fingers
Angelman syndrome
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Genetics
(15)
Chromosomes
Mosaicism
Human chromosomes
Nondisjunction
X inactivation
X inactivation
Satellite chromosome
Genes
Molecular cytogenetics
B chromosome
Genetic disorders
XYY
Chromosome analysis
Homologous chromosomes
Genetic condition
XXYY
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Syndromes
(13)
Congenital rubella syndrome
Patau syndrome
Down syndrome
Edwards syndrome
Klinefelter syndrome
Klinefelter syndrome
XYY
Turner syndrome
22q11.2 deletion syndrome
Cri du chat
Triple X syndrome
Wolf-Hirschhorn syndrome
Warkany syndrome 2
Angelman syndrome
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Congenital disorders
(8)
Holoprosencephaly
Malformations
Genetic disorders
Meningomyelocele
Microcephaly
Microcephaly
Extra fingers
Cat eye syndrome
Congenital rubella syndrome
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Down syndrome
(11)
Health aspects of Down syndrome
People with Down syndrome
Trisomy 21
Centro Ann Sullivan del Perú
Down syndrome (History)
Down syndrome (History)
Down's Syndrome Scotland
Genetic origins of Down syndrome
National Down Syndrome Society
Research of Down syndrome-related genes
The Specials (internet TV show)
Up Syndrome
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Molecular genetics
Chromatids
Heterochromatin
Meiosis
Euchromatin
X inactivation
Symptoms
Low set ears
Upward slanting eyes
Broad short hands
Mental retardation
Poor muscle tone
Heart defects
Chromosomes
(57)
Centromere
Chromosome 11
Chromosome 13
Chromosome 15
Chromosome 16
Chromosome 16
Chromosome 17
Chromosome 18
Chromosome 21
Chromosome 22
Chromosome 4
Chromosome 5
Chromosome 9
Marker chromosome
Short arm
Small supernumerary marker chromosome
Y chromosome
AZF1
Allosome
Autosomes
Chromatids
Chromomere
Chromosomal inversion
Chromosomal translocation
Chromosome
Chromosome 1 (human)
Chromosome 10 (human)
Chromosome 12 (human)
Chromosome 14 (human)
Chromosome 19 (human)
Chromosome 2 (human)
Chromosome 20 (human)
Chromosome 3 (human)
Chromosome 6 (human)
Chromosome 7 (human)
Chromosome 8 (human)
Chromosome abnormality
Chromosome conformation capture
Chromosome engineering
Chromosome regions
Chromosome segregation
Derivative chromosome
Dicentric chromosome
Dyad (biology)
G banding
Human β-globin locus
Inchrosil
Isochromosome
Karyotype
Lampbrush chromosome
Personalized medicine
Proline-Rich Coiled Coil 1
Ring chromosome
Satellite chromosome
Subtelomere
Syntelic
Telomere
X chromosome
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See also
(20)
Sex chromosome
Cells
Reproductive cells
Human chromosome
Maternal age
Maternal age
Klaus Patau
Chorionic villus sampling
Brushfield spots
Amniocentesis
Meiosis I
John Langdon Down
Abnormal number
Diploid
Delayed speech
Metaphase
Sperm cell
World Down Syndrome Day
Genes on chromosome 21
Chromosome (genetic algorithm)
Kinetochores
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