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Partial Trisomy
Partial trisomy
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Related in the Kosmos
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Cytogenetics
(19)
Autosomal
Chromosomal translocation
Chromosome
Chromosome disorders
Fluorescence in situ hybridization
Fluorescence in situ hybridization
Karyotype
Mixoploidy
Monosomy
Robertsonian translocation
Tetrasomy
Trisomy
Uniparental disomy
Colcemid
Fragile sites
Germ plasm
Homologous chromosome
Pseudoautosomal region
Synapsis
X chromosome
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Genetic disorders
(34)
Trisomy 13
Trisomy 18
Trisomy 9
4p- syndrome
Distal Trisomy 10q
Distal Trisomy 10q
5p- syndrome
Polydactyly
Karyotype 47,XXX
Mongolism
49 xxxxx syndrome
Microphthalmia
MGA type II
Trisomy 16
Warkany syndrome 2
Trisomy 22
18p deletion syndrome
Karyotype 47,XYY
Microcephaly
Trichorhin- ophalangeal syndrome
1p36 deletion syndrome
Charcot-Marie Tooth Disease
5-oxoprolinuria
4-hydroxybutyric aciduria
Thymic aplasia
49 xxxxy syndrome
Philadelphia chromosome
Jacobsen syndrome
Prader Willi syndrome
Turner syndrome
Hereditary disorder
Trisomy
Monosomy
Chromosome disorders
Tetrasomy
more...
Medical condition
(45)
Chromosome 11 partial trisomy 11q
Chromosome 6 partial trisomy 6q
Chromosome 4 partial trisomy distal 4q
Chromosome 5 trisomy 5p
Chromosome 10 distal trisomy 10q
Chromosome 10 distal trisomy 10q
Chromosome 9 trisomy
18p syndrome
Chromosome 7 partial monosomy 7p
Polyglucosan body disease adult
Congenital hypomyelination
Chromosome 9 trisomy 9p
Chromosome 4 trisomy 4p
Chromosome 3 trisomy 3q2
Chromosome 9 tetrasomy 9p
Chromosome 15 distal trisomy 15q
Camptomelic syndrome
3-M Syndrome
Mental retardation
Chromosome 10 monosomy 10p
Trisomy 13/18
Iris coloboma
Cat eye syndrome
Craniosynostosis
Chromosome 13q deletion
Trigonocephaly
Essential thrombocytopenia
Trisomy 13
Trisomy 18
Trisomy 9
5p- syndrome
Polydactyly
Karyotype 47,XXX
Mongolism
Chromosome disorders
Microphthalmia
MGA type II
Karyotype 47,XYY
Microcephaly
Trichorhin- ophalangeal syndrome
Charcot-Marie Tooth Disease
Thymic aplasia
49 xxxxy syndrome
Jacobsen syndrome
Prader Willi syndrome
Uniparental disomy
more...
Syndromes
(15)
Trisomy 13
Trisomy 18
4p- syndrome
Distal Trisomy 10q
5p- syndrome
5p- syndrome
Karyotype 47,XXX
Mongolism
Warkany syndrome 2
18p deletion syndrome
3-M Syndrome
Karyotype 47,XYY
Thymic aplasia
49 xxxxy syndrome
Prader Willi syndrome
Turner syndrome
more...
Genetics
Chromosomes
Mosaicism
Introduction to genetics
Non-disjunction
Cytogenetic
Karyotype 47,XYY
Hereditary disorder
Genetic disorder
Trisomy 9
Trisomy 16
Warkany syndrome 2
Trisomy 22
Trichorhin- ophalangeal syndrome
Congenital disorders
Congenital anomaly
Holoprosencephaly
Polydactyly
18p deletion syndrome
Microcephaly
Cat eye syndrome
Trigonocephaly
Chromosomes
(54)
Chromosome 11
Chromosome 13
Chromosome 15
Chromosome 18
Chromosome 21
Chromosome 21
Chromosome 3
Chromosome 4
Chromosome 5
Chromosome 7
Isochromosome
Marker chromosome
Pericentric inversion
Ring chromosome
Short arm
Subtelomere
AZF1
Allosome
Autosomal
Centromere
Chromatid
Chromomere
Chromosomal translocation
Chromosome
Chromosome 1 (human)
Chromosome 10 (human)
Chromosome 12 (human)
Chromosome 14 (human)
Chromosome 16 (human)
Chromosome 17 (human)
Chromosome 19 (human)
Chromosome 2 (human)
Chromosome 20 (human)
Chromosome 22 (human)
Chromosome 8 (human)
Chromosome 9 (human)
Chromosome conformation capture
Chromosome disorders
Chromosome regions
Chromosome segregation
Derivative chromosome
Dicentric chromosome
Dyad (biology)
G banding
Human β-globin locus
Inchrosil
Karyotype
Lampbrush chromosome
Proline-Rich Coiled Coil 1
Satellite chromosome
Small supernumerary marker chromosome
Syntelic
Telomere
X chromosome
Y chromosome
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See also
(20)
Diseases and disorders
Am. J. Med. Genet.
Trisomy 21
Craniofacial
Prenatal diagnosis
Prenatal diagnosis
The Long Arm
Distal
Genetic counseling
6Q
Polyploidy
XXYY syndrome
March of Dimes Birth Defects Foundation
Brushfield spots
Growth retardation
Maternal age
13Q
Array CGH
Telecanthus
Hypoplastic
Hypotelorism
more...
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