Nondisjunction of chromosome 15: origin and recombination
about
The comorbidity of autism with the genomic disorders of chromosome 15q11.2-q13Recombination and maternal age-dependent nondisjunction: molecular studies of trisomy 16Meiotic origin of trisomy in confined placental mosaicism is correlated with presence of fetal uniparental disomy, high levels of trisomy in trophoblast, and increased risk of fetal intrauterine growth restrictionMultipoint estimation of genetic maps for human trisomies with one parent or other partial dataMultipoint genetic mapping with uniparental disomy dataMosaic uniparental disomy in Beckwith-Wiedemann syndrome.Der(22)t(11;22) resulting from a paternal de novo translocation, adjacent 1 segregation, and maternal heterodisomy of chromosome 22.The mechanisms involved in formation of deletions and duplications of 15q11-q13.Molecular screening for proximal 15q abnormalities in a mentally retarded population.First-meiotic-division nondisjunction in human oocytes.Skewed X-chromosome inactivation is common in fetuses or newborns associated with confined placental mosaicism.An analysis of the distribution of hetero- and isodisomic regions of chromosome 7 in five mUPD7 Silver-Russell syndrome probands.Molecular studies of chromosomal mosaicism: relative frequency of chromosome gain or loss and possible role of cell selection.Complete paternal isodisomy for chromosome 8 unmasked by lipoprotein lipase deficiency.Bloom syndrome and maternal uniparental disomy for chromosome 15.Paternal isodisomy for chromosome 7 is compatible with normal growth and development in a patient with congenital chloride diarrhea.Uniparental disomy in Robertsonian translocations: strategies for uniparental disomy testingPatterns of meiotic recombination in human fetal oocytes.Formation of upd(7)mat by trisomic rescue: SNP array typing provides new insights in chromosomal nondisjunction.Human female meiosis: new insights into an error-prone process.Current Enlightenment About Etiology and Pharmacological Treatment of Autism Spectrum Disorder.
P2860
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P2860
Nondisjunction of chromosome 15: origin and recombination
description
1993 nî lūn-bûn
@nan
1993 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
1993 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
1993年の論文
@ja
1993年論文
@yue
1993年論文
@zh-hant
1993年論文
@zh-hk
1993年論文
@zh-mo
1993年論文
@zh-tw
1993年论文
@wuu
name
Nondisjunction of chromosome 15: origin and recombination
@ast
Nondisjunction of chromosome 15: origin and recombination
@en
type
label
Nondisjunction of chromosome 15: origin and recombination
@ast
Nondisjunction of chromosome 15: origin and recombination
@en
prefLabel
Nondisjunction of chromosome 15: origin and recombination
@ast
Nondisjunction of chromosome 15: origin and recombination
@en
P2093
P2860
P1476
Nondisjunction of chromosome 15: origin and recombination
@en
P2093
A A Schinzel
A Mutirangura
D H Ledbetter
F Bernasconi
M A Morris
S Langlois
W P Robinson
P2860
P304
P407
P577
1993-09-01T00:00:00Z