about
Neurocognitive outcomes of individuals with a sex chromosome trisomy: XXX, XYY, or XXY: a systematic reviewPrenatal and postnatal prevalence of Turner's syndrome: a registry studyThe William Allan Memorial Award address: human population cytogenetics: the first twenty-five yearsChildren with sex chromosome trisomies: parental disclosure of genetic status.Trisomy 18 syndrome with an unusual karyotype: possible double isochromosome.Familial mental retardation in a family with an inherited chromosome rearrangement.Reciprocal translocations in man. 3:1 Meiotic disjunction resulting in 47- or 45-chromosome offspring.Prenatal diagnosis of genetic disordersChromosome survey of total population of mentally subnormal in North-East of ScotlandPartial monosomy and partial trisomy 18 in two offspring of carrier of pericentric inversion of chromosome 18.Colchester revisited: a genetic study of mental defect.Chromosome anomalies among livebirthsChromosome survey of total population of mentally subnormal in North-East Scotland.Dissociation as probable origin of mosaic 45,XY,t(15;21)/46,XY,i(21q)Pericentric inversions inv(2)(p11q13) and inv(2)(p13q11) in 2 unrelated families.Prenatal diagnosis of a de novo Y/22 translocationClinical manifestations of familial 13;18 translocation.Trisomy 14 mosaicism in a translocation 14q15q carrier: probable dissociation and isochromosome formationInheritance of a ring 14 chromosomeBalanced rearrangements of the autosomes: results of a longitudinal study of a newborn survey population.A familial insertion involving an active nucleolar organiser within chromosome 12Small extra ring chromosome derived from chromosome 10p: clinical report and characterisation by FISH.47,XXY (Klinefelter syndrome) and 47,XYY: estimated rates of and indication for postnatal diagnosis with implications for prenatal counselling.Embryos of robertsonian translocation carriers exhibit a mitotic interchromosomal effect that enhances genetic instability during early developmentSex chromosome trisomies in Europe: prevalence, prenatal detection and outcome of pregnancyAspects of the treatment of Turner syndrome.Is the prevalence of Klinefelter syndrome increasing?Pericentric inversion of chromosome 18 in parents leading to a phenotypically normal child with segmental uniparental disomy 18.Meiotic nondisjunction in the mouse: methodology for genetic testing and comparison with other methodsTesting for nondisjunction in the mouseDe novo microdeletion on an inherited Robertsonian translocation chromosome: a cause for dysmorphism in the apparently balanced translocation carrier.Identification of DNA sequences flanking the breakpoint of human t(14q21q) Robertsonian translocations.Comparative mapping of the constitutional and tumor-associated 11;22 translocations.Mutation rates of structural chromosome rearrangements in man.Human population cytogenetics: dilemmas and problems.The frequency of chromosome aberrations in tall men with special reference to 47, XYY and 47, XXY.Acrocentric chromosome associations in man.Mental retardation associated with "balanced" chromosome rearrangements.Maternal-age effect in aneuploidy: does altered embryonic selection play a role?The frequency and mutation rate of balanced autosomal rearrangements in man estimated from prenatal genetic studies for advanced maternal age
P2860
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P2860
description
1974 nî lūn-bûn
@nan
1974 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
1974 թվականի մայիսին հրատարակված գիտական հոդված
@hy
1974年の論文
@ja
1974年学术文章
@wuu
1974年学术文章
@zh-cn
1974年学术文章
@zh-hans
1974年学术文章
@zh-my
1974年学术文章
@zh-sg
1974年學術文章
@yue
name
A cytogenetic survey of 11,680 newborn infants.
@ast
A cytogenetic survey of 11,680 newborn infants.
@en
A cytogenetic survey of 11,680 newborn infants.
@nl
type
label
A cytogenetic survey of 11,680 newborn infants.
@ast
A cytogenetic survey of 11,680 newborn infants.
@en
A cytogenetic survey of 11,680 newborn infants.
@nl
prefLabel
A cytogenetic survey of 11,680 newborn infants.
@ast
A cytogenetic survey of 11,680 newborn infants.
@en
A cytogenetic survey of 11,680 newborn infants.
@nl
P2093
P2860
P1476
A cytogenetic survey of 11,680 newborn infants.
@en
P2093
P2860
P304
P356
10.1111/J.1469-1809.1974.TB01843.X
P407
P577
1974-05-01T00:00:00Z