Multiple congenital anomaly caused by an extra autosome.
about
Camptodactyly, cleft palate, and club foot. A syndrome showing the autosomal-dominant pattern of inheritanceThe William Allan Memorial Award address: human population cytogenetics: the first twenty-five yearsUnisexual and heterosexual meiotic reproduction generate aneuploidy and phenotypic diversity de novo in the yeast Cryptococcus neoformansHistory and evolution of cytogeneticsPROFOUND CHILDHOOD DEAFNESS.Unusual trend in the prevalence of trisomy 13 in mothers aged 35 and older: A population based study of national congenital anomaly data.Non-invasive prenatal detection of trisomy 13 using a single nucleotide polymorphism- and informatics-based approach.Trisomy 13 and extended survival.Clinical experience with trisomies 18 and 13.13-15 trisomy mosiacism in a normal-looking 14-year-old retarded girlFamilial translocation with partial trisomy of 13 and 22: evidence that specific regions of chromosomes 13 and 22 are responsible for the phenotype of each trisomyDevelopmental epigenetics of the murine secondary palateRieger's syndrome with pericentric inversion of chromosome 6.Syndrome of polydactyly, cleft lip/palate or lingual lump, and psychomotor retardation in endogamic gypsies.Four cases of trisomy 18 syndrome with limb reduction malformationsMedical genetics and genomic medicine in the United States of America. Part 1: history, demographics, legislation, and burden of disease.Preaxial polydactyly of the foot: variable expression of trisomy 13 in a case from central Africa.Chromosomal abnormalities associated with cyclopia and synophthalmia.Gestational, perinatal and family findings of patients with Patau syndrome.The locus for Meckel syndrome with multiple congenital anomalies maps to chromosome 17q21-q24.THREE CASES OF TRISOMY IN THE MOUSECharacteristics of highly polymorphic segmental copy-number variations observed in Japanese by BAC-array-CGHAutosomal trisomy syndromes: a detailed study of 27 cases of Edwards' syndrome and 27 cases of Patau's syndrome.Multiple anomalies associated with a small extra metacentric autosome.Chromosome 15 abnormality in a mentally retarded adult.Trisomy 13 syndrome in Chinese infants. Clinical findings and incidence[Ocular manifestations in diseases caused by aberrations in non-sexual chromosomes]Uveal coloboma and true Klinefelter syndrome.Trisomy E and T-E fistula.A partial D-trisomy-normal mosaic femaleA case of partial 14 trisomy 47,XY,(14q-)+ and translocation t(9p+;14q-) in mother and brotherLongevity and Patau syndrome: what determines survival?Differenial chromosome staining.Overexpression of esterase D in kidney from trisomy 13 fetuses.A familial minute isochromosome.Localization of genes on chromosome 13: analysis of two kindreds.CHROMOSOMAL ABNORMALITIES AND ORAL ANOMALIES.Etiology of leukaemias, with special reference to genetic problems.Multiple developmental anomalies and trisomy of a 13-15 group chromosome ('D' syndrome).The XXXXY sex chromosome abnormality
P2860
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P2860
Multiple congenital anomaly caused by an extra autosome.
description
1960 nî lūn-bûn
@nan
1960 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
1960 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
1960年の論文
@ja
1960年論文
@yue
1960年論文
@zh-hant
1960年論文
@zh-hk
1960年論文
@zh-mo
1960年論文
@zh-tw
1960年论文
@wuu
name
Multiple congenital anomaly caused by an extra autosome.
@ast
Multiple congenital anomaly caused by an extra autosome.
@en
Multiple congenital anomaly caused by an extra autosome.
@nl
type
label
Multiple congenital anomaly caused by an extra autosome.
@ast
Multiple congenital anomaly caused by an extra autosome.
@en
Multiple congenital anomaly caused by an extra autosome.
@nl
prefLabel
Multiple congenital anomaly caused by an extra autosome.
@ast
Multiple congenital anomaly caused by an extra autosome.
@en
Multiple congenital anomaly caused by an extra autosome.
@nl
P2093
P1433
P1476
Multiple congenital anomaly caused by an extra autosome.
@en
P2093
P304
P356
10.1016/S0140-6736(60)90676-0
P407
P577
1960-04-01T00:00:00Z