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 yearsHistory and evolution of cytogeneticsClinical experience with trisomies 18 and 13.Identification of group'E' chromosome abnormalities in human cells.Oesophageal atresia in the South West of England.Intraocular pathology of trisomy 18 (Edwards's syndrome): report of a case and review of the literature.Rieger's syndrome with pericentric inversion of chromosome 6.Four cases of trisomy 18 syndrome with limb reduction malformationsCraniofacial abnormalities among patients with Edwards Syndrome.The trisomy 18 syndrome.Autosomal trisomy syndromes: a detailed study of 27 cases of Edwards' syndrome and 27 cases of Patau's syndrome.An extra small metacentric chromosome in a mentally retarded boyMultiple anomalies associated with a small extra metacentric autosome.Trisomy 18 syndrome in Chinese infants. Clinical findings and incidence.Double autosomal trisomy and mosaicism for three cell lines in man: coexisting trisomy 13-15, trisomy 17-18, and a minority cell line trisomic for a chromosome of both groupsTrisomy 18 mosaicism: report of two cases.[Ocular manifestations in diseases caused by aberrations in non-sexual chromosomes]Trisomy E and T-E fistula.Trisomy E (18) syndrome: clinical spectrum in 12 new cases, including chromosome autoradiography in 4.Gene deletion and duplication effects on phenotype and gamma globulin levelsTrisomy-18 syndrome caused by translocation or isochromosome formation. A case report with bibliography.Trisomy 18 in one of fraternal twinsMolecular studies of trisomy 18Frequency and occurrence of chromosomal syndromes: II. E-trisomy.A familial minute isochromosome.Survival and the sex ratio in trisomy 17-18CHROMOSOMAL ABNORMALITIES AND ORAL ANOMALIES.Transcriptomic analysis of cell-free fetal RNA suggests a specific molecular phenotype in trisomy 18.A Search for Ocular Anomalies in Persons with Abnormal Numbers of Sex Chromosomes.Expanding diagnostic testing beyond cytogenetics: implications for birth defects research and surveillanceA familial chromosome translocation associated with speech and mental retardation.The D triisomy syndrome and XO gonadal dysgenesis in two sisters.Cytogenetics: past, present and future.PROBABLE DELETION OF THE SHORT ARM OF CHROMOSOME 18.E (16-18) trisomy syndrome: analysis of 13 casesSimultaneous discovery and testing of deletions for disease association in SNP genotyping studies.Strategies for the detection of copy number and other structural variants in the human genome.Chromosome studies in man: past achievements and recent advancesClinical features and survival in individuals with trisomy 18: A retrospective one-center study of 44 patients who received intensive care treatments
P2860
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P2860
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
A new trisomic syndrome.
@ast
A new trisomic syndrome.
@en
type
label
A new trisomic syndrome.
@ast
A new trisomic syndrome.
@en
prefLabel
A new trisomic syndrome.
@ast
A new trisomic syndrome.
@en
P2093
P1433
P1476
A new trisomic syndrome.
@en
P2093
A H CAMERON
D G HARNDEN
J H EDWARDS
V M CROSSE
P304
P356
10.1016/S0140-6736(60)90675-9
P407
P577
1960-04-01T00:00:00Z