Chromosome analysis on 930 consecutive newborn children using quinacrine fluorescent banding technique.
about
Estimates of the frequency of chromosome abnormalities detectable in unselected newborns using moderate levels of bandingTwo pericentric inversions of human chromosome 11Balanced rearrangements of the autosomes: results of a longitudinal study of a newborn survey population.Is the prevalence of Klinefelter syndrome increasing?The frequency and mutation rate of balanced autosomal rearrangements in man estimated from prenatal genetic studies for advanced maternal ageFamilial retinoblastoma: segregation of chromosome 13 in four families.Rates of 47, + 13 amd 46 translocation D/13 Patau syndrome in live births and comparison with rates in fetal deaths and at amniocentesis.Incidence of fragile X syndrome by newborn screening for methylated FMR1 DNA.The cognitive phenotype in Klinefelter syndrome: a review of the literature including genetic and hormonal factors.Racial differences in the frequency of Q and C chromosomal heteromorphisms.Frequency of RFA colour polymorphisms of human acrocentric chromosomes in caucasians: interrelationship with QFQ polymorphisms.How much difference does chromosome banding make? Adjustments in prevalence and mutation rates of human structural cytogenetic abnormalities.Human chromosomal heteromorphisms in American blacks. IV. Intensity variation in centromeric regions of chromosomes 3 and 4.
P2860
Q24514966-859B9A61-D2FF-4C4E-B278-C227BEC6534BQ33587850-CE833713-5F9B-40D5-A4BA-68C991C16EBCQ33671061-F4569FB4-AC7D-4C2F-92EB-F93A6B0FBC7DQ34713434-7980552D-58C4-4C24-9E0E-711B86D05B07Q35202668-B3938D35-BC06-42C0-8A3F-DE7822A9236FQ35203655-23221975-F581-4F6E-BE57-2BA048D92687Q35204052-3259C3DA-4E72-45B8-87EB-24E55735FA7FQ37373910-1795625E-29F2-466F-A6CD-99A5BE63C10DQ37656038-A6715E69-F8E2-4505-8CB6-75AABC7B5927Q39450980-254BF8F9-3F6B-4C87-A4D9-76F13EB26D9BQ39469985-7E50ACFB-23AB-4CB8-A207-3EB7E7FF2E95Q45284476-1C05B87E-16F3-4778-9CEC-2A0805610AAFQ53951504-1771F0B6-2318-43D2-B3CB-521EB29AE0E4
P2860
Chromosome analysis on 930 consecutive newborn children using quinacrine fluorescent banding technique.
description
1976 nî lūn-bûn
@nan
1976年の論文
@ja
1976年学术文章
@wuu
1976年学术文章
@zh-cn
1976年学术文章
@zh-hans
1976年学术文章
@zh-my
1976年学术文章
@zh-sg
1976年學術文章
@yue
1976年學術文章
@zh
1976年學術文章
@zh-hant
name
Chromosome analysis on 930 con ...... fluorescent banding technique.
@en
Chromosome analysis on 930 con ...... fluorescent banding technique.
@nl
type
label
Chromosome analysis on 930 con ...... fluorescent banding technique.
@en
Chromosome analysis on 930 con ...... fluorescent banding technique.
@nl
prefLabel
Chromosome analysis on 930 con ...... fluorescent banding technique.
@en
Chromosome analysis on 930 con ...... fluorescent banding technique.
@nl
P2093
P356
P1433
P1476
Chromosome analysis on 930 con ...... fluorescent banding technique.
@en
P2093
D R Newton
L M Sewell
M M Gedeon
P Griffith
P2888
P304
P356
10.1007/BF00270861
P577
1976-03-01T00:00:00Z