An analysis of the break points of structural rearrangements in man
about
The William Allan Memorial Award. Presented to Patricia A. Jacobs, D.Sc., at the annual meeting of the American Society of Human Genetics, Dallas, October 28-31, 1981De novo balanced chromosome rearrangements and extra marker chromosomes identified at prenatal diagnosis: clinical significance and distribution of breakpointsStructure and inheritance of some heterozygous Robertsonian translocation in man.A family with two translocations and a polymorphism involving chromosome 14.Familial translocation 15-22. A possible cause for abortions in female carriersFamilial mental retardation in a family with an inherited chromosome rearrangement.Specific chromosome aberrations in ataxia telangiectasia.Trisomy 8 restricted to cultured fibroblasts.Segregation of an insertional chromosome rearrangement in 3 generations.Gonadal dysgenesis in a patient with an X;3 translocation: case report and reviewFamilial pericentric inversion 19Translocation (X;6) in a female with Duchenne muscular dystrophy: implications for the localisation of the DMD locusA child with a recombinant of chromosome 8 inherited from her carrier mother.Balanced reciprocal whole arm translocation t(3;9): analysis by fluorescence in situ hybridisation.Familial pericentric inversion inv(8)(p23q11)Mutagen specificity in the induction of chromosomal aberrations in somatic cells of Drosophila melanogaster.Nonrandom distribution of exchange points in patients with structural rearrangements.Genetic risk for recombinant 8 syndrome and the transmission rate of balanced inversion 8 in the Hispanic population of the southwestern United StatesA large pericentric inversion of human chromosome 8Mental retardation associated with "balanced" chromosome rearrangements.Report of large kinship with familial translocation between chromosomes 21 and 22.Higher risk to D;G translocation carriers fo tdic(13;21) as compared to tdic(14;21)Chromosome studies in man: past achievements and recent advancesFunctional implications of differential chromosome banding.Genomic organization of the human asparagine transfer RNA genes: localization to the U1 RNA gene and class I pseudogene repeat units.Familial partial 14 trisomy.
P2860
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P2860
An analysis of the break points of structural rearrangements in man
description
1974 nî lūn-bûn
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1974 թուականի Մարտին հրատարակուած գիտական յօդուած
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1974 թվականի մարտին հրատարակված գիտական հոդված
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1974年の論文
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1974年論文
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1974年論文
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1974年論文
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1974年論文
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1974年論文
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1974年论文
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name
An analysis of the break points of structural rearrangements in man
@ast
An analysis of the break points of structural rearrangements in man
@en
An analysis of the break points of structural rearrangements in man.
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type
label
An analysis of the break points of structural rearrangements in man
@ast
An analysis of the break points of structural rearrangements in man
@en
An analysis of the break points of structural rearrangements in man.
@nl
prefLabel
An analysis of the break points of structural rearrangements in man
@ast
An analysis of the break points of structural rearrangements in man
@en
An analysis of the break points of structural rearrangements in man.
@nl
P2093
P2860
P356
P1476
An analysis of the break points of structural rearrangements in man
@en
P2093
C Cunningham
K E Buckton
P A Jacobs
P2860
P356
10.1136/JMG.11.1.50
P407
P577
1974-03-01T00:00:00Z