(Q35551173)

8 August 2017

title

Isolation of chromosome-21-specific DNA probes and their use in the analysis of nondisjunction in Down syndrome (English)

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8 August 2017

Galt J

1

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8 August 2017

Boyd E

series ordinal

2

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8 August 2017

Connor JM

series ordinal

3

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8 August 2017

Ferguson-Smith MA

series ordinal

4

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8 August 2017

publication date

1 January 1989

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8 August 2017

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8 August 2017

volume

81

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8 August 2017

issue

2

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8 August 2017

page(s)

113-119

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Human chromosome-specific DNA libraries: use of an oligodeoxynucleotide probe to detect non-recombinants

8 August 2017

cites work

1 reference

12 December 2020

A human X-linked antigen defined by a monoclonal antibody

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12 December 2020

Expression of chromosome 21 specific sequences in normal and Down's syndrome tissues

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12 December 2020

Partial deletion 21: case report with biochemical studies and review

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12 December 2020

Origin of nondisjunction in trisomy 21 syndrome: all studies compiled, parental age analysis, and international comparisons.

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12 December 2020

Regional localization of DNA sequences on chromosome 21 using somatic cell hybrids

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12 December 2020

Regional assignment of human liver-type 6-phosphofructokinase to chromosome 21q22.3 by using somatic cell hybrids and a monoclonal anti-L antibody

1 reference

12 December 2020

Reduced recombination rate on chromosomes 21 that have undergone nondisjunction

1 reference

12 December 2020

The use of DNA probes to establish parental origin in Down syndrome

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12 December 2020

The genetic defect causing familial Alzheimer's disease maps on chromosome 21.

1 reference

12 December 2020

A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity

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12 December 2020

Deletion of a DNA sequence in eight of nine families with X-linked ichthyosis (steroid sulphatase deficiency).

1 reference

12 December 2020

Use of a chromosome 21 cloned DNA probe for the analysis of non-disjunction in Down syndrome

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12 December 2020

Identification of human chromosomes by DNA-binding fluorescent agents

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12 December 2020

Non-disjunction in trisomy 21: study of chromosomal heteromorphisms in 110 families

1 reference

12 December 2020

Complementation Patterns of Thy-1 Variants and Evidence That Antigen Loss Variants “Pre-Exist” in the Parental Population 2

1 reference

12 December 2020

Down syndrome and maternal age: the effect of erroneous assignment of parental origin

1 reference

12 December 2020

Human gene mapping 9. Paris conference (1987). Ninth International Workshop on Human Gene Mapping

1 reference

12 December 2020

Isolation and regional mapping of DNA sequences unique to human chromosome 21.

1 reference

12 December 2020

Parental alpha 1-antitrypsin (PI) types and meiotic nondisjunction in the aetiology of Down syndrome.

1 reference

12 December 2020

Cloned DNA probes regionally mapped to human chromosome 21 and their use in determining the origin of nondisjunction

1 reference

12 December 2020

Trisomy 21 (Down syndrome): studying nondisjunction and meiotic recombination by using cytogenetic and molecular polymorphisms that span chromosome 21.

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12 December 2020

Report of the committee on human gene mapping by recombinant DNA techniques

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12 December 2020

Construction of fifteen human chromosome-specific DNA libraries from flow-purified chromosomes

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12 December 2020

Molecular analysis of chromosome 21 using somatic cell hybrids

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12 December 2020

Cytogenetic and molecular studies of trisomy 13.

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12 December 2020

Identifiers

DOI

10.1007/BF00293885

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8 August 2017

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