(Q35197231)

7 August 2017

title

Prenatal diagnosis and carrier detection of a cryptic translocation by using DNA markers from the short arm of chromosome 5 (English)

1 reference

7 August 2017

J Overhauser

1

1 reference

7 August 2017

U Bengtsson

2

1 reference

7 August 2017

J McMahon

3

1 reference

7 August 2017

J Ulm

4

1 reference

7 August 2017

M G Butler

5

1 reference

7 August 2017

L Santiago

6

1 reference

7 August 2017

J J Wasmuth

7

1 reference

7 August 2017

language of work or name

English

0 references

publication date

1 August 1989

1 reference

American Journal of Human Genetics

7 August 2017

published in

1 reference

7 August 2017

volume

45

1 reference

7 August 2017

issue

2

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7 August 2017

page(s)

296-303

1 reference

Selective linkage disruption in human-Chinese hamster cell hybrids: deletion mapping of the leuS, hexB, emtB, and chr genes on human chromosome 5

7 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683354

Expression of recessive alleles by chromosomal mechanisms in retinoblastoma

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683354

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

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683354

Molecular analysis of an unbalanced deletion of the short arm of chromosome 5 that produces no phenotype

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683354

Molecular detection of microscopic and submicroscopic deletions associated with Miller-Dieker syndrome

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683354

Detection of submicroscopic deletions in band 17p13 in patients with the Miller-Dieker syndrome.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683354

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

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683354

Identification of 28 DNA fragments that detect RFLPs in 13 distinct physical regions of the short arm of chromosome 5.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683354

A fine structure physical map of the short arm of chromosome 5

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683354

The Cri du Chat syndrome: epidemiology, cytogenetics, and clinical features

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683354

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

13 July 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/2667351

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

PMC publication ID

1683354

1 reference

7 August 2017

1 reference