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English
Autosomal fragile sites not a current indication for prenatal diagnosis
scientific article published on 01 January 1984
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
6469247
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6469247%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 October 2019
title
Autosomal fragile sites not a current indication for prenatal diagnosis
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
6469247
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6469247%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 October 2019
author
Frederick Hecht
series ordinal
1
object named as
F Hecht
0 references
Barbara K. Hecht
series ordinal
2
object named as
B K Hecht
0 references
publication date
1 January 1984
1 reference
stated in
Europe PubMed Central
PubMed ID
6469247
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6469247%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 October 2019
published in
Human Genetics
1 reference
stated in
Europe PubMed Central
PubMed ID
6469247
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6469247%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 October 2019
volume
67
1 reference
stated in
Europe PubMed Central
PubMed ID
6469247
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6469247%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 October 2019
issue
3
1 reference
stated in
Europe PubMed Central
PubMed ID
6469247
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6469247%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 October 2019
page(s)
352-353
1 reference
stated in
Europe PubMed Central
PubMed ID
6469247
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6469247%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 October 2019
exact match
https://scigraph.springernature.com/pub.10.1007/bf00291370
0 references
cites work
DNA polymerase alpha inhibition by aphidicolin induces gaps and breaks at common fragile sites in human chromosomes
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/6469247
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Heritable Fragile Site on Chromosome 16: Probable Localization of Haptoglobin Locus in Man
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/6469247
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
BrdU-sensitive fragile site on long arm of chromosome 16.
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/6469247
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Demonstration of a heritable fragile site in human chromosome 16 with distamycin A
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/6469247
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Fragile chromosome 16(q22) cause a balanced translocation at the same point
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/6469247
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1007/BF00291370
1 reference
stated in
Europe PubMed Central
PubMed ID
6469247
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6469247%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 October 2019
PubMed ID
6469247
1 reference
stated in
Europe PubMed Central
PubMed ID
6469247
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6469247%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 October 2019
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