(Q71144116)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6654336%20AND%20SRC:MED&resulttype=core&format=json

16 October 2019

title

Fragile chromosome 16(q22) cause a balanced translocation at the same point (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6654336%20AND%20SRC:MED&resulttype=core&format=json

16 October 2019

author name string

J M García-Sagredo

1

1 reference

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16 October 2019

C San Román

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6654336%20AND%20SRC:MED&resulttype=core&format=json

16 October 2019

M E Gallego Gómez

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6654336%20AND%20SRC:MED&resulttype=core&format=json

16 October 2019

G Lledo

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6654336%20AND%20SRC:MED&resulttype=core&format=json

16 October 2019

publication date

1 January 1983

1 reference

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16 October 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6654336%20AND%20SRC:MED&resulttype=core&format=json

16 October 2019

volume

65

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6654336%20AND%20SRC:MED&resulttype=core&format=json

16 October 2019

issue

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6654336%20AND%20SRC:MED&resulttype=core&format=json

16 October 2019

page(s)

211-213

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6654336%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1007/bf00286668

16 October 2019

exact match

0 references

cites work

Abnormal childhood phenotypes associated with the same balanced chromosome rearrangements as in the parents

1 reference

12 December 2020

Double heteroploidy, 46, XY, t(13q14q), +18, in a spontaneous abortus

1 reference

12 December 2020

The fragile site on chromosome 16 (q21q22). Data on four new families

1 reference

12 December 2020

Cytogenetic investigation in 413 couples with spontaneous abortions

1 reference

12 December 2020

A cascade of chromosomal aberrations in three generations: a fragile 16q, an extra fragment and a rearranged 20

1 reference

12 December 2020

Heritable Fragile Site on Chromosome 16: Probable Localization of Haptoglobin Locus in Man

1 reference

12 December 2020

Fragile site long arm chromosome 16

1 reference

12 December 2020

Constitutional chromosomal breakage.

1 reference

12 December 2020

Systematic analysis of 95 reciprocal translocations of autosomes

1 reference

12 December 2020

Deleted chromosome 18 with paternal mosaicism

1 reference

12 December 2020

Correlation between euploid structural chromosome rearrangements and mental subnormality in humans.

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00286668

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6654336%20AND%20SRC:MED&resulttype=core&format=json

16 October 2019

1 reference