(Q69134747)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3610150%20AND%20SRC:MED&resulttype=core&format=json

29 September 2019

title

Chromosome deletion at 11q23 in an abnormal child from a family with inherited fragility at 11q23 (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3610150%20AND%20SRC:MED&resulttype=core&format=json

29 September 2019

author name string

L E Voullaire

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3610150%20AND%20SRC:MED&resulttype=core&format=json

29 September 2019

G C Webb

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3610150%20AND%20SRC:MED&resulttype=core&format=json

29 September 2019

M A Leversha

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3610150%20AND%20SRC:MED&resulttype=core&format=json

29 September 2019

publication date

1 June 1987

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3610150%20AND%20SRC:MED&resulttype=core&format=json

29 September 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3610150%20AND%20SRC:MED&resulttype=core&format=json

29 September 2019

volume

76

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3610150%20AND%20SRC:MED&resulttype=core&format=json

29 September 2019

issue

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3610150%20AND%20SRC:MED&resulttype=core&format=json

29 September 2019

page(s)

202-204

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3610150%20AND%20SRC:MED&resulttype=core&format=json

Spontaneous expression of fra(11)(q23) in a patient with Ewing's sarcoma and t(11;22)(q23;q11)

29 September 2019

cites work

1 reference

12 December 2020

Partial deletion of long arm of chromosome 11[del(11)(q23)]: Jacobsen syndrome. Two new cases and review of the clinical findings

1 reference

12 December 2020

Familial fragile site found at the cancer breakpoint (1)(q32). Inducibility by distamycin A, concomitance with fragile (16)(q22)

1 reference

12 December 2020

Clinical and hematologic characteristics in acute leukemia with 11q23 translocations

1 reference

12 December 2020

Partial 11q monosomy and trigonocephaly. A new syndrome

1 reference

12 December 2020

Fragile sites and chromosome breakpoints in constitutional rearrangements II. Spontaneous abortions, stillbirths and newborns

1 reference

12 December 2020

Fragile sites and structural rearrangements in cancer

1 reference

12 December 2020

Fragile sites and chromosome breakpoints in constitutional rearrangements I. Amniocentesis

1 reference

12 December 2020

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

1 reference

12 December 2020

Partial monosomy due to long-arm deletion of chromosome 11 : del (11) (q23) (author's transl)

1 reference

12 December 2020