(Q70794729)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6540242%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

title

Identical twins with deletion 16q syndrome: evidence that 16q12.2-q13 is the critical band region (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6540242%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

author name string

F F Elder

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6540242%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

J W Ferguson

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6540242%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

L H Lockhart

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6540242%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

publication date

1 January 1984

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6540242%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6540242%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

volume

67

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6540242%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

issue

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6540242%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

page(s)

233-236

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6540242%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1007/bf00273010

13 October 2019

exact match

0 references

cites work

The characterization of high-resolution G-banded chromosomes of man

1 reference

12 December 2020

Interstitial 16q deletion with typical dysmorphic syndrome

1 reference

12 December 2020

An international system for human cytogenetic nomenclature--high-resolution banding (1981). ISCN (1981). Report of the Standing Committee on Human Cytogenetic Nomenclature

1 reference

12 December 2020

A ring chromosome No. 16 in an infant with primary hypoparathyroidism

1 reference

12 December 2020

A terminal long arm deletion of chromosome 16 in a dysmorphic infant: 46,XY,del(16) (q22)

1 reference

12 December 2020

[Chromosome 16 syndromes]

1 reference

12 December 2020

High Resolution of Human Chromosomes

1 reference

12 December 2020

Interstitial deletion for a region in the long arm of chromosome 16

1 reference

12 December 2020

Partial monosomy of the long arm of chromosome 16: A distinct clinical entity?

1 reference

12 December 2020

Partial monosomy of the long arm of chromosome 16 in a malformed newborn: karyotype 46,XX,del(16))q21)

1 reference

12 December 2020

Fryns syndrome without deletion 16q.

1 reference

12 December 2020

Miller-Dieker syndrome: lissencephaly and monosomy 17p.

1 reference

12 December 2020

Langer-Giedion syndrome with and without del 8q. assignment of critical segment to 8q23

1 reference

12 December 2020

A rapid banding technique for human chromosomes

1 reference

12 December 2020

1 reference

12 December 2020

Deficiency, transposition, and duplication of one 15q region may be alternatively associated with Prader-Willi (or a similar) syndrome. Analysis of seven cases after varying ascertainment.

1 reference

12 December 2020

Deletions of chromosome 15 as a cause of the Prader-Willi syndrome

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00273010

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6540242%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

1 reference