(Q57745738)

English

Cryptic subtelomeric translocation t(2;16)(q37;q24) segregating in a family with unexplained stillbirths and a dysmorphic, slightly retarded child

article by Daniela Giardino et al published December 2001 in European Journal of Human Genetics

In more languages

Statements

scholarly article

0 references

Cryptic subtelomeric translocation t(2;16)(q37;q24) segregating in a family with unexplained stillbirths and a dysmorphic, slightly retarded child (English)

0 references

0 references

object named as

Palma Finelli

2

0 references

object named as

Fabio Mosca

5

0 references

author name string

Daniela Giardino

1

0 references

Giulietta Gottardi

3

0 references

Donata Clerici

4

0 references

Vincenza Briscioli

6

0 references

Lidia Larizza

7

0 references

publication date

December 2001

0 references

European Journal of Human Genetics

0 references

9

0 references

12

0 references

881-886

0 references

https://scigraph.springernature.com/pub.10.1038/sj.ejhg.5200730

0 references

Subtle chromosomal rearrangements in children with unexplained mental retardation

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200730

7 January 2021

based on heuristic

inferred from DOI database lookup

Perfect endings: a review of subtelomeric probes and their use in clinical diagnosis

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200730

7 January 2021

based on heuristic

inferred from DOI database lookup

Molecular-cytogenetic detection of a deletion of 1p36.3.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200730

7 January 2021

based on heuristic

inferred from DOI database lookup

The detection of subtelomeric chromosomal rearrangements in idiopathic mental retardation

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200730

7 January 2021

based on heuristic

inferred from DOI database lookup

High resolution chromosome analysis and in situ hybridization on amniotic fluid for diagnosis of a cryptic translocation

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200730

7 January 2021

based on heuristic

inferred from DOI database lookup

Albright hereditary osteodystrophy and del(2)(q37.3) in four unrelated individuals

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200730

7 January 2021

based on heuristic

inferred from DOI database lookup

RDCI, the vasoactive intestinal peptide receptor: a candidate gene for the features of Albright hereditary osteodystrophy associated with deletion of 2q37

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200730

7 January 2021

based on heuristic

inferred from DOI database lookup

Inverted duplications are recurrent rearrangements always associated with a distal deletion: description of a new case involving 2q

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200730

7 January 2021

based on heuristic

inferred from DOI database lookup

Trisomy 16q23----qter arising from a maternal t(13;16)(p12;q23): case report and evidence of the reciprocal balanced maternal rearrangement by the Ag-NOR technique

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200730

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1038/SJ.EJHG.5200730

0 references

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q57745738&oldid=1827136991"