(Q55059766)

English

Pure partial trisomy of the short arm of chromosome 5.

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

16 June 2018

http://europepmc.org/abstract/MED/2731942

Pure partial trisomy of the short arm of chromosome 5. (English)

1 reference

Europe PubMed Central

PubMed publication ID

16 June 2018

http://europepmc.org/abstract/MED/2731942

author name string

M O Rethoré

1

1 reference

Europe PubMed Central

PubMed publication ID

16 June 2018

http://europepmc.org/abstract/MED/2731942

M C Blois

2

1 reference

Europe PubMed Central

PubMed publication ID

16 June 2018

http://europepmc.org/abstract/MED/2731942

M Peeters

3

1 reference

Europe PubMed Central

PubMed publication ID

16 June 2018

http://europepmc.org/abstract/MED/2731942

P Popowski

4

1 reference

Europe PubMed Central

PubMed publication ID

16 June 2018

http://europepmc.org/abstract/MED/2731942

C Pangalos

5

1 reference

Europe PubMed Central

PubMed publication ID

16 June 2018

http://europepmc.org/abstract/MED/2731942

J Lejeune

6

1 reference

Europe PubMed Central

PubMed publication ID

16 June 2018

http://europepmc.org/abstract/MED/2731942

publication date

1 June 1989

1 reference

Europe PubMed Central

PubMed publication ID

16 June 2018

http://europepmc.org/abstract/MED/2731942

1 reference

Europe PubMed Central

PubMed publication ID

16 June 2018

http://europepmc.org/abstract/MED/2731942

82

1 reference

Europe PubMed Central

PubMed publication ID

16 June 2018

http://europepmc.org/abstract/MED/2731942

3

1 reference

Europe PubMed Central

PubMed publication ID

16 June 2018

http://europepmc.org/abstract/MED/2731942

296-298

1 reference

Europe PubMed Central

PubMed publication ID

16 June 2018

http://europepmc.org/abstract/MED/2731942

https://scigraph.springernature.com/pub.10.1007/bf00291177

0 references

Familial partial trisomy 5p resulting from segregation of an insertional translocation

1 reference

https://pubmed.ncbi.nlm.nih.gov/2731942

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A clinical syndrome associated with dup(5p)

1 reference

https://pubmed.ncbi.nlm.nih.gov/2731942

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A case report of a de novo tandem duplication (5p) (p14----pter)

1 reference

https://pubmed.ncbi.nlm.nih.gov/2731942

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

"Complete" trisomy 5p; de novo translocation t(2;5)(q36;p11) with isochromosome 5p. Case report and review of the literature

1 reference

https://pubmed.ncbi.nlm.nih.gov/2731942

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Presumptive direct insertion within chromosome 2 in man

1 reference

https://pubmed.ncbi.nlm.nih.gov/2731942

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

On two familial cases of complex translocations

1 reference

https://pubmed.ncbi.nlm.nih.gov/2731942

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Interstitial 3p deletion in a child due to paternal paracentric inserted inversion

1 reference

https://pubmed.ncbi.nlm.nih.gov/2731942

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A 4-5/21-22 CHROMOSOMAL TRANSLOCATION ASSOCIATED WITH MULTIPLE CONGENITAL ANOMALIES

1 reference

https://pubmed.ncbi.nlm.nih.gov/2731942

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

FAMILIAL SEGREGATION OF A 5-13 TRANSLOCATION DETERMINING PARTIAL MONOSOMY AND A TRISOMY OF THE SHORT ARM OF THE 5 CHROMOSOME: "CAT CRY" DISEASE AND ITS "RECEPROCAL"

1 reference

https://pubmed.ncbi.nlm.nih.gov/2731942

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Duplication 5q(5q22----5q33): from an intrachromosomal insertion

1 reference

https://pubmed.ncbi.nlm.nih.gov/2731942

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Trisomy of the short arm of chromosome 5: autopsy data in a malformed newborn with inv dup (5) (p13.1----p15.3).

1 reference

https://pubmed.ncbi.nlm.nih.gov/2731942

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Partial trisomy 1 due to a "shift" and probable location of the Duffy (Fy) locus

1 reference

https://pubmed.ncbi.nlm.nih.gov/2731942

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Complete trisomy 5p owing to de novo translocation t(5;22)(q11;p11) with isochromosome 5p associated with a familial pericentric inversion of chromosome 2, inv 2(p21q11)

1 reference

https://pubmed.ncbi.nlm.nih.gov/2731942

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

'Complete 5p' trisomy: 1 case and 19 translocation carriers in 6 generations

1 reference

https://pubmed.ncbi.nlm.nih.gov/2731942

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

3 CASES OF PARTIAL DELETION OF THE SHORT ARM OF A 5 CHROMOSOME

1 reference

https://pubmed.ncbi.nlm.nih.gov/2731942

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identical multiple congenital anomalies/mental retardation (MCA/MR) syndrome due to del(2)(q32) in two sisters with intrachromosomal insertional translocation in their father

1 reference

https://pubmed.ncbi.nlm.nih.gov/2731942

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Duplication of 16p from insertion of 16p into 16q with subsequent duplication due to crossing over within the inserted segment.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2731942

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00291177

1 reference

Europe PubMed Central

PubMed publication ID

16 June 2018

http://europepmc.org/abstract/MED/2731942

Dimensions Publication ID

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

16 June 2018

http://europepmc.org/abstract/MED/2731942

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