(Q39903975)

English

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

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

15 September 2017

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

1 reference

Europe PubMed Central

PubMed publication ID

15 September 2017

1 reference

based on heuristic

inferred from title

author name string

N J Leschot

1

1 reference

Europe PubMed Central

PubMed publication ID

15 September 2017

K S Lim

2

1 reference

Europe PubMed Central

PubMed publication ID

15 September 2017

publication date

1 February 1979

1 reference

Europe PubMed Central

PubMed publication ID

15 September 2017

1 reference

Europe PubMed Central

PubMed publication ID

15 September 2017

46

1 reference

Europe PubMed Central

PubMed publication ID

15 September 2017

3

1 reference

Europe PubMed Central

PubMed publication ID

15 September 2017

271-278

1 reference

Europe PubMed Central

PubMed publication ID

15 September 2017

https://scigraph.springernature.com/pub.10.1007/bf00273310

0 references

Segregation of a balanced translocation t(5p-;Gp+)

1 reference

https://pubmed.ncbi.nlm.nih.gov/437770

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic and clinical study of a family of 7 children in which 3 persons have "crying cat syndrome"

1 reference

https://pubmed.ncbi.nlm.nih.gov/437770

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A partial trisomy 5p syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/437770

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Trisomy 5: delineation of clinical features

1 reference

https://pubmed.ncbi.nlm.nih.gov/437770

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Reverse type of cri du chat disease: 5 p trisomy

1 reference

https://pubmed.ncbi.nlm.nih.gov/437770

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial segregation of a t(5p-;13q+). Complementary analysis from specimens preserved in liquid nitrogen

1 reference

https://pubmed.ncbi.nlm.nih.gov/437770

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Translocation heterozygosis: a cause of five cases of the cri du chat syndrome and two cases with a duplication of chromosome number five in three families

1 reference

https://pubmed.ncbi.nlm.nih.gov/437770

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/437770

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/437770

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of 2 familial translocations

1 reference

https://pubmed.ncbi.nlm.nih.gov/437770

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Partial trisomy for short and long arm of chromosome no. 5: Two cases of two possible syndromes

1 reference

https://pubmed.ncbi.nlm.nih.gov/437770

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Karyotype with chromosomal abnormality with various inherited defects in the offspring (Recombination aneusomy)

1 reference

https://pubmed.ncbi.nlm.nih.gov/437770

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Partial trisomy 5 with a carrier parent t(5p‐;9p+)

1 reference

https://pubmed.ncbi.nlm.nih.gov/437770

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The crying cat syndrome and its reciprocal

1 reference

https://pubmed.ncbi.nlm.nih.gov/437770

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00273310

1 reference

Europe PubMed Central

PubMed publication ID

15 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

15 September 2017

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