(Q33586317)

28 July 2017

Karyotype 45,XX,-21/46,XX,21q-in an infant with symptoms of G-deletion syndrome I (English)

1 reference

28 July 2017

0 references

Mikkelsen M

1

1 reference

PubMed ID

4140913

28 July 2017

Vestermark S

series ordinal

2

1 reference

PubMed ID

4140913

28 July 2017

language of work or name

English

0 references

publication date

1 December 1974

1 reference

Journal of Medical Genetics

28 July 2017

1 reference

28 July 2017

11

1 reference

28 July 2017

389-393

1 reference

28 July 2017

4

1 reference

Apparent monosomy of a G autosome in a Jamaican infant

28 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013215

Monosomy G: case report and review of the literature

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013215

Monosomy for the centromeric regions of chromosome 21

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013215

A 45,XX,21--child: attempt at a cytological and clinical interpretation of the karyotype

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013215

Probable monosomy-21 and partial trisomy.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013215

A "G" deletion syndrome anti-mongolism

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013215

22-ring chromosome: identification by controlled heat denaturation

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013215

Identification by fluorescent microscopy of the abnormal chromosomes associated with the G-deletion syndromes

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013215

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013215

A Child With Partial Deletion of a G-Group Autosome

31 October 2018

1 reference

12 December 2020

Autosomal monosomy in man. Complete monosomy G (21-22) in a four-and-one-half-year-old mentally retarded girl

1 reference

12 December 2020

A case of monosomy G?

1 reference

12 December 2020

Identification of human chromosomes by DNA-binding fluorescent agents

1 reference

12 December 2020

[Viability in monosomy G]

1 reference

12 December 2020

The G deletion syndromes

1 reference

12 December 2020

Identification of 21 r and 22r chromosomes by quinacrine fluorescence

1 reference

12 December 2020

Identification by fluorescence of two G rings: (46,XY,21r) G deletion syndrome I and (46, XX, 22r) G deletion syndrome II

1 reference

12 December 2020

(6;15) Translocation with loss of chromosome material in the patient and various chromosome aberrations in family members

1 reference

12 December 2020

A child with a 21-ring chromosome, 45XX,21minus-46,XX,21r investigated with the banding technique

1 reference

12 December 2020

[PARTIAL MONOSOMY FOR A SMALL ACROCENTRIC CHROMOSOME.]

1 reference

12 December 2020

Identifiers

PMCID

1013215

1 reference

28 July 2017

1 reference

PubMed ID

4140913