(Q33585835)

28 July 2017

Fluorescence and autoradiographic studies in patients with Turner's syndrome and 46,XXp- and 46,XXq- karyotypes (English)

1 reference

28 July 2017

0 references

Boczkowski K

1

1 reference

PubMed ID

4129970

28 July 2017

Mikkelsen M

series ordinal

2

1 reference

PubMed ID

4129970

28 July 2017

language of work or name

English

0 references

publication date

1 December 1973

1 reference

Journal of Medical Genetics

28 July 2017

1 reference

28 July 2017

10

1 reference

28 July 2017

350-355

1 reference

28 July 2017

4

1 reference

KARYOTYPE-PHENOTYPE CORRELATIONS IN GONADAL DYSGENESIS AND THEIR BEARING ON THE PATHOGENESIS OF MALFORMATIONS

28 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013055

Evidence that the Xg blood group genes are on the short arm of the X chromosome

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013055

Chromosome preparations of leukocytes cultured from human peripheral blood

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013055

Gene action in the X-chromosome of the mouse (Mus musculus L.)

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013055

Apparent deletion of X chromosome in a prepuberal girl

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013055

Somatic stigmata of Turner's syndrome in a patient with 46,XXq-

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013055

Structural abnormalities of the sex chromosomes

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013055

Evidence that the Xg locus is inactivated in structurally abnormal X chromosomes

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013055

Identification of human chromosomes by DNA-binding fluorescent agents

31 October 2018

1 reference

12 December 2020

Internal asynchrony in late replication of human X chromosomes with structural abnormalities

1 reference

12 December 2020

X g and X chromosome inactivation

1 reference

12 December 2020

An inhertited X‐autosome translocation in man

1 reference

12 December 2020

Identifiers

PMCID

1013055

1 reference

28 July 2017

1 reference

PubMed ID

4129970