(Q34634360)

English

Comparative clinical studies and X chromosome behaviour in a case of XXXX-XXXXX mosaicism

scientific article

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

Comparative clinical studies and X chromosome behaviour in a case of XXXX-XXXXX mosaicism (English)

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

author name string

Cooke P

1

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

Black JA

2

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

Curtis DJ

3

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

language of work or name

0 references

publication date

1 June 1972

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

Journal of Medical Genetics

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

9

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

2

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

235-238

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

CLINICAL AND CYTOGENETIC STUDIES ON A GROUP OF FEMALES WITH XXX SEX CHROMOSOME COMPLEMENTS.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1469025

7 July 2018

An XXXX sex chromosome complex in two mentally defective females

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1469025

7 July 2018

A female with the 48,XXXX karyotype

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1469025

7 July 2018

A female child with five X chromosomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/5046636

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Feeblemindedness and XXXX karyotype

1 reference

https://pubmed.ncbi.nlm.nih.gov/5046636

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[48, XXXX syndrome in a fourteen year old girl]

1 reference

https://pubmed.ncbi.nlm.nih.gov/5046636

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

48, XXXX syndrome in a six year old child. Abnormal transmission of group Xg

1 reference

https://pubmed.ncbi.nlm.nih.gov/5046636

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

48,XXXX-49,XXXXX mosaic: asynchronies among the late-replicating X chromosomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/5046636

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sex chromatin frequency in buccal mucosal tissue: the normal female population

1 reference

https://pubmed.ncbi.nlm.nih.gov/5046636

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sex chromatin frequency in buccal mucosal tissue: The distribution of single, double and triple sex chromatin bodies

1 reference

https://pubmed.ncbi.nlm.nih.gov/5046636

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sex chromatin survey among mentally retarded children in Japan

1 reference

https://pubmed.ncbi.nlm.nih.gov/5046636

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Buccal smears and sex chromatin

1 reference

https://pubmed.ncbi.nlm.nih.gov/5046636

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A PHENOTYPIC FEMALE WITH 49 CHROMOSOMES, PRESUMABLY XXXXX. A CASE REPORT

1 reference

https://pubmed.ncbi.nlm.nih.gov/5046636

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

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