(Q35414016)

English

THE XXXXY SYNDROME. A REPORT OF A CASE AND REVIEW OF THE LITERATURE.

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

THE XXXXY SYNDROME. A REPORT OF A CASE AND REVIEW OF THE LITERATURE. (English)

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

author name string

SCHERZ RG

1

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

ROECKEL IE

2

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

language of work or name

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publication date

1 December 1963

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

The Journal of Pediatrics

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Europe PubMed Central

PubMed publication ID

8 August 2017

63

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

1093-1098

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

A child with 49 chromosomes

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2863%2980189-4

7 January 2021

A family with an XXXXY male, a leukaemic male, and two 21-trisomic mongoloid females

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2863%2980189-4

7 January 2021

A case of XXXXY Klinefelter's syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2863%2980189-4

7 January 2021

A new technic for differential staining of the sex chromatin, and the determination of its incidence in exfoliated vaginal epithelial cells

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2863%2980189-4

7 January 2021

A SIMPLE METHOD FOR MAKING CHROMOSOME SLIDES: PREPARATION FROM SHORT-TERM CULTURES OF PERIPHERAL BLOOD

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2863%2980189-4

7 January 2021

A sex-linked blood group

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2863%2980189-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2863%2980189-4

7 January 2021

The triple-X syndrome. Clinical, pathological, and chromosomal studies in three mentally retarded cases.

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2863%2980189-4

7 January 2021

Identifiers

10.1016/S0022-3476(63)80189-4

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

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