TURNER SYNDROME DUE TO PRESUMPTIVE X-ISOCHROMOSOME; REPORT OF A CASE (Q78396338)

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14 December 2019

title

TURNER SYNDROME DUE TO PRESUMPTIVE X-ISOCHROMOSOME; REPORT OF A CASE (English)

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14 December 2019

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R L SUMMITT

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14 December 2019

W T DOBBINS

series ordinal

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14 December 2019

publication date

1 July 1965

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The Journal of Pediatrics

14 December 2019

published in

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14 December 2019

volume

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14 December 2019

page(s)

76-83

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A sex-chromosome anomaly in a case of gonadal dysgenesis (Turner's syndrome).

14 December 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2865%2980306-7

THE SOMATIC CHROMOSOMAL CONSTITUTION OF SOME HUMAN SUBJECTS WITH GENETIC DEFECTS

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2865%2980306-7

Plasma level of growth hormone and chromosome complement in four patients with gonadal dysgenesis (Turner's syndrome)

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2865%2980306-7

Cytogenetic studies in primary amenorrhoea

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2865%2980306-7

Chromosome abnormalities as a cause of human infertility

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2865%2980306-7

Sex-chromosome abnormalities in a population of mentally defective children

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2865%2980306-7

A probable isochromosome in a child with multiple congenital anomalies

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2865%2980306-7

Hashimoto's disease in Turner's syndrome with isochromosome X

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2865%2980306-7

HUMAN SEX CHROMOSOME ABNORMALITIES IN RELATION TO DNA REPLICATION AND HETEROCHROMATINIZATION.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2865%2980306-7

AUTORADIOGRAPHIC STUDIES OF X-CHROMOSOME DUPLICATION IN AN XO-X-ISOCHROMOSOME X MOSAIC HUMAN FEMALE

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2865%2980306-7

The normal human female as a mosaic of X-chromosome activity: studies using the gene for C-6-PD-deficiency as a marker

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2865%2980306-7

The single-X nature of sex chromatin in man

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2865%2980306-7

Asynchronous duplication of human chromosomes and the origin of sex chromatin

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2865%2980306-7

Sex Chromatin Mass in Living, Cultivated Human Cells

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2865%2980306-7

Time-Sequence of Human Chromosome Duplication

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2865%2980306-7

Chromosome preparations of leukocytes cultured from human peripheral blood

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2865%2980306-7

Presumptive iso-chromosomes for the long arm of X in man. Analysis of five families

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2865%2980306-7

The pattern of X-chromosome deoxy-ribonucleic acid synthesis in two women with abnormal sex-chromosome complements

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2865%2980306-7

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2865%2980306-7

Autoimmunity: some aetiological aspects. Inflammatory polyarthritis and rheumatoid arthritis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2865%2980306-7

AUTOIMMUNITY. AETIOLOGICAL ASPECTS OF CHRONIC DISCOID AND SYSTEMIC LUPUS ERYTHEMATOSUS, SYSTEMIC SCLEROSIS, AND HASHIMOTO'S THYROIDITIS: SOME IMMUNOLOGICAL IMPLICATIONS

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2865%2980306-7

Mammalian X-chromosome action: inactivation limited in spread and region of origin

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2865%2980306-7

Misdivision of univalents in common wheat

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2865%2980306-7

7 January 2021

The Chromosomes of Man

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2865%2980306-7

10.1016/S0022-3476(65)80306-7

7 January 2021

Identifiers

DOI

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14 December 2019

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