(Q78985563)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13739609%20AND%20SRC:MED&resulttype=core&format=json

18 December 2019

title

Chromosomal aberrations in man (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13739609%20AND%20SRC:MED&resulttype=core&format=json

18 December 2019

author name string

S RAPPOPORT

series ordinal

1

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13739609%20AND%20SRC:MED&resulttype=core&format=json

18 December 2019

W D KAPLAN

series ordinal

2

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13739609%20AND%20SRC:MED&resulttype=core&format=json

18 December 2019

publication date

1 September 1961

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13739609%20AND%20SRC:MED&resulttype=core&format=json

The Journal of Pediatrics

18 December 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13739609%20AND%20SRC:MED&resulttype=core&format=json

18 December 2019

volume

59

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13739609%20AND%20SRC:MED&resulttype=core&format=json

18 December 2019

page(s)

415-438

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13739609%20AND%20SRC:MED&resulttype=core&format=json

A morphological distinction between neurones of the male and female, and the behaviour of the nucleolar satellite during accelerated nucleoprotein synthesis

18 December 2019

cites work

1 reference

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THE CHROMOSOME NUMBER OF MAN

7 January 2021

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Sex chromatin and phenotype in man

7 January 2021

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Chromatin test in Klinefelter's syndrome

7 January 2021

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Testicular dysgenesis affecting the seminiferous tubules principally, with chromatin-positive nuclei

7 January 2021

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Chromosomal sex in Turner's syndrome with coarctation of the aorta

7 January 2021

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Chromosomal sex in ovarian agenesis

7 January 2021

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7 January 2021

The Chromosomes of Man

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Human Somatic Chromosomes

7 January 2021

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Chromosome preparations of leukocytes cultured from human peripheral blood

7 January 2021

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Observations on the satellited human chromosomes

7 January 2021

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Heterochromatic regions and nucleolus organizers in chromosomes of the mouse, Mus musculus

7 January 2021

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The centromeric and nucleolus-associated heterochromatin of Rattus norvegicus

7 January 2021

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Formation of the sex chromatin by a single X-chromosome in liver cells of Rattus norvegicus

7 January 2021

1 reference

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On isopycnotic behavior of the XX-bivalent in oocytes of Rattus norvegicus

7 January 2021

1 reference

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On the end-to-end association of the X and Y chromosomes of Mus musculus

7 January 2021

1 reference

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Smears from the oral mucosa in the detection of chromosomal sex

7 January 2021

1 reference

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A morphological sex difference in the polymorphonuclear neutrophil leucocytes

7 January 2021

1 reference

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The basis of nuclear sex difference in somatic cells of the opossum Didelphis virginiana

7 January 2021

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On the sex chromatin of Gallus domesticus

7 January 2021

1 reference

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A single heteropycnotic chromosome in a human tumour

7 January 2021

1 reference

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The single-X nature of sex chromatin in man

7 January 2021

1 reference

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Malformation syndrome in man associated with triploidy (69 chromosomes)

7 January 2021

1 reference

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Sex in Relation to Chromosomes and Genes

7 January 2021

1 reference

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Abnormalities involving the X chromosome in women

7 January 2021

1 reference

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Human intersex with chromosome mosaicism of type XY/XO. Report of a case

7 January 2021

1 reference

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Interpretation of chromosome counts made on bone-marrow cells

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2861%2980297-7

Syndrome Characterized by Gynecomastia, Aspermatogenesis without A-Leydigism, and Increased Excretion of Follicle-Stimulating Hormone1

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2861%2980297-7

Chromation-positive Klinefelter's syndrome (primary microrchidism) in a mental-deficiency hospital.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2861%2980297-7

Psychopathology of Klinefelter's syndrome; review of thirty-one cases

7 January 2021

1 reference

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The prepubertal testicular lesion in chromatin-positive Klinefelter's syndrome (primary micro-orchidism) as seen in mentally handicapped children

7 January 2021

1 reference

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Sex reversal in newborn babies

7 January 2021

1 reference

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A case of human intersexuality having a possible XXY sex-determining mechanism

7 January 2021

1 reference

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A Presumptive Human XXY/XX Mosaic

7 January 2021

1 reference

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7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2861%2980297-7

Mongolian idiocy (mongolism) and maternal age

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2861%2980297-7

Primary amentia and micro-orchidism associated with an XXXY sex-chromosome constitution.

7 January 2021

1 reference

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THE "DOUBLE MALE": A NEW CHROMOSOME CONSTITUTION IN KLINEFELTER'S SYNDROME

7 January 2021

1 reference

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Klinefelter's syndrome: genetic studies

7 January 2021

1 reference

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Nuclear sex in familial gonadal dysgenesis

7 January 2021

1 reference

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Dystrophia myotonica, with special reference to endocrine function (Klinefelter's syndrome)

7 January 2021

1 reference

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A SYNDROME OF INFANTILISM, CONGENITAL WEBBED NECK, AND CUBITUS VALGUS1

7 January 2021

1 reference

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

7 January 2021

1 reference

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THE SOMATIC CHROMOSOMAL CONSTITUTION OF SOME HUMAN SUBJECTS WITH GENETIC DEFECTS

7 January 2021

1 reference

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Gonadal dysgenesis: the genetic significance of unusual variants

7 January 2021

1 reference

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Chromosomes in a Case of Pure Gonadal Dysgenesis

7 January 2021

1 reference

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Gonadal dysgenesis in normal-looking females; a genetic theory to explain variability of the syndrome

7 January 2021

1 reference

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Gonadal dysgenesis with androgenic manifestations in the tall eunuchoid female

7 January 2021

1 reference

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GONADAL DYSGENESIS IN THREE SISTERS

7 January 2021

1 reference

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Chromosomal sex in the syndrome of testicular feminisation

7 January 2021

1 reference

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Genetic, developmental and hormonal aspects of gonadal dysgenesis and sex inversion in man

7 January 2021

1 reference

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Evidence for the existence of the human "super female".

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2861%2980297-7

Fertility and oligophrenia in an apparent triplo-X female

7 January 2021

1 reference

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The XXX syndrome frequency among mental defectives and fertility

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2861%2980297-7

Trisomic condition of a large chromosome in a woman with mongoloid traits

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2861%2980297-7

Trisomy of a large chromosome. Association with mental retardation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2861%2980297-7

A child with 49 chromosomes

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2861%2980297-7

Chromosomes of a True Hermaphrodite

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2861%2980297-7

The chromosome complement in true hermaphroditism

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2861%2980297-7

Chromosomal constitution and nuclear sex of a true hermaphrodite

7 January 2021

1 reference

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Haemophilia A in a "girl" with male sex-chromatin pattern

7 January 2021

1 reference

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The inheritance of muscular dystrophy: further observations

7 January 2021

1 reference

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Maternal age in familial mongolism

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2861%2980297-7

A Mongol girl with 46 chromosomes

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2861%2980297-7

Chromosomal translocations in mongolism and in normal relatives

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2861%2980297-7

Chromosome translocation as a cause of familial mongolism

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2861%2980297-7

Chromosomal abnormalities in father and Mongol child

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2861%2980297-7

The chromosomes in a patient showing both mongolism and the Klinefelter syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2861%2980297-7

Klinefelter's Syndrome and Mongolism in the Same Person

7 January 2021

1 reference

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Klinefelter's syndrome in a ten-month-old mongolian idiot: report of a case with chromosome analysis

7 January 2021

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Multiple congenital anomaly caused by an extra autosome

7 January 2021

1 reference

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7 January 2021

A new trisomic syndrome

1 reference

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A new autosomal trisomy syndrome: multiple congenital anomalies caused by an extra chromosome

7 January 2021

1 reference

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Chromosomal trisomy associated with the Sturge-Weber syndrome

7 January 2021

1 reference

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A Possible Specific Chromosome Abnormality in Human Chronic Myeloid Leukæmia

7 January 2021

1 reference

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Cytogenetic studies in chronic myeloid leukaemia and acute leukaemia associated with monogolism

7 January 2021

1 reference

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THE Y-CHROMOSOME AS THE BEARER OF MALE DETERMINING FACTORS IN THE MOUSE

7 January 2021

1 reference

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Y-chromosome inheritance of hairy ears

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2861%2980297-7

Genes on the Y chromosome influencing rate of maturation in man: skeletal age studies in children with Klinefelter's (XXY) and Turner's (XO) syndromes

7 January 2021

1 reference

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Colour-blindness in ovarian agenesis (gonadal dysplasia)

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2861%2980297-7

Peculiar color blindness in peculiar people

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2861%2980297-7

10.1016/S0022-3476(61)80297-7

7 January 2021

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13739609%20AND%20SRC:MED&resulttype=core&format=json

18 December 2019

1 reference