(Q39884291)

15 September 2017

title

Double Trisomy as a Mosaic. Case History (48,XYY,+21/47,XY,+21) and Survey of the Literature of Mixed Autosomal-Gonosomal Trisomies (English)

1 reference

https://api.crossref.org/works/10.1017/S0001566000009521

14 May 2022

Double trisomy as a mosaic. Case history (48, XYY, + 21/47,XY, +21) and survey of the literature of mixed autosomal-gonosomal trisomies (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A155969

14 May 2022

author name string

G. Schwanitz

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A155969

14 May 2022

M. Hagner

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A155969

14 May 2022

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=155969

14 May 2022

publication date

1 January 1978

1 reference

full work available at URL

15 September 2017

https://www.cambridge.org/core/services/aop-cambridge-core/content/view/S0001566000009521

1 reference

https://api.crossref.org/works/10.1017/S0001566000009521

Acta geneticae medicae et gemellologiae

14 May 2022

published in

1 reference

15 September 2017

volume

27

1 reference

15 September 2017

page(s)

67-74

1 reference

Further observations of cell selection in vivo in normal-G trisomic mosaics

15 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1017%2FS0001566000009521

Trisomy G/normal mosaics in non-mongoloid mentally deficient children

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0001566000009521

7 January 2021

Klinefelter's and Down's syndrome in an adolescent with abnormal EEG.

1 reference

https://api.crossref.org/works/10.1017%2FS0001566000009521

7 January 2021

New human double trisomy or tetrasomy

1 reference

https://api.crossref.org/works/10.1017%2FS0001566000009521

7 January 2021

21 trisomy with an XYY sex chromosome complement

1 reference

https://api.crossref.org/works/10.1017%2FS0001566000009521

7 January 2021

A survey of sex-chromosome abnormalities among 4514 mental defectives.

1 reference

https://api.crossref.org/works/10.1017%2FS0001566000009521

7 January 2021

CYTOGENETICS OF DOWN'S SYNDROME (MONGOLISM). I. DATA ON A CONSECUTIVE SERIES OF PATIENTS REFERRED FOR GENETIC COUNSELLING AND DIAGNOSIS.

1 reference

https://api.crossref.org/works/10.1017%2FS0001566000009521

7 January 2021

XYY chromosomal complement, proven by fluorescence, in a child with trisomy 21:48,XYY,21+

1 reference

https://api.crossref.org/works/10.1017%2FS0001566000009521

7 January 2021

Double trisomy: trisomy 17-18 with triple X in a female infant

1 reference

https://api.crossref.org/works/10.1017%2FS0001566000009521

7 January 2021

Post-mortem diagnosis of a new double-trisomy associated with cardiovascular and other anomalies

1 reference

https://api.crossref.org/works/10.1017%2FS0001566000009521

7 January 2021

A sex chromatin survey of newborn children in two London hospitals

1 reference

https://api.crossref.org/works/10.1017%2FS0001566000009521

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1017%2FS0001566000009521

7 January 2021

A case of double trisomy: trisomy No. 18 and triplo- X

1 reference

https://api.crossref.org/works/10.1017%2FS0001566000009521

7 January 2021

Klinefelter's Syndrome and Mongolism in the Same Person

1 reference

https://api.crossref.org/works/10.1017%2FS0001566000009521

7 January 2021

Twins, probably monozygotic: one mongoloid with 48 chromosomes, the other normal.

1 reference

https://api.crossref.org/works/10.1017%2FS0001566000009521

7 January 2021

Mosaicism of X and G chromosomes.

1 reference

https://api.crossref.org/works/10.1017%2FS0001566000009521

7 January 2021

Double aneuploidy: trisomy-18 and Klinefelter's syndrome

1 reference

https://api.crossref.org/works/10.1017%2FS0001566000009521

7 January 2021

Klinefelter's syndrome and G trisomy

1 reference

https://api.crossref.org/works/10.1017%2FS0001566000009521

7 January 2021

Klinefelter‘ syndrome and trisomy 18 in a newborn boy

1 reference

https://api.crossref.org/works/10.1017%2FS0001566000009521

7 January 2021

The Klinefelter‐mongolism type of double aneuploidy

1 reference

https://api.crossref.org/works/10.1017%2FS0001566000009521

7 January 2021

DOUBLE ANEUPLOIDY: TRISOMY 21 AND XO--XX SEX CHROMOSOME MOSAICISM

1 reference

https://api.crossref.org/works/10.1017%2FS0001566000009521

7 January 2021

Down's syndrome with additional XYY aneuploidy

1 reference

https://api.crossref.org/works/10.1017%2FS0001566000009521

7 January 2021

Down's syndrome with XYY additional aneuploidy

1 reference

https://api.crossref.org/works/10.1017%2FS0001566000009521

7 January 2021

A case of 48,XXY,21+ in an infant with Down's syndrome

1 reference

https://api.crossref.org/works/10.1017%2FS0001566000009521

7 January 2021

Sex-chromosome abnormalities in a population of mentally defective children

1 reference

https://api.crossref.org/works/10.1017%2FS0001566000009521

7 January 2021

https://api.crossref.org/works/10.1017%2FS0001566000009521

1 reference

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1017%2FS0001566000009521

7 January 2021

XXX 21-trisomy and retinoblastoma

1 reference

https://api.crossref.org/works/10.1017%2FS0001566000009521

7 January 2021

Mongoloid twins with 48 chromosomes (AA + A21XXY)

1 reference

https://api.crossref.org/works/10.1017%2FS0001566000009521

7 January 2021

FAMILIAL MOSAICISM ATTRIBUTABLE TO A NEW GENE

1 reference

https://api.crossref.org/works/10.1017%2FS0001566000009521

7 January 2021

Three unusual trisomic patterns in children. Triple X plus triple E-triple X mosaic: normal XY-D trisomy mosaic; partial trisomy with E translocation

1 reference

https://api.crossref.org/works/10.1017%2FS0001566000009521

7 January 2021

Double trisomy and double trisomic mosaicism

5

1 reference

https://api.crossref.org/works/10.1017/S0001566000009521

A case of double trisomy in a liveborn infant: 48, XXY, "13

17 December 2022

15

1 reference

https://api.crossref.org/works/10.1017/S0001566000009521

Prenatal Diagnosis of Double Trisomy

17 December 2022

33

1 reference

https://api.crossref.org/works/10.1017/S0001566000009521

Turner Phenotype: Mosaic 45,X/47,XY,+18

17 December 2022

42

1 reference

https://api.crossref.org/works/10.1017/S0001566000009521

Double aneuploidy: the frequency of XXY in males with Down's syndrome

17 December 2022

48

1 reference

https://api.crossref.org/works/10.1017/S0001566000009521

The incidence of Klinefelter's syndrome in a mental deficiency hospital

17 December 2022

54

1 reference

https://api.crossref.org/works/10.1017/S0001566000009521

17 December 2022

Identifiers

1 reference

15 September 2017

1 reference