(Q69902893)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2886420%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

title

Three cases of 45,X/46,XYnf mosaicism. Molecular analysis revealed heterogeneity of the nonfluorescent Y chromosome (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2886420%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

1 reference

D Gänshirt-Ahlert

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2886420%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

I H Pawlowitzki

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2886420%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

A Gal

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2886420%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

publication date

1 June 1987

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2886420%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2886420%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

volume

76

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2886420%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

issue

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2886420%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

page(s)

153-156

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2886420%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1007/bf00284913

6 October 2019

exact match

0 references

cites work

Distamycin A-DAPI banding of nonfluorescent Y(Ynf) chromosomes in 45,X/46,XYnf mosaicism

1 reference

12 December 2020

A deletion map of the human Y chromosome based on DNA hybridization

1 reference

12 December 2020

Regional assignment of a 2.1-kb repetitive sequence to the distal part of the human Y heterochromatin

1 reference

12 December 2020

X-linked dominant Charcot-Marie-Tooth disease: suggestion of linkage with a cloned DNA sequence from the proximal Xq.

1 reference

12 December 2020

Hae III restriction of DNA from three cases with nonfluorescent Y chromosomes (45XO/46XYnf)

1 reference

12 December 2020

Quantitative analysis of sex-chromosome mosaicism with X-Y DNA probes

1 reference

12 December 2020

Occurrence of tumors in dysgenetic gonads

1 reference

12 December 2020

Repeated sequence specific to human males

1 reference

12 December 2020

Human XX males with Y single-copy DNA fragments

1 reference

12 December 2020

Detection of specific sequences among DNA fragments separated by gel electrophoresis

1 reference

12 December 2020

Single-copy sequence hybridizes to polymorphic and homologous loci on human X and Y chromosomes

1 reference

12 December 2020

Small deletions of the short arm of the Y chromosome in 46,XY females

1 reference

12 December 2020

An XmnI RFLP at the subtelomeric Xp locus DXS31 [HGM7, LA, 1985]

1 reference

12 December 2020

Gonadoblastoma and Y-chromosome fluorescence

1 reference

12 December 2020

A DNA fragment from the human X chromosome short arm which detects a partially homologous sequence on the Y chromosomes long arm.

1 reference

12 December 2020

The relationship of neoplasia to disorders of abnormal sexual differentiation

1 reference

12 December 2020

A 45,X male with Y-specific DNA translocated onto chromosome 15

1 reference

12 December 2020

Atypical gonadal dysgenesis: the role of Yq in determining phenotype and malignancy risk

1 reference

12 December 2020

Nonfluorescent Y chromosomes. Cytologic evidence of origin

1 reference

12 December 2020

The identification of a repeated DNA sequence involved in the karyotype polymorphism of the human Y chromosome

1 reference

12 December 2020

Unusual scarcity of restriction site polymorphism in the human thyroglobulin gene. A linkage study suggesting autosomal dominance of a defective thyroglobulin allele

1 reference

12 December 2020