A mosaic 45,X/46,X,r(?) karyotype investigated with X and Y centromere-specific probes using a non-autoradiographic in situ hybridization technique (Q67980080)

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scientific article published on 01 December 1988

Language	Label	Description	Also known as
English	A mosaic 45,X/46,X,r(?) karyotype investigated with X and Y centromere-specific probes using a non-autoradiographic in situ hybridization technique	scientific article published on 01 December 1988

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scholarly article

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3198130%20AND%20SRC:MED&resulttype=core&format=json

20 September 2019

A mosaic 45,X/46,X,r(?) karyotype investigated with X and Y centromere-specific probes using a non-autoradiographic in situ hybridization technique (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3198130%20AND%20SRC:MED&resulttype=core&format=json

20 September 2019

author name string

J A Crolla

1

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3198130%20AND%20SRC:MED&resulttype=core&format=json

20 September 2019

J C Llerena

2

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Europe PubMed Central

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20 September 2019

publication date

1 December 1988

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20 September 2019

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3198130%20AND%20SRC:MED&resulttype=core&format=json

20 September 2019

81

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20 September 2019

1

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Europe PubMed Central

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20 September 2019

81-84

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PubMed publication ID

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20 September 2019

Combined cytogenetic techniques and non-fluorescent Y. Cytologic evidences of dic(Yp)(q11) in a previously interpreted 46,X,Yq-

1 reference

https://pubmed.ncbi.nlm.nih.gov/3198130

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mechanisms of giemsa banding of chromosomes. I. Giemsa-11 banding with azure and eosin

1 reference

https://pubmed.ncbi.nlm.nih.gov/3198130

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Organization and evolution of alpha satellite DNA from human chromosome 11.

1 reference

https://pubmed.ncbi.nlm.nih.gov/3198130

12 December 2020

based on heuristic

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Y ring chromosome associated with gonadoblastoma in situ

1 reference

https://pubmed.ncbi.nlm.nih.gov/3198130

12 December 2020

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Cytogenetic findings in 89 cases of Turner's syndrome with abnormal karyotypes

1 reference

https://pubmed.ncbi.nlm.nih.gov/3198130

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cytogenetic findings in 125 patients with Turner's syndrome and abnormal karyotypes

1 reference

https://pubmed.ncbi.nlm.nih.gov/3198130

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Characterization of human centromeric regions of specific chromosomes by means of alphoid DNA sequences

1 reference

https://pubmed.ncbi.nlm.nih.gov/3198130

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

G-11 staining in Turner's syndrome with mos 45,X/46,X,r(?)

1 reference

https://pubmed.ncbi.nlm.nih.gov/3198130

12 December 2020

based on heuristic

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The age of occurrence of gonadal tumors in intersex patients with a Y chromosome

1 reference

https://pubmed.ncbi.nlm.nih.gov/3198130

12 December 2020

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Incontinentia pigmenti and X-autosome translocations. Non-isotopic in situ hybridization with an X-centromere-specific probe (pSV2X5) reveals a possible X-centromeric breakpoint in one of five published cases

1 reference

https://pubmed.ncbi.nlm.nih.gov/3198130

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Further cytologic evidence for Xp-Yp translocation in XX males using in situ hybridization with Y-derived probe

1 reference

https://pubmed.ncbi.nlm.nih.gov/3198130

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Staining of some specific regions of human chromosomes, particularly the secondary constriction of No. 9.

1 reference

https://pubmed.ncbi.nlm.nih.gov/3198130

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Structural aberrations of the Y chromosome and the corresponding phenotype. Report of a case with the karotype 45,X-46,X,i(Yp)

1 reference

https://pubmed.ncbi.nlm.nih.gov/3198130

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Isolation and characterization of a major tandem repeat family from the human X chromosome

1 reference

https://pubmed.ncbi.nlm.nih.gov/3198130

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosomal and clinical findings in 110 females with Turner syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/3198130

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evolution of karyotypic abnormalities and C-MYC oncogene amplification in human colonic carcinoma cell lines

1 reference

https://pubmed.ncbi.nlm.nih.gov/3198130

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Isolation and characterization of an alphoid centromeric repeat family from the human Y chromosome

1 reference

https://pubmed.ncbi.nlm.nih.gov/3198130

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Nonfluorescent Y chromosomes. Cytologic evidence of origin

1 reference

https://pubmed.ncbi.nlm.nih.gov/3198130

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Detection of species specific chromosomes in somatic cell hybrids

1 reference

https://pubmed.ncbi.nlm.nih.gov/3198130

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Three cases of sex chromosome mosaicism with a nonfluorescent Y

1 reference

https://pubmed.ncbi.nlm.nih.gov/3198130

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Localisation of male determining factors in man: a thorough review of structural anomalies of the Y chromosome

1 reference

https://pubmed.ncbi.nlm.nih.gov/3198130

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Novel non-isotopic in situ hybridization technique detects small (1 Kb) unique sequences in routinely G-banded human chromosomes: fine mapping of N-myc and beta-NGF genes

1 reference

https://pubmed.ncbi.nlm.nih.gov/3198130

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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