Molecular detection of a translocation (Y;11) (q11.2;q24) in a 45,X male with signs of Jacobsen syndrome (Q35933988)

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English	Molecular detection of a translocation (Y;11) (q11.2;q24) in a 45,X male with signs of Jacobsen syndrome	scientific article

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scholarly article

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Europe PubMed Central

PubMed publication ID

1551671

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11 August 2017

review article

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Europe PubMed Central

title

Molecular detection of a translocation (Y;11) (q11.2;q24) in a 45,X male with signs of Jacobsen syndrome (English)

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PubMed publication ID

1551671

retrieved

11 August 2017

author name string

J O Van Hemel

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1

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Europe PubMed Central

PubMed publication ID

1551671

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11 August 2017

B Eussen

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2

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Europe PubMed Central

PubMed publication ID

1551671

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11 August 2017

E Wesby-van Swaay

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3

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Europe PubMed Central

PubMed publication ID

1551671

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11 August 2017

B A Oostra

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4

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Europe PubMed Central

PubMed publication ID

1551671

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11 August 2017

publication date

1 March 1992

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Europe PubMed Central

PubMed publication ID

1551671

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11 August 2017

published in

Human Genetics

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Europe PubMed Central

PubMed publication ID

1551671

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11 August 2017

volume

88

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Europe PubMed Central

PubMed publication ID

1551671

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11 August 2017

issue

6

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Europe PubMed Central

PubMed publication ID

1551671

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11 August 2017

page(s)

661-667

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Europe PubMed Central

PubMed publication ID

1551671

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11 August 2017

cites work

Seven polymorphic loci mapping to human chromosomal region 11q22-qter

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/1551671

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12 December 2020

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Distal 11q monosomy. The typical 11q monosomy syndrome is due to deletion of subband 11q24.1

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https://pubmed.ncbi.nlm.nih.gov/1551671

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A Y/5 translocation in a 45,X male with cri du chat syndrome

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/1551671

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12 December 2020

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A 45,X male with molecular evidence of a translocation of Y euchromatin onto chromosome 1.

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https://pubmed.ncbi.nlm.nih.gov/1551671

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12 December 2020

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Review and hypotheses: somatic mosaicism: observations related to clinical genetics

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https://pubmed.ncbi.nlm.nih.gov/1551671

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12 December 2020

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Distal 11q deletion: a specific clinical entity

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/1551671

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12 December 2020

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Exclusion of chromosomal mosaicism: tables of 90%, 95% and 99% confidence limits and comments on use

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https://pubmed.ncbi.nlm.nih.gov/1551671

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The origin and phenotype of XO males

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https://pubmed.ncbi.nlm.nih.gov/1551671

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12 December 2020

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Partial deletion of long arm of chromosome 11[del(11)(q23)]: Jacobsen syndrome. Two new cases and review of the clinical findings

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https://pubmed.ncbi.nlm.nih.gov/1551671

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12 December 2020

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A sterile male with 45,X0 and a Y;22 translocation

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https://pubmed.ncbi.nlm.nih.gov/1551671

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12 December 2020

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XO and male phenotype

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https://pubmed.ncbi.nlm.nih.gov/1551671

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The 11q -- syndrome

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https://pubmed.ncbi.nlm.nih.gov/1551671

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An XX male: Cytogenetic and endocrine studies

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https://pubmed.ncbi.nlm.nih.gov/1551671

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12 December 2020

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Y;autosome translocations and mosaicism in the aetiology of 45,X maleness: assignment of fertility factor to distal Yq11

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https://pubmed.ncbi.nlm.nih.gov/1551671

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12 December 2020

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

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/1551671

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12 December 2020

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A fertile man with tdic(Y;22): how a stable neo-X1X2Y sex-determining mechanism could evolve in man

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https://pubmed.ncbi.nlm.nih.gov/1551671

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12 December 2020

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Rapid subchromosomal localization of cosmids by nonradioactive in situ hybridization

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https://pubmed.ncbi.nlm.nih.gov/1551671

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12 December 2020

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Genetic evidence that ZFY is not the testis-determining factor

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https://pubmed.ncbi.nlm.nih.gov/1551671

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12 December 2020

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A simple salting out procedure for extracting DNA from human nucleated cells

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https://pubmed.ncbi.nlm.nih.gov/1551671

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12 December 2020

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A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity

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https://pubmed.ncbi.nlm.nih.gov/1551671

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12 December 2020

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Detection of novel centromeric polymorphisms associated with alpha satellite DNA from human chromosome 11

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https://pubmed.ncbi.nlm.nih.gov/1551671

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12 December 2020

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Molecular detection of a translocation (Y;15) in a 45,X male

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https://pubmed.ncbi.nlm.nih.gov/1551671

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12 December 2020

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The telomeric region of the human X chromosome long arm: presence of a highly polymorphic DNA marker and analysis of recombination frequency

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https://pubmed.ncbi.nlm.nih.gov/1551671

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12 December 2020

based on heuristic

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Tandem Y/6 translocation with partial deletion 6 (p23----pter)

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https://pubmed.ncbi.nlm.nih.gov/1551671

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12 December 2020

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A gene from the human sex-determining region encodes a protein with homology to a conserved DNA-binding motif

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/1551671

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12 December 2020

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Cytogenetical and clinical investigations in four subjects with anomalies of sexual development

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/1551671

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12 December 2020

based on heuristic

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Translocation Y/5 resulting in Cri du Chat syndrome

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https://pubmed.ncbi.nlm.nih.gov/1551671

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12 December 2020

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In situ fluorescence hybridization of Y translocations: cytogenetic analysis using probes Y190 and Y431.

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/1551671

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12 December 2020

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

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/1551671

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12 December 2020

based on heuristic

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Deleted Yq in the sterile son of a man with a satellited Y chromosome (Yqs).

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/1551671

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12 December 2020

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BSu restriction of DNA from cases exhibiting sex-chromosome abnormalities

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/1551671

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12 December 2020

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A detailed genetic map of the long arm of chromosome 11

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/1551671

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular detection of a Yp/18 translocation in a 45,X holoprosencephalic male

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/1551671

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12 December 2020

based on heuristic

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An (11;21) translocation in four generations with chromosome 11 abnormalities in the offspring. A clinical, cytogenetical, and gene marker study

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/1551671

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/1551671

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12 December 2020

based on heuristic

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Male infant with cat cry syndrome and apparent absence of the Y chromosome

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/1551671

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The sex-determining region of the human Y chromosome encodes a finger protein.

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/1551671

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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

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/1551671

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A DNA probe detecting multiple haplotypes of the human Y chromosome

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1551671

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A 45,X male with a Yp/18 translocation

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1551671

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Y chromosome specific probes identify breakpoint in a 45,X/46,X,del(Y)(pter----q11.1:) karyotype of an infertile male.

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1551671

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12 December 2020

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Male development of chromosomally female mice transgenic for Sry.

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https://pubmed.ncbi.nlm.nih.gov/1551671

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12 December 2020

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Identifiers

DOI

10.1007/BF02265294

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1551671

retrieved

11 August 2017

PubMed publication ID

1551671

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1551671

retrieved

11 August 2017

 

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