(Q68298877)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1673960%20AND%20SRC:MED&resulttype=core&format=json

23 September 2019

title

Genetic mapping of 12 marker loci in the Xp22.3-p21.2 region (English)

1 reference

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23 September 2019

3

1 reference

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23 September 2019

Albert de la Chapelle

6

object named as

A de la Chapelle

1 reference

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23 September 2019

author name string

T Alitalo

1

1 reference

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23 September 2019

T A Kruse

2

1 reference

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23 September 2019

H M Albertsen

4

1 reference

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23 September 2019

A W Eriksson

5

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23 September 2019

publication date

1 April 1991

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23 September 2019

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23 September 2019

volume

86

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23 September 2019

page(s)

599-603

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23 September 2019

issue

6

1 reference

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https://scigraph.springernature.com/pub.10.1007/bf00201548

23 September 2019

exact match

0 references

cites work

Mapping of human X-linked hypophosphataemic rickets by multilocus linkage analysis

1 reference

12 December 2020

Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms.

1 reference

12 December 2020

Linkage relationship between retinoschisis and four marker loci

1 reference

12 December 2020

Linkage relationships between retinoschisis, Xg, and a cloned DNA sequence from the distal short arm of the X chromosome

1 reference

12 December 2020

Refined localization of the gene causing X-linked juvenile retinoschisis

1 reference

12 December 2020

DNA linkage analysis of X-linked retinoschisis

1 reference

12 December 2020

Report of the Committee on Methods of Linkage Analysis and Reporting

1 reference

12 December 2020

A genetic linkage map of the human genome.

1 reference

12 December 2020

Strategies for multilocus linkage analysis in humans

1 reference

12 December 2020

Spondyloepiphyseal dysplasia tarda: linkage with genetic markers from the distal short arm of the X chromosome

1 reference

12 December 2020

The genetic linkage map of the human X chromosome

1 reference

12 December 2020

Probable localisation of the Coffin-Lowry locus in Xp22.2-p22.1 by multipoint linkage analysis.

1 reference

12 December 2020

Bridging markers defining the map position of X linked hypophosphataemic rickets.

1 reference

12 December 2020

Chromosomal localization of ZFX--a human gene that escapes X inactivation--and its murine homologs

1 reference

12 December 2020

X-chromosome localization of the functional gene for the E1 alpha subunit of the human pyruvate dehydrogenase complex

1 reference

12 December 2020

Defective gene in lactic acidosis: abnormal pyruvate dehydrogenase E1 alpha-subunit caused by a frame shift

1 reference

12 December 2020

[The Center for the Study of Human Polymorphism]

1 reference

12 December 2020

Human and mouse amelogenin gene loci are on the sex chromosomes

1 reference

12 December 2020

Genetic mapping of four DNA markers (DXS16, DXS43, DXS85, and DXS143) from the p22 region of the human X chromosome

1 reference

12 December 2020

Agenesis of corpus callosum, ocular, and skeletal anomalies (X-linked dominant Aicardi's syndrome) in a girl with balanced X/3 translocation

1 reference

12 December 2020

Easy calculations of lod scores and genetic risks on small computers

1 reference

12 December 2020

A family with the Coffin Lowry syndrome revisited: localization of CLS to Xp21-pter.

1 reference

12 December 2020

X-linked dominant hypophosphatemia is closely linked to DNA markers DXS41 and DXS43 at Xp22

1 reference

12 December 2020

Report of the committee on the genetic constitution of the X chromosome

1 reference

12 December 2020

The human glycine receptor: a new probe that is linked to the X-linked hypophosphatemic rickets gene

1 reference

12 December 2020

Linkage relationships and gene order around the locus for X-linked retinoschisis

1 reference

12 December 2020

X-linked retinoschisis is closely linked to DXS41 and DXS16 but not DXS85

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00201548

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1673960%20AND%20SRC:MED&resulttype=core&format=json

23 September 2019

1 reference