Genetic heterogeneity in X-linked amelogenesis imperfecta (Q67522990)

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14 September 2019

title

Genetic heterogeneity in X-linked amelogenesis imperfecta (English)

1 reference

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14 September 2019

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amelogenesis imperfecta

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M J Aldred

1

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14 September 2019

P J Crawford

2

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14 September 2019

E Roberts

3

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14 September 2019

C M Gillespie

4

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14 September 2019

N S Thomas

5

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14 September 2019

I Fenton

6

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14 September 2019

L A Sandkuijl

7

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14 September 2019

P S Harper

8

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14 September 2019

publication date

1 November 1992

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14 September 2019

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14 September 2019

volume

14

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14 September 2019

issue

3

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14 September 2019

page(s)

567-573

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An anonymous X-chromosomal clone identifying a frequent RFLP at Xp21-22 (HGM8 provisional no. DXS207).

14 September 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2805%2980153-3

7 January 2021

Identification of a nonsense mutation in the amelogenin gene (AMELX) in a family with X-linked amelogenesis imperfecta (AIH1)

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2805%2980153-3

7 January 2021

X-linked amelogenesis imperfecta. Presentation of two kindreds and a review of the literature

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2805%2980153-3

7 January 2021

A polymorphic locus at Xq27-28 detected by the probe U6.2 [DXS304]

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2805%2980153-3

7 January 2021

An anonymous single copy X-chromosome clone DXS92, from Xq26-27, identifies two frequent RFLPs

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2805%2980153-3

7 January 2021

BclI RFLP at the DXS16 locus

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2805%2980153-3

7 January 2021

Multi-allelic RFLP for M27 beta, an anonymous single copy genomic clone at Xp11.3-Xcen [HGM9 provisional no. DXS255].

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2805%2980153-3

7 January 2021

Genetic mapping and diagnosis of haemophilia A achieved through a BclI polymorphism in the factor VIII gene

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2805%2980153-3

7 January 2021

Isolation of probes detecting restriction fragment length polymorphisms from X chromosome-specific libraries: potential use for diagnosis of Duchenne muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2805%2980153-3

7 January 2021

A deletion in the amelogenin gene (AMG) causes X-linked amelogenesis imperfecta (AIH1)

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2805%2980153-3

7 January 2021

Human and mouse amelogenin gene loci are on the sex chromosomes

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2805%2980153-3

7 January 2021

Gene action in the X-chromosome of the mouse (Mus musculus L.)

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2805%2980153-3

7 January 2021

An RFLP detecting single copy X-chromosome fragment, dic56, from Xp22-Xpter [HGM8 assignment no. DXS 143].

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2805%2980153-3

7 January 2021

A human X-Y homologous region encodes "amelogenin"

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2805%2980153-3

7 January 2021

Detection of specific sequences among DNA fragments separated by gel electrophoresis

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2805%2980153-3

7 January 2021

Partial expression of sex-linked recessive amelogenesis imperfecta in females compatible with the Lyon hypothesis

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2805%2980153-3

7 January 2021

10.1016/S0888-7543(05)80153-3

Identifiers

DOI

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14 September 2019

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