(Q24621350)

2

0 references

H Goto

3

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S Sonta

4

0 references

A Matsumoto

5

0 references

C T Caskey

Journal of Clinical Investigation

6

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language of work or name

English

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publication date

September 1989

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published in

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volume

84

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issue

3

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page(s)

1024-7

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cites work

A FAMILIAL DISORDER OF URIC ACID METABOLISM AND CENTRAL NERVOUS SYSTEM FUNCTION

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Duchenne muscular dystrophy (DMD) in a female with an X/autosome translocation: further evidence that the DMD locus is at Xp21.

7 April 2017

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Isolation of a genomic clone partially encoding human hypoxanthine phosphoribosyltransferase

27 September 2017

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Cloned cDNA sequences of the hypoxanthine/guanine phosphoribosyltransferase gene from a mouse neuroblastoma cell line found to have amplified genomic sequences

27 September 2017

1 reference

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Two anonymous X-specific human sequences detecting restriction fragment length polymorphisms in region Xq26?qter

27 September 2017

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Enzyme Defect Associated with a Sex-Linked Human Neurological Disorder and Excessive Purine Synthesis

27 September 2017

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X-chromosome inactivation and developmental patterns in mammals

27 September 2017

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Fine structure of the human hypoxanthine phosphoribosyltransferase gene

27 September 2017

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Methylation of the mouse hprt gene differs on the active and inactive X chromosomes

27 September 2017

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Control of chromosome inactivation

27 September 2017

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X chromosome constitution and the human female phenotype

27 September 2017

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Hemophilia A in a Phenotypically Normal Female with XX/XO Mosaicism

30 May 2018

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Variant of factor IX deficiency in female with 45, X Turner's syndrome

30 May 2018

1 reference

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Molecular analysis of a constitutional X-autosome translocation in a female with muscular dystrophy

30 May 2018

1 reference

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The molecular basis of severe hemophilia B in a girl

30 May 2018

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Determination of clonality in acute nonlymphocytic leukemia by restriction fragment length polymorphism and methylation analysis

30 May 2018

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Human hypoxanthine-guanine phosphoribosyltransferase. Complete amino acid sequence of the erythrocyte enzyme

30 May 2018

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12 December 2020

Hypoxanthine-guanine phosphoribosyl transferase (HGPRT) deficiency in a girl

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Drug sensitivity as a genetic marker for human cell lines

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Electrophoresis of phosphoglycerate kinase

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12 December 2020

Lesch-Nyhan Syndrome: Rapid Detection of Heterozygotes by Use of Hair Follicles

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12 December 2020