(Q39886266)

15 September 2017

Non-inactivation of an X-Chromosome Locus in Man (English)

1 reference

https://api.crossref.org/works/10.1126/SCIENCE.156396

17 December 2022

author name string

L. J. Shapiro

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A156396

17 December 2022

T. Mohandas

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A156396

17 December 2022

R. Weiss

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A156396

17 December 2022

G. Romeo

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A156396

17 December 2022

language of work or name

English

0 references

publication date

1 June 1979

1 reference

15 September 2017

15 June 1979

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=156396

full work available at URL

17 December 2022

https://syndication.highwire.org/content/doi/10.1126/science.156396

1 reference

https://api.crossref.org/works/10.1126/SCIENCE.156396

17 December 2022

1 reference

15 September 2017

204

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15 September 2017

1224-1226

1 reference

15 September 2017

4398

1 reference

Linkage relations of X-borne ichthyosis to the Xg blood groups and to other markers of the X in Israelis

15 September 2017

1

1 reference

https://api.crossref.org/works/10.1126/SCIENCE.156396

Mosaicism for sulfoiduronate sulfatase deficiency in carriers of Hunter's syndrome

17 December 2022

3

1 reference

https://api.crossref.org/works/10.1126/SCIENCE.156396

Hypohidrotic ectodermal dysplasia. A study of sweat pores in the X-linked form and in a family with probable autosomal recessive inheritance

17 December 2022

4

1 reference

https://api.crossref.org/works/10.1126/SCIENCE.156396

DEMONSTRATION OF TWO POPULATIONS OF CELLS IN THE HUMAN FEMALE HETEROZYGOUS FOR GLUCOSE-6-PHOSPHATE DEHYDROGENASE VARIANTS.

17 December 2022

5

1 reference

https://api.crossref.org/works/10.1126/SCIENCE.156396

Human phosphoglycerate kinase and inactivation of the X chromosome

17 December 2022

6

1 reference

https://api.crossref.org/works/10.1126/SCIENCE.156396

KARYOTYPE-PHENOTYPE CORRELATIONS IN GONADAL DYSGENESIS AND THEIR BEARING ON THE PATHOGENESIS OF MALFORMATIONS

17 December 2022

8

1 reference

https://api.crossref.org/works/10.1126/SCIENCE.156396

17 December 2022

9

22

460

1970

1 reference

https://api.crossref.org/works/10.1126/SCIENCE.156396

Xg Locus : Failure to detect Inactivation in Females with Chronic Myelocytic Leukaemia

17 December 2022

10

1 reference

https://api.crossref.org/works/10.1126/SCIENCE.156396

17 December 2022

11

20

564

1968

1 reference

https://api.crossref.org/works/10.1126/SCIENCE.156396

Diminished sweat pores in hypohidrotic ectodermal dysplasia: a new method for assessment.

17 December 2022

12

1 reference

https://api.crossref.org/works/10.1126/SCIENCE.156396

Advances in human genetics

17 December 2022

13

7

99

1976

1 reference

https://api.crossref.org/works/10.1126/SCIENCE.156396

Expression of two X-linked genes in human hair follicles of double heterozygotes

17 December 2022

15

1 reference

https://api.crossref.org/works/10.1126/SCIENCE.156396

Gene effect in carriers of anhidrotic ectodermal dysplasia

17 December 2022

16

1 reference

https://api.crossref.org/works/10.1126/SCIENCE.156396

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

17 December 2022

18

1 reference

https://api.crossref.org/works/10.1126/SCIENCE.156396

Locus on human X chromosome for dihydrotestosterone receptor and androgen insensitivity

17 December 2022

19

1 reference

https://api.crossref.org/works/10.1126/SCIENCE.156396

17 December 2022

20

29

448

1977

1 reference

https://api.crossref.org/works/10.1126/SCIENCE.156396

17 December 2022

21

26

360

1974

1 reference

https://api.crossref.org/works/10.1126/SCIENCE.156396

X-linked hypoxanthine-guanine phosphoribosyl transferase deficiency: heterozygote has two clonal populations.

17 December 2022

22

1 reference

https://api.crossref.org/works/10.1126/SCIENCE.156396

17 December 2022

24

43

1

1950

1 reference

https://api.crossref.org/works/10.1126/SCIENCE.156396

17 December 2022

26

28

332

1976

1 reference

https://api.crossref.org/works/10.1126/SCIENCE.156396

17 December 2022

27

28

496

1976

1 reference

https://api.crossref.org/works/10.1126/SCIENCE.156396

17 December 2022

28

28

506

1976

1 reference

https://api.crossref.org/works/10.1126/SCIENCE.156396

Genetic inactivation of the alpha-galactosidase locus in carriers of Fabry's disease

17 December 2022

29

1 reference

https://api.crossref.org/works/10.1126/SCIENCE.156396

Single-allele expression at an X-linked hyperuricemia locus in heterozygous human cells

17 December 2022

30

1 reference

https://api.crossref.org/works/10.1126/SCIENCE.156396

Steroid sulfatase deficiency

17 December 2022

33

1 reference

https://api.crossref.org/works/10.1126/SCIENCE.156396

X-linked ichthyosis: linkage relationship with the Xg blood groups and other studies in a large Dutch kindred.

17 December 2022

35

1 reference

https://api.crossref.org/works/10.1126/SCIENCE.156396

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

17 December 2022

36

1 reference

https://api.crossref.org/works/10.1126/SCIENCE.156396

17 December 2022

Identifiers

1 reference

15 September 2017

1 reference