(Q35203984)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6994494%20AND%20SRC:MED&resulttype=core&format=json

24 October 2019

title

Human neutral alpha-glucosidase C: genetic polymorphism including a "null" allele (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6994494%20AND%20SRC:MED&resulttype=core&format=json

24 October 2019

author name string

Martiniuk F

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6994494%20AND%20SRC:MED&resulttype=core&format=json

24 October 2019

Hirschhorn R

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6994494%20AND%20SRC:MED&resulttype=core&format=json

24 October 2019

language of work or name

English

0 references

publication date

1 July 1980

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6994494%20AND%20SRC:MED&resulttype=core&format=json

American Journal of Human Genetics

24 October 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6994494%20AND%20SRC:MED&resulttype=core&format=json

24 October 2019

volume

32

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6994494%20AND%20SRC:MED&resulttype=core&format=json

24 October 2019

issue

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6994494%20AND%20SRC:MED&resulttype=core&format=json

24 October 2019

page(s)

497-507

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6994494%20AND%20SRC:MED&resulttype=core&format=json

Studies on African Pygmies. 3. Peptidase C polymorphism in Babinga Pygmies: a frequent erythrocytic enzyme deficiency

24 October 2019

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1686130

Data on haptoglobin and the D group chromosomes

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1686130

The genetics of peptidase C in man.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1686130

Absence of Hexosaminidase a and B in a Normal Adult

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1686130

Characterization of unusual hexosaminidase A (HEX A) deficient human mutants

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1686130

The red-cell glutamic-pyruvate transaminase, carbonic anhydrase I and II and esterase D polymorphisms in the Ambo populations of South West Africa, with evidence for the existence of an EsD 0 allele

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1686130

Infantile and adult-onset acid maltase deficiency occurring in the same family

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1686130

Acid ?-glucosidase: A new polymorphism in man demonstrable by ?affinity? electrophoresis

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1686130

Adenosine-deaminase deficiency in a child diagnosed prenatally

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1686130

Hereditary Deficiency of Pseudocholinesterase in Eskimos

28 July 2018

1 reference

12 December 2020

[A "new" phenotype in the isoenzyme system of the human phosphoglucomutases]

1 reference

12 December 2020

Inherited quantitative variations of human phosphogluconate dehydrogenase

1 reference

12 December 2020

Alpha- and beta-thalassemia in Thailand

1 reference

12 December 2020

Hereditary deficiency of subunit H of lactate dehydrogenase

1 reference

12 December 2020

1 -Antitrypsin deficiency: a variant with no detectable 1 -antitrypsin

1 reference

12 December 2020

Inheritance of two types of deficiency of human serum cholinesterase

1 reference

12 December 2020

Silent allele as genetic basis of fucosidosis

1 reference

12 December 2020

Deficiency of adenosine deaminase not associated with severe combined immunodeficiency

1 reference

12 December 2020

Diagnosis of Homozygous α-Thalassemia in Cultured Amniotic-Fluid Fibroblasts

1 reference

12 December 2020

Genetical studies on a new variant of serum cholinesterase detected by electrophoresis

1 reference

12 December 2020

Separation of White Blood Cells

1 reference

12 December 2020

Types of Thalassaemia‐Trait Carriers as Revealed by a Study of their Incidence in Greece

1 reference

12 December 2020

Identifiers

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6994494%20AND%20SRC:MED&resulttype=core&format=json

24 October 2019

PubMed publication ID

6994494

1 reference