(Q33675587)

28 July 2017

title

Molecular genetics of human chromosome 16. (English)

1 reference

28 July 2017

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Sutherland GR

1

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28 July 2017

Reeders S

2

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28 July 2017

Hyland VJ

3

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28 July 2017

Callen DF

4

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28 July 2017

Fratini A

5

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28 July 2017

Mulley JC

6

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28 July 2017

language of work or name

English

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publication date

1 August 1987

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Journal of Medical Genetics

28 July 2017

published in

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28 July 2017

volume

24

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28 July 2017

issue

8

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28 July 2017

page(s)

451-456

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Hemoglobin H disease and multiple congenital anomalies in a child of northern European origin.

28 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050200

The rare alpha-thalassemia-1 of blacks is a zeta alpha-thalassemia-1 associated with deletion of all alpha- and zeta-globin genes.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050200

The haemoglobin H disease mental retardation syndrome: molecular studies on the South African case.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050200

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050200

Isolation and sequence of a rat chymotrypsin B gene

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050200

Human metallothionein genes are clustered on chromosome 16

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050200

Metallothionein gene cluster is split by chromosome 16 rearrangements in myelomonocytic leukaemia

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050200

Multiple, distinct forms of bovine and human protein kinase C suggest diversity in cellular signaling pathways

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050200

A mouse-human hybrid cell panel for mapping human chromosome 16.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050200

Localization of the human haptoglobin genes distal to the fragile site at 16q22 using in situ hybridization

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050200

New regional localisations for HAGH and PGP on human chromosome 16

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050200

Analysis of the human alpha-globin gene cluster reveals a highly informative genetic locus

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050200

Two genetic markers closely linked to adult polycystic kidney disease on chromosome 16.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050200

A highly polymorphic locus on chromosome 16q revealed by a probe from a chromosome-specific cosmid library

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050200

Localization of the haptoglobin alpha and beta genes (HPA and HPB) to human chromosome 16q22 by in situ hybridization

21 June 2018

1 reference

12 December 2020

Exclusion mapping illustrated by the MNSs blood group

1 reference

12 December 2020

Report of the Committee on the Genetic Constitution of Chromosomes 13, 14, 15 and 16

1 reference

12 December 2020

A highly polymorphic DNA marker linked to adult polycystic kidney disease on chromosome 16

1 reference

12 December 2020

A study of genetic linkage heterogeneity in adult polycystic kidney disease

1 reference

12 December 2020

Identifiers

0 references

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28 July 2017

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