(Q39721677)

14 September 2017

title

Classification of Hereditary Cataracts in Children by Linkage Analysis (English)

1 reference

https://api.crossref.org/works/10.1016/S0161-6420(79)35365-9

sex chromosome aberration

1 May 2022

main subject

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A121767

1 May 2022

1 reference

https://api.crossref.org/works/10.1016/S0161-6420(79)35365-9

1 May 2022

author name string

I. H. Maumenee

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A121767

1 May 2022

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=121767

1 May 2022

publication date

1 September 1979

1 reference

full work available at URL

14 September 2017

https://api.elsevier.com/content/article/PII:S0161642079353659?httpAccept=text/xml

1 reference

https://api.crossref.org/works/10.1016/S0161-6420(79)35365-9

https://api.elsevier.com/content/article/PII:S0161642079353659?httpAccept=text/plain

1 May 2022

1 reference

https://api.crossref.org/works/10.1016/S0161-6420(79)35365-9

1 May 2022

1 reference

14 September 2017

volume

86

1 reference

14 September 2017

issue

9

1 reference

14 September 2017

page(s)

1554-1558

1 reference

The Linkage between the Genes for Colour-Blindness and Haemophilia in Man

14 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2879%2935365-9

7 January 2021

PROBABLE LINKAGE BETWEEN A CONGENITAL CATARACT LOCUS AND THE DUFFY BLOOD GROUP LOCUS

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2879%2935365-9

7 January 2021

CHROMOSOME DELETION IN A CASE OF RETINOBLASTOMA.

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2879%2935365-9

7 January 2021

Confirmation of the assignment of the gene for galactose-1-phosphate uridylyltransferase (E.C. 2.7.7.12) to human chromosome 9

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2879%2935365-9

7 January 2021

Assignment of the gene for galactokinase to human chromosome 17 and its regional localisation to band q21-22.

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2879%2935365-9

7 January 2021

Assignment of the human gene for galactokinase to chromosome 17.

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2879%2935365-9

7 January 2021

Galactokinase Deficiency and Cataracts

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2879%2935365-9

7 January 2021

Mannosidosis: assignment of the lysosomal alpha-mannosidase B gene to chromosome 19 in man

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2879%2935365-9

7 January 2021

Identifiers

1 reference

14 September 2017

1 reference