(Q74451712)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13414769%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

title

[Mutation and phenocopy in mammals and man; their theoretical and practical importance for genetics and eugenics] (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13414769%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

author name string

H NACHTSHEIM

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13414769%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

publication date

1 February 1957

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13414769%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13414769%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

volume

13

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13414769%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

issue

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13414769%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

page(s)

57-68

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13414769%20AND%20SRC:MED&resulttype=core&format=json

[Genetics and mutation rate of retinoblastoma (glioma retinae), with general remarks on methods of determining mutation rate in humans]

10 November 2019

cites work

1 reference

12 December 2020

[Brief introduction to teratology.]

1 reference

12 December 2020

HEREDITARY BRACHYDACTYLIA AND ALLIED ABNORMALITIES IN THE RABBIT

1 reference

12 December 2020

[The causes of malformations and deformity diseases]

1 reference

12 December 2020

[Phenocopy of the blood picture of homozygotic Pelger's anomaly caused by reactive deviation to the left in a heterozygotic Pelger's anomaly]

1 reference

12 December 2020

1 reference

12 December 2020

[An unusual form of the hemorrhagic diathesis.]

1 reference

12 December 2020

[Etiological role of the genes and phenocopies in human abnormalities]

1 reference

12 December 2020

The effects of a lethal mutation responsible for duplications and twinning in mouse embryos

1 reference

12 December 2020

Homozygous form of Pelger-Huët's nuclear anomaly in man

1 reference

12 December 2020

Two different mutations of the X-chromosome causing diabetes insipidus

1 reference

12 December 2020

Familial osseous atrophy

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF02160092

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13414769%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

1 reference