(Q70566104)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5106368%20AND%20SRC:MED&resulttype=core&format=json

reason for preferred rank

12 October 2019

title

Patau's syndrome with D1 duplication-deficiency derived from a maternal D group pericentric inversion (English)

1 reference

https://api.crossref.org/works/10.1111/J.1469-1809.1956.TB01376.X

17 April 2023

Patau's syndrome with D 1 duplication-deficenncy derived from a maternal D group pericentric inversion (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5106368

17 April 2023

Patau's syndrome with D1 duplication‐deficiency derived from a maternal D group pericentric inversion (English)

1 reference

https://api.crossref.org/works/10.1111/J.1469-1809.1956.TB01376.X

17 December 2023

main subject

human chromosomes 13-15

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5106368

17 April 2023

trisomy

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5106368

17 April 2023

1 reference

https://api.crossref.org/works/10.1111/J.1469-1809.1956.TB01376.X

17 April 2023

author name string

J. M. Parrington

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5106368

17 April 2023

J. H. Edwards

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5106368

17 April 2023

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=5106368

17 April 2023

publication date

1 July 1971

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5106368%20AND%20SRC:MED&resulttype=core&format=json

full work available at URL

12 October 2019

https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1111%2Fj.1469-1809.1956.tb01376.x

1 reference

https://api.crossref.org/works/10.1111/J.1469-1809.1956.TB01376.X

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1469-1809.1956.tb01376.x/fullpdf

17 April 2023

1 reference

https://api.crossref.org/works/10.1111/J.1469-1809.1956.TB01376.X

https://onlinelibrary.wiley.com/doi/pdf/10.1111/j.1469-1809.1956.tb01376.x

17 April 2023

1 reference

https://api.crossref.org/works/10.1111/J.1469-1809.1956.TB01376.X

17 December 2023

published in

Annals of Human Genetics

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5106368%20AND%20SRC:MED&resulttype=core&format=json

12 October 2019

volume

35

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5106368%20AND%20SRC:MED&resulttype=core&format=json

12 October 2019

issue

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5106368%20AND%20SRC:MED&resulttype=core&format=json

12 October 2019

page(s)

35-45

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5106368%20AND%20SRC:MED&resulttype=core&format=json

AN ABERRANT AUTOSOME (13-15) IN A HUMAN FEMALE AND HER FATHER, BOTH APPARENTLY NORMAL

12 October 2019

cites work

3

1 reference

https://api.crossref.org/works/10.1111/J.1469-1809.1956.TB01376.X

Pericentric inversion in a group D chromosome (13?15) associated with amenorrhea and gonadal dysgenesis

17 April 2023

5

1 reference

https://api.crossref.org/works/10.1111/J.1469-1809.1956.TB01376.X

An aberrant small acrocentric chromosome

17 April 2023

8

1 reference

https://api.crossref.org/works/10.1111/J.1469-1809.1956.TB01376.X

Pericentric inversion of chromosome 21. A possible further cytogenetic mechanism in mongolism

17 April 2023

10

1 reference

https://api.crossref.org/works/10.1111/J.1469-1809.1956.TB01376.X

An apparently identical extra autosome in two severely retarded sisters with multiple malformations.

17 April 2023

13

1 reference

https://api.crossref.org/works/10.1111/J.1469-1809.1956.TB01376.X

NUCLEAR ABNORMALITIES OF THE NEUTROPHILS IN D1 (13-15)-TRISOMY SYNDROME

17 April 2023

16

1 reference

https://api.crossref.org/works/10.1111/J.1469-1809.1956.TB01376.X

Pericentric inversion of a group C autosome: a study of three families

17 April 2023

17

1 reference

https://api.crossref.org/works/10.1111/J.1469-1809.1956.TB01376.X

Familial transmission of a translocation between two non-homologous large acrocentric chromosomes. Clinical, cytogenetic and autoradiographic studies

17 April 2023

18

1 reference

https://api.crossref.org/works/10.1111/J.1469-1809.1956.TB01376.X

CHROMOSOME STUDIES IN FIVE CASES OF COLOBOMA OF THE IRIS

17 April 2023

20

1 reference

https://api.crossref.org/works/10.1111/J.1469-1809.1956.TB01376.X

Chromosome preparations of leukocytes cultured from human peripheral blood

17 April 2023

22

1 reference

https://api.crossref.org/works/10.1111/J.1469-1809.1956.TB01376.X

Multiple congenital anomaly caused by an extra autosome

17 April 2023

24

1 reference

https://api.crossref.org/works/10.1111/J.1469-1809.1956.TB01376.X

Deoxyribonucleic acid replication and mapping of the D-1 chromosome. A study of two patients with partial trisomy D-1

17 April 2023

27

1 reference

https://api.crossref.org/works/10.1111/J.1469-1809.1956.TB01376.X

Structural chromosome anomaly in a case of multiple malformation

17 April 2023

25

1 reference

https://api.crossref.org/works/10.1111/J.1469-1809.1956.TB01376.X

17 December 2023

Identifiers

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5106368%20AND%20SRC:MED&resulttype=core&format=json

12 October 2019

1 reference