(Q72253491)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8112730%20AND%20SRC:MED&resulttype=core&format=json

25 October 2019

title

Linkage analysis of autosomal dominant atrioventricular canal defects: exclusion of chromosome 21 (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8112730%20AND%20SRC:MED&resulttype=core&format=json

25 October 2019

author name string

A J Cousineau

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8112730%20AND%20SRC:MED&resulttype=core&format=json

25 October 2019

R M Lauer

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8112730%20AND%20SRC:MED&resulttype=core&format=json

25 October 2019

M E Pierpont

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8112730%20AND%20SRC:MED&resulttype=core&format=json

25 October 2019

T L Burns

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8112730%20AND%20SRC:MED&resulttype=core&format=json

25 October 2019

R H Ardinger

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8112730%20AND%20SRC:MED&resulttype=core&format=json

25 October 2019

S R Patil

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8112730%20AND%20SRC:MED&resulttype=core&format=json

25 October 2019

V C Sheffield

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8112730%20AND%20SRC:MED&resulttype=core&format=json

25 October 2019

publication date

1 February 1994

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8112730%20AND%20SRC:MED&resulttype=core&format=json

25 October 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8112730%20AND%20SRC:MED&resulttype=core&format=json

25 October 2019

volume

93

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8112730%20AND%20SRC:MED&resulttype=core&format=json

25 October 2019

issue

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8112730%20AND%20SRC:MED&resulttype=core&format=json

25 October 2019

page(s)

103-108

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8112730%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1007/bf00210591

25 October 2019

exact match

0 references

cites work

Down syndrome: molecular mapping of the congenital heart disease and duodenal stenosis

1 reference

12 December 2020

Multifactorial inheritance hypothesis for the etiology of congenital heart diseases. The genetic-environmental interaction

1 reference

12 December 2020

Molecular genetic approach to the characterization of the "Down syndrome region" of chromosome 21.

1 reference

12 December 2020

Trisomy 16 in the mouse fetus associated with generalized edema and cardiovascular and urinary tract anomalies.

1 reference

12 December 2020

Down syndrome critical region around D21S55 on proximal 21q22.3

1 reference

12 December 2020

Familial atrial septal defect of the primum type: a report of four cases in one sibship

1 reference

12 December 2020

Third International Workshop on Human Chromosome 21.

1 reference

12 December 2020

Molecular definition of a region of chromosome 21 that causes features of the Down syndrome phenotype

1 reference

12 December 2020

Autosomal dominant inheritance of endocardial cushion defect

1 reference

12 December 2020

A simple and efficient non-organic procedure for the isolation of genomic DNA from blood

1 reference

12 December 2020

Two-dimensional echocardiography in detection of endocardial cushion defect in families

1 reference

12 December 2020

Fine structure physical mapping of the region of mouse Chromosome 10 homologous to human Chromosome 21

1 reference

12 December 2020

Abundant class of human DNA polymorphisms which can be typed using the polymerase chain reaction

1 reference

12 December 2020

Cardiac and noncardiac malformations: observations in a population-based study

1 reference

12 December 2020

Microdeletions within 22q11 associated with sporadic and familial DiGeorge syndrome.

1 reference

12 December 2020

Easy calculations of lod scores and genetic risks on small computers

1 reference

12 December 2020

Mouse trisomy 16 as an animal model of human trisomy 21 (Down syndrome): Production of viable trisomy 16 ↔ diploid mouse chimeras

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00210591

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8112730%20AND%20SRC:MED&resulttype=core&format=json

25 October 2019

1 reference