(Q62712626)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7927339%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

title

Nondisjunction of human acrocentric chromosomes: studies of 432 trisomic fetuses and liveborns (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7927339%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7927339%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

author name string

M V Zaragoza

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7927339%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

P A Jacobs

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7927339%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

R S James

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7927339%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

S Sherman

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7927339%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

T Hassold

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7927339%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

publication date

1 October 1994

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7927339%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7927339%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

volume

94

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7927339%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

issue

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7927339%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

page(s)

411-417

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7927339%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1007/bf00201603

28 October 2019

exact match

0 references

cites work

The parental origin of the extra X chromosome in 47,XXX females.

1 reference

12 December 2020

The meiotic stage of nondisjunction in trisomy 21: determination by using DNA polymorphisms

1 reference

12 December 2020

Mitotic errors in somatic cells cause trisomy 21 in about 4.5% of cases and are not associated with advanced maternal age

1 reference

12 December 2020

Maternal uniparental disomy for human chromosome 14, due to loss of a chromosome 14 from somatic cells with t(13;14) trisomy 14.

1 reference

12 December 2020

Nondisjunction of chromosome 21.

1 reference

12 December 2020

XY chromosome nondisjunction in man is associated with diminished recombination in the pseudoautosomal region

1 reference

12 December 2020

Parental origin of the extra chromosome in trisomy 21 as indicated by analysis of DNA polymorphisms. Down Syndrome Collaborative Group

1 reference

12 December 2020

Trisomy 13 ascertained in a survey of spontaneous abortions

1 reference

12 December 2020

Parental origin of the extra chromosome in trisomy 18.

1 reference

12 December 2020

Paternal nondisjunction in trisomy 21: excess of male patients

1 reference

12 December 2020

Microsatellite polymorphism linkage map of human chromosome 13q.

1 reference

12 December 2020

Trisomy 21: association between reduced recombination and nondisjunction

1 reference

12 December 2020

Multiplex PCR of three dinucleotide repeats in the Prader-Willi/Angelman critical region (15q11-q13): molecular diagnosis and mechanism of uniparental disomy.

1 reference

12 December 2020

Genetic imprinting suggested by maternal heterodisomy in nondeletion Prader-Willi syndrome.

1 reference

12 December 2020

Molecular studies of non-disjunction in trisomy 16.

1 reference

12 December 2020

Normal phenotype with paternal uniparental isodisomy for chromosome 21.

1 reference

12 December 2020

Maternal uniparental disomy 22 has no impact on the phenotype

1 reference

12 December 2020

Nondisjunction of chromosome 15: origin and recombination

1 reference

12 December 2020

Molecular studies of trisomy 18

1 reference

12 December 2020

Alphoid DNA polymorphisms for chromosome 21 can be distinguished from those of chromosome 13 using probes homologous to both

1 reference

12 December 2020

Cytogenetic and molecular studies of trisomy 13.

1 reference

12 December 2020