(Q70795660)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7239510%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

title

Incomplete trisomy 22. III. Mosaic-trisomy 22 and the problem of full trisomy 22 (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7239510%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

author name string

A Schinzel

series ordinal

1

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7239510%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

publication date

1 January 1981

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7239510%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7239510%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

volume

56

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7239510%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

issue

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7239510%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

page(s)

269-273

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7239510%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1007/bf00274677

13 October 2019

exact match

0 references

cites work

The "cat eye syndrome": dicentric small marker chromosome probably derived from a no.22 (tetrasomy 22pter to q11) associated with a characteristic phenotype. Report of 11 patients and delineation of the clinical picture

1 reference

12 December 2020

Precise identification of various chromosomal abnormalities.

1 reference

12 December 2020

A new contribution to the study of 22 trisomy

1 reference

12 December 2020

A familial X-22 translocation with an extra X chromosome

1 reference

12 December 2020

Familial translocation with partial trisomy of 13 and 22: evidence that specific regions of chromosomes 13 and 22 are responsible for the phenotype of each trisomy

1 reference

12 December 2020

Balanced homologous translocation t(22q22q) in a phenotypically normal woman with repeated spontaneous abortions

1 reference

12 December 2020

Trisomy 22 with 'cat eye' anomaly

1 reference

12 December 2020

A 22/22 translocation carrier with recurrent abortions demonstrated by a Giemsa banding technique

1 reference

12 December 2020

Incomplete trisomy 22. II. Familial trisomy of the distal segment of chromosome 22q in two brothers from a mother with a translocation, t(6;22)(q27;q13)

1 reference

12 December 2020

Identification by Q and G bands of chromosome anomalies in spontaneous abortion

1 reference

12 December 2020

A technique for in situ Karyotyping of primary amniotic fluid cell cultures

1 reference

12 December 2020

Recurrent abortion associated with a balanced 22;22 translocation, or isochromosome 22q in a monozygous twin

1 reference

12 December 2020

Segregation of a t(14q22q) chromosome in a large kindred

1 reference

12 December 2020

Abnormal skin fibroblast cytogenetics in four dysmorphic patients with normal lymphocyte chromosomes

1 reference

12 December 2020

Partial trisomies 13 and 22 due to nondisjunction of a maternal reciprocal translocation, t(13;22)(q22;q11)

1 reference

12 December 2020

Trisomy 22 in a newborn girl with multiple malformations

1 reference

12 December 2020

1 reference

12 December 2020

[Trisomy 22. A new case]

1 reference

12 December 2020

A case of 22-trisomy mosaic

1 reference

12 December 2020

A case of trisomy 22 with a probable Robertsonian translocation 21/22

1 reference

12 December 2020

Partial trisomy 22q with elevated arylsulfatase-A activity

1 reference

12 December 2020

Familial translocation 15-22. A possible cause for abortions in female carriers

1 reference

12 December 2020

Systematic analysis of 95 reciprocal translocations of autosomes

1 reference

12 December 2020

Incomplete trisomy 22. I. Familial 11/22 translocation with 3:1 meiotic disjunction. Delineation of a common clinical picture and report of nine new cases from six families

1 reference

12 December 2020

Cytogenetic and clinical investigations in trisomia 22 (author's transl)

1 reference

12 December 2020

Letter: Translocation 22-22?

1 reference

12 December 2020

A cytogenetic study of human spontaneous abortions using banding techniques

1 reference

12 December 2020

Trisomy 22 in a 20-year-old female.

1 reference

12 December 2020

A further case of a 22;22 Robertsonian translocation associated with recurrent abortions

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00274677

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7239510%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

1 reference