(Q67355184)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:669700%20AND%20SRC:MED&resulttype=core&format=json

12 September 2019

title

Cytologic observations in 35 individuals with a 5p- karyotype (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:669700%20AND%20SRC:MED&resulttype=core&format=json

12 September 2019

main subject

human chromosomes 4-5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A669700

19 July 2022

chromosome abnormality

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A669700

19 July 2022

author name string

E. Niebuhr

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A669700

19 July 2022

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=669700

19 July 2022

publication date

1 June 1978

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:669700%20AND%20SRC:MED&resulttype=core&format=json

12 September 2019

9 June 1978

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=669700

19 July 2022

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:669700%20AND%20SRC:MED&resulttype=core&format=json

12 September 2019

volume

42

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:669700%20AND%20SRC:MED&resulttype=core&format=json

12 September 2019

issue

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:669700%20AND%20SRC:MED&resulttype=core&format=json

12 September 2019

page(s)

143-156

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:669700%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1007/bf00283634

12 September 2019

exact match

0 references

cites work

[New system of chromosome banding: the T bands (author's transl)]

1 reference

12 December 2020

Exclusion of chromosomal mosaicism: tables of 90%, 95% and 99% confidence limits and comments on use

1 reference

12 December 2020

A deleted B chromosome in a mosaic mother and her cri du chat progeny

1 reference

12 December 2020

LONGITUDINAL DIFFERENTIATION OF CHROMOSOMES AND THE POSSIBILITY OF INTERSTITIAL TELOMERES

1 reference

12 December 2020

An improved technique for selective silver staining of nucleolar organizer regions in human chromosomes

1 reference

12 December 2020

Cri-du-chat and trisomy 13 syndromes in an infant with an unbalanced chromosomal translocation

1 reference

12 December 2020

Variation in the centromeric banding of chromosome 19*

1 reference

12 December 2020

CHROMOSOMAL AUTORADIOGRAPHY IN THE CRI DU CHAT SYNDROME

1 reference

12 December 2020

Clustering in deleted short-arm length among 25 cases with a Bp– chromosome

1 reference

12 December 2020

Translocation heterozygosis: a cause of five cases of the cri du chat syndrome and two cases with a duplication of chromosome number five in three families

1 reference

12 December 2020

Chromosome delection point in "cri du chat" syndrome (author's transl)

1 reference

12 December 2020

A new technic of analysis of the human karyotype

1 reference

12 December 2020

Quinacrine mustard fluorescence of human chromosomes: characterization of unusual translocations

1 reference

12 December 2020

Localization of the deleted segment in the Cri-du-Chat syndrome

1 reference

12 December 2020

Visualization of nucleolar organizer regions in mammalian chromosomes using silver staining

1 reference

12 December 2020

Identification of human chromosomes by DNA-binding fluorescent agents

1 reference

12 December 2020

3 CASES OF PARTIAL DELETION OF THE SHORT ARM OF A 5 CHROMOSOME

1 reference

12 December 2020

A simple technique for demonstrating centromeric heterochromatin

1 reference

12 December 2020

Identification of the abnormal B group chromosome in the "cri du chat" syndrome by QM-fluorescence

1 reference

12 December 2020

[Staining of human chromosomes with acridine orange after treatment with 5 bromodeoxyuridine]

1 reference

12 December 2020

A 45, XX,5–,13–, dic+ karyotype in a case of cri-du-chat syndrome

1 reference

12 December 2020

Autosomal deletions 46,XY,del(12)(p11) and 46,XY-46,XY,del(5)(p13) with no effect on physical or mental development.

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00283634

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:669700%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

12 September 2019

0 references

1 reference