(Q43433254)

English

A 46,XY, del(18)(pter leads to p1 100:) cebocephalic child from a 46,XX,t(12;18)(18pter leads to 18 p 1100:: 12qter leads to 12pter) normal parent

scientific article published on September 10, 1976

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

23 November 2017

A 46,XY, del(18)(pter leads to p1 100:) cebocephalic child from a 46,XX,t(12;18)(18pter leads to 18 p 1100:: 12qter leads to 12pter) normal parent (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A964998

10 August 2022

human chromosomes 6-12 and X

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A964998

10 August 2022

human chromosomes 16-18

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A964998

10 August 2022

chromosome abnormality

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A964998

10 August 2022

chromosomal deletion syndrome

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A964998

10 August 2022

author name string

G. Johnson

1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A964998

10 August 2022

R. Bachman

2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A964998

10 August 2022

language of work or name

1 reference

based on heuristic

inferred from title

publication date

1 September 1976

1 reference

Europe PubMed Central

PubMed publication ID

23 November 2017

10 September 1976

1 reference

National Center for Biotechnology Information

PubMed publication ID

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=964998

10 August 2022

1 reference

Europe PubMed Central

PubMed publication ID

23 November 2017

34

1 reference

Europe PubMed Central

PubMed publication ID

23 November 2017

1

1 reference

Europe PubMed Central

PubMed publication ID

23 November 2017

103-106

1 reference

Europe PubMed Central

PubMed publication ID

23 November 2017

https://scigraph.springernature.com/pub.10.1007/bf00284446

0 references

An 18p21q Translocation in a Patient With Presumptive "Monosomy G"

1 reference

https://pubmed.ncbi.nlm.nih.gov/964998

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

New technique for distinguishing between human chromosomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/964998

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of a 18-21 translocation with Klinefelter's syndrome by G-band patterns

1 reference

https://pubmed.ncbi.nlm.nih.gov/964998

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

FAMILIAL SHORT ARM DEFICIENCY OF CHROMOSOME 18 CONCOMITANT WITH ARHINENCEPHALY AND ALOPECIA CONGENITA

1 reference

https://pubmed.ncbi.nlm.nih.gov/964998

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Complete deletion of the short arm of chromosome 18 and G-18 translocation with dyschromy and hypothyroidism

1 reference

https://pubmed.ncbi.nlm.nih.gov/964998

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dicentric chromosome due to an unusual fusion

1 reference

https://pubmed.ncbi.nlm.nih.gov/964998

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Arrhinencephaly associated with a deficiency involving chromosome 18

1 reference

https://pubmed.ncbi.nlm.nih.gov/964998

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

On a case of partial deletion of the short arm of chromosome 18, resulting in a familial 18c-17 translocation

1 reference

https://pubmed.ncbi.nlm.nih.gov/964998

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The use of proteolytic enzymes for the mapping of structural rearrangements in the chromosomes of man

1 reference

https://pubmed.ncbi.nlm.nih.gov/964998

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The 24 fluorescence patterns of the human metaphase chromosomes - distinguishing characters and variability

1 reference

https://pubmed.ncbi.nlm.nih.gov/964998

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00284446

1 reference

Europe PubMed Central

PubMed publication ID

23 November 2017

Dimensions Publication ID

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

23 November 2017

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