(Q50632435)

16 March 2018

title

Structural aberrations of chromosome 18. II. The 18q- syndrome. Report of three cases (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1112600

23 August 2022

main subject

human chromosomes 16-18

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1112600

23 August 2022

chromosome abnormality

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1112600

23 August 2022

author name string

A. Schinzel

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1112600

23 August 2022

K. Hayashi

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1112600

23 August 2022

W. Schmid

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1112600

23 August 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=1112600

23 August 2022

publication date

1 January 1975

1 reference

16 March 2018

published in

Humangenetik

1 reference

16 March 2018

volume

26

1 reference

16 March 2018

issue

2

1 reference

16 March 2018

page(s)

123-132

1 reference

16 March 2018

PARTIAL DELETION OF THE LONG ARMS OF THE CHROMOSOME 18

cites work

1 reference

12 December 2020

Clinical and chromosomal studies of the 18q-syndrome

1 reference

12 December 2020

Structural variation in human nitotic chromosomes

1 reference

12 December 2020

Familial occurrence of long arm deletion in chromosome 18 (46,18q-)

1 reference

12 December 2020

Familial 18 q- syndrome

1 reference

12 December 2020

The syndrome associated with the partial deletion of the long arms of chromosome 18 (18q-)

1 reference

12 December 2020

A case of 18q- in a family with a translocation t(6p+;18q-), identified by the Giemsa-banding technique

1 reference

12 December 2020

Partial deletion of long arms of chromosome 18

1 reference

12 December 2020

Chromosome 18 long arm deletion. A case with unusual dermatoglyphics

1 reference

12 December 2020

Ring chromosome 18. 18p-/18q- -deletion-syndrome

1 reference

12 December 2020

Partial deletion of the long arm of chromosome 18.

1 reference

12 December 2020

Two cases of 18q- syndrome with mosaicism (46,XX / 46,XX, 18q-)

1 reference

12 December 2020

(18q-) syndrome. A new finding on (46XX-46XX(18q-) mosaic

1 reference

12 December 2020

Partial deletion of the long arm of chromosome 18. Individualization of a new morbid state

1 reference

12 December 2020

Partial E-18 long-arm deletion

1 reference

12 December 2020

Identification of a D/E(15/18) translocation chromosome by quinacrine fluorescence and Urea banding techniques

1 reference

12 December 2020

Immunoglobulin abnormality in a girl with a large chromosome 18.

1 reference

12 December 2020

Multiple abnormalities due to possible genetic inactivation in an X-autosome translocation.

1 reference

12 December 2020

Deletion of chromosome 18

1 reference

12 December 2020

Partial deletion of the long arm of chromosome E-18

1 reference

12 December 2020

Structural aberrations of chromosome 18. I. The 18p-syndrome

1 reference

12 December 2020

[18 q- deletion. Case of mosaicism]

1 reference

12 December 2020

Deficiency on the long arm of a chromosome no. 18 (46,XX,18q-)

1 reference

12 December 2020

Cytogenetics in mentally defective children with anomalies: a controlled study

1 reference

12 December 2020

A case of 18q-syndrome

1 reference

12 December 2020

Absent IgA and deletions of chromosome 18

1 reference

12 December 2020

Structural abnormalities of chromosome 18. I. A case of 18q-, with autopsy findings

1 reference

12 December 2020

Gene deletion and duplication effects on phenotype and gamma globulin levels

1 reference

12 December 2020

A pedigree of 4/18 translocation chromosomes with type and countertype partial trisomy and partal monosomy for chromosome 18.

1 reference

12 December 2020

Syndrome associated with a deficiency of part of the long arm of chromosome no. 18

1 reference

12 December 2020

A case of 18q- in a t(18q-;6p+) family

1 reference

12 December 2020

Partial trisomy for the short arm of chromosome 4 with translocation 4p-,18q+ in the father

1 reference

12 December 2020

IgA deficiency associated with partial deletion of chromosome 18

1 reference

12 December 2020

The syndrome of 18th chromosomal long arm deletion

1 reference

12 December 2020

Deleted chromosome 18 with paternal mosaicism

1 reference

12 December 2020

A rapid banding technique for human chromosomes

1 reference

12 December 2020

The partial deletion of the long arm of chromosome 18 (syndrome 18Q-). Report of two cases

1 reference

12 December 2020

Deletion of the long arms of chromosome 18 (46,XX,18q-) associated with absence of IgA and hypothyroidism in an adult

1 reference

12 December 2020

Partial monosomy of the long arm of an E chromosome--a new syndrome

1 reference

12 December 2020

Aneusomie de recombinaison: rearrangement between paternal chromosomes 4 and 18 yielding offspring with features of the 18q- syndrome

1 reference

12 December 2020

Deficiency of the long arm of chromosome no. 18 (46,XX,18q-)

1 reference

12 December 2020

Identifiers

1 reference

16 March 2018