Familial mental retardation in a family with an inherited chromosome rearrangement. (Q33586281)

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8 October 2019

title

Familial mental retardation in a family with an inherited chromosome rearrangement (English)

1 reference

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8 October 2019

author name string

A E Chudley

1

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8 October 2019

F Bauder

2

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8 October 2019

M Ray

3

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8 October 2019

P J McAlpine

4

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8 October 2019

S D Pena

5

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8 October 2019

J L Hamerton

6

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8 October 2019

publication date

1 December 1974

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Journal of Medical Genetics

8 October 2019

language of work or name

English

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published in

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8 October 2019

volume

11

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8 October 2019

issue

4

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8 October 2019

page(s)

353-366

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CHROMOSOME 18: A TOPOLOGIC APPROACH.

8 October 2019

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013205

Absent IgA and deletions of chromosome 18

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013205

Immunological profile in a chromosome 18 deletion syndrome with IgA deficiency

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013205

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013205

Probable assignment of the Duffy blood group locus to chromosome 1 in man

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013205

Gene deletion and duplication effects on phenotype and gamma globulin levels

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013205

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013205

Assignment of the genes for human peptidase A to chromosome 18 and cytoplasmic glutamic oxaloacetate transaminase to chromosome 10 using somatic-cell hybrids

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013205

Partial monosomies 18. Review of cytogenetical and phenotypical variants

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013205

Assignment by Deletion of Human Red Cell Acid Phosphatase Gene Locus to the Short Arm of Chromosome 2

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013205

A cytogenetic survey of 11,680 newborn infants

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013205

IgA and partial deletions of chromosome 18.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013205

An analysis of the break points of structural rearrangements in man

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013205

Common polymorphism of Peptidase A. Electrophoretic variants associated with quantitative variation of red cell levels

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013205

IgA deficiency associated with partial deletion of chromosome 18

31 October 2018

1 reference

12 December 2020

Asymmetry of chromosome number 1 pair in three generations of a phenotypically normal family

1 reference

12 December 2020

Probable Assignment of the Alpha Locus of Haptoglobin to Chromosome 16 in Man

1 reference

12 December 2020

Differential binding of alkylating fluorochromes in human chromosomes

1 reference

12 December 2020

Heritable Fragile Site on Chromosome 16: Probable Localization of Haptoglobin Locus in Man

1 reference

12 December 2020

Clinical and chromosomal studies of the 18q-syndrome

1 reference

12 December 2020

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

1 reference

12 December 2020

New technique for distinguishing between human chromosomes

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

A rapid banding technique for human chromosomes

1 reference

12 December 2020

Banding in human chromosomes treated with trypsin

1 reference

12 December 2020

An interstitial translocation: chromosome no. 1p to 4q

1 reference

12 December 2020

Familial insertional translocation

1 reference

12 December 2020

Interstitial translocation in man

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12 December 2020

Trisomy for the distal part of the short arm of the number 3 chromosome in 3 siblings. First example of chromosomal insertion: INS(7;3)(q 31;p 21 p 26)

1 reference

12 December 2020

Linkage Analysis in Man by Somatic Cell Genetics

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

Localization of the Structural Gene for Human Peptidase-A to Chromosome 18

1 reference

12 December 2020

PARTIAL DELETION OF THE LONG ARMS OF THE CHROMOSOME 18

1 reference

12 December 2020

Identifiers

DOI

10.1136/JMG.11.4.353

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4140909%20AND%20SRC:MED&resulttype=core&format=json

8 October 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4140909%20AND%20SRC:MED&resulttype=core&format=json

8 October 2019

PubMed publication ID

4140909

1 reference