(Q33585957)

English

Craniorachischisis in a partially trisomic 11 fetus in a family with reproductive failure and a reciprocal translocation, t(6p plus;11q minus).

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Craniorachischisis in a partially trisomic 11 fetus in a family with reproductive failure and a reciprocal translocation, t(6p plus;11q minus). (English)

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

author name string

Wright YM

1

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Clark WE

2

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Breg WR

3

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

language of work or name

0 references

publication date

1 March 1974

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Journal of Medical Genetics

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

11

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

1

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

69-75

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

THE FREQUENCY OF MALDEVELOPMENT IN MAN: THE NEED FOR IMPROVED STATISTICS.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013090

21 June 2018

ANENECEPHALY IN FRANCE

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013090

21 June 2018

The inheritance of translocations in man: data from families ascertained through a balanced heterozygote

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013090

21 June 2018

Absent patellae, mild mental retardation, skeletal and genitourinary anomalies, and C group autosomal mosaicism.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013090

21 June 2018

Quinacrine fluorescent chromosome analysis of the Snell translocation in the mouse

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013090

21 June 2018

Quinacrine mustard fluorescence of human chromosomes: characterization of unusual translocations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013090

21 June 2018

Hypothesis: anencephaly and spina bifida are usually preventable by avoidance of a specific but unidentified substance present in certain potato tubers

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013090

21 June 2018

Four patients with trisomy 8 identified by the fluorescence and Giemsa banding techniques

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013090

21 June 2018

Mental retardation, absence of patellae, other malformations with chromosomal mosiacism.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013090

31 October 2018

An anencephalic male with XX sex chromosome complement

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013090

31 October 2018

Chromosome investigations of anencephaly and other congenital C.N.S. abnormalities in cork

1 reference

https://pubmed.ncbi.nlm.nih.gov/4134620

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Reciprocal translocations

1 reference

https://pubmed.ncbi.nlm.nih.gov/4134620

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Anencephaly in three siblings

1 reference

https://pubmed.ncbi.nlm.nih.gov/4134620

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Quinacrine fluorescence for identifying metaphase chromosomes, with special reference to photomicrography

1 reference

https://pubmed.ncbi.nlm.nih.gov/4134620

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

C 11-D 13-translocation in four generations

1 reference

https://pubmed.ncbi.nlm.nih.gov/4134620

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Experimental Induction of Foetal Malformation with “Blighted” Potato: a Preliminary Report

1 reference

https://pubmed.ncbi.nlm.nih.gov/4134620

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetics of anencephaly

1 reference

https://pubmed.ncbi.nlm.nih.gov/4134620

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Anencephaly in four consecutive pregnancies; report of a case

1 reference

https://pubmed.ncbi.nlm.nih.gov/4134620

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

FAMILIAL ANECEPHALY AND REARRANGEMENT OF 2 13-15 CHROMOSOMES

1 reference

https://pubmed.ncbi.nlm.nih.gov/4134620

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

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