(Q53749365)

19 May 2018

title

Chromosome analysis before birth and its value in genetic counselling. (English)

1 reference

19 May 2018

author name string

Ferguson-Smith ME

1

1 reference

19 May 2018

Ferguson-Smith MA

2

1 reference

19 May 2018

Nevin NC

3

1 reference

19 May 2018

Stone M

4

1 reference

19 May 2018

language of work or name

English

0 references

publication date

1 October 1971

1 reference

19 May 2018

published in

The BMJ

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19 May 2018

volume

4

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19 May 2018

issue

5779

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19 May 2018

page(s)

69-74

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19 May 2018

The use of amniocentesis for prenatal genetic counseling

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1799312

Technique for identifying Y chromosomes in human interphase nuclei.

19 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1799312

Prenatal diagnosis of Tay-Sachs disease.

19 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1799312

Biochemical diagnosis of an X-linked disease in utero.

19 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1799312

Fatal granulomatous disease of childhood and benign lymphocytic infiltration of the skin (congenital dysphagocytosis).

19 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1799312

Hurler's syndrome. A genetic study in cell culture

19 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1799312

Quinacrine fluorescence of the human Y chromosome.

19 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1799312

Amniotic fluid cells; prenatal sex prediction and culture.

19 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1799312

Polyploidy in cells cultured from amniotic fluid

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1799312

Prenatal detection of genetic defects

13 August 2018

1 reference

12 December 2020

Y-fluorescence of interphase nuclei, especially circulating lymphocytes

1 reference

12 December 2020

CHROMOSOME STUDIES IN SPONTANEOUS ABORTIONS

1 reference

12 December 2020

Diagnosis of the adrenogenital syndrome before birth

1 reference

12 December 2020

1 reference

12 December 2020

Amniocentesis in genetic counseling. Safety and reliability in early pregnancy

1 reference

12 December 2020

Prenatal determination of fetal sex and chromosomal complement

1 reference

12 December 2020

Cytology of amniotic fluid

1 reference

12 December 2020

Antenatal detection of chromosome abnormalities

1 reference

12 December 2020

Antenatal detection of partial C (6-12) trisomy

1 reference

12 December 2020

Intrauterine diagnosis of the hurler and hunter syndromes

1 reference

12 December 2020

Culture of cells obtained by amniocentesis

1 reference

12 December 2020

Antenatal detection of hereditary disorders

1 reference

12 December 2020

Role of amniocentesis in the intrauterine detection of genetic disorders

1 reference

12 December 2020

Cytologic study of amniotic fluid in pregnancy

1 reference

12 December 2020

Intrauterine diagnosis and management of genetic defects

1 reference

12 December 2020

Identifiers

DOI

10.1136/BMJ.4.5779.69

1 reference

19 May 2018

PMCID

1799312

1 reference

19 May 2018

PubMed ID

4255487

1 reference

19 May 2018