(Q35199102)

7 August 2017

Prenatal diagnosis of sickle hemoglobinopathies: the experience of the Columbia University Comprehensive Center for Sickle Cell Disease (English)

1 reference

7 August 2017

0 references

M C Driscoll

1

1 reference

7 August 2017

N Lerner

2

1 reference

7 August 2017

K Anyane-Yeboa

3

1 reference

7 August 2017

J Maidman

4

1 reference

7 August 2017

D Warburton

5

1 reference

7 August 2017

K Schaefer-Rego

6

1 reference

7 August 2017

R Hsu

7

1 reference

7 August 2017

C Ince

8

1 reference

7 August 2017

J Malin

9

1 reference

7 August 2017

M Pallai

10

1 reference

7 August 2017

language of work or name

English

0 references

publication date

1 June 1987

1 reference

American Journal of Human Genetics

7 August 2017

1 reference

7 August 2017

40

1 reference

7 August 2017

6

1 reference

7 August 2017

548-558

1 reference

Prevention of homozygous beta-thalassemia by carrier screening and prenatal diagnosis in Sardinia.

7 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684158

Direct detection of the common Mediterranean beta-thalassemia gene with synthetic DNA probes. An alternative approach for prenatal diagnosis

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684158

Beta-thalassemia disease prevention: genetic medicine applied.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684158

Direct identification of sickle cell anemia by blot hybridization

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684158

A nucleotide change at a splice junction in the human beta-globin gene is associated with beta 0-thalassemia

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684158

Effect of fetal diagnostic testing on birth-rate of thalassaemia major in Britain

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684158

The mutation and polymorphism of the human beta-globin gene and its surrounding DNA.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684158

In utero diagnosis of hemoglobinopathies. Technic for obtaining fetal blood.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684158

Antenatal diagnosis of thalassemia: a review

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684158

Hematologically and genetically distinct forms of sickle cell anemia in Africa. The Senegal type and the Benin type

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684158

Polymorphism of DNA sequence adjacent to human beta-globin structural gene: relationship to sickle mutation

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684158

Changes in restricted human cellular DNA fragments containing globin gene sequences in thalassemias and related disorders

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684158

Current sickle cell screening program for newborns in New York City, 1979-1980.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684158

Absence of maternal contamination of chorionic villi used for fetal-gene analysis

26 September 2018

1 reference

12 December 2020

A high incidence of maternal cell contamination of amniotic fluid cell cultures

1 reference

12 December 2020

Prenatal Diagnosis of Sickle-Cell Anemia in the First Trimester of Pregnancy

1 reference

12 December 2020

Error in prenatal diagnosis by DNA analysis

1 reference

12 December 2020

Highly sensitive and rapid gene mapping using miniaturized blot hybridization: application to prenatal diagnosis

1 reference

12 December 2020

Prenatal diagnosis of thalassemia and Hb S syndromes in Greece: an evaluation of 1500 cases

1 reference

12 December 2020

Successful Application of Prenatal Diagnosis in a Pregnancy at Risk for Homozygous β-Thalassemia

1 reference

12 December 2020

Prevention of thalassaemia in Cyprus

1 reference

12 December 2020

A Sensitive New Prenatal Test for Sickle-Cell Anemia

1 reference

12 December 2020

Improved detection of the sickle mutation by DNA analysis: application to prenatal diagnosis

1 reference

12 December 2020

Prenatal diagnosis using DNA polymorphisms. Report on 95 pregnancies at risk for sickle-cell disease or beta-thalassemia

1 reference

12 December 2020

Prenatal diagnosis of beta-thalassemia. Detection of a single nucleotide mutation in DNA

1 reference

12 December 2020

Identifiers

PMCID

1684158

1 reference

7 August 2017

1 reference