(Q35868297)

PubMed publication ID

10 August 2017

4 references

23 July 2020

13 August 2020

29 July 2022

Ethics of genetic counseling--basic concepts and relevance to Islamic communities (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6147893&resulttype=core&format=json

genetic predisposition to disease

12 May 2020

main subject

research ethics

0 references

2 references

23 July 2020

10 September 2020

cultural characteristic

1 reference

13 August 2020

Mohsen A F El-Hazmi

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6147893&resulttype=core&format=json

12 May 2020

publication date

1 March 2004

1 reference

PubMed publication ID

15323267

10 August 2017

published in

Annals of Saudi Medicine

4 references

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6147893&resulttype=core&format=json

12 May 2020

23 July 2020

13 August 2020

29 July 2022

24

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6147893&resulttype=core&format=json

12 May 2020

issue

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6147893&resulttype=core&format=json

12 May 2020

page(s)

84-92

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6147893&resulttype=core&format=json

Creative Commons Attribution-NonCommercial-NoDerivatives

12 May 2020

copyright license

4 references

23 July 2020

13 August 2020

10 September 2020

29 July 2022

Saudi aminoacidemias: a six-year study

1 reference

12 December 2020

Congenital abnormalities in newborns of consanguineous and nonconsanguineous parents

1 reference

12 December 2020

Sickle cell and G-6-PD deficiency gene in cord blood samples: experience at King Khalid University Hospital, Riyadh

1 reference

12 December 2020

Biotinidase deficiency: a treatable genetic disorder in the Saudi population.

1 reference

12 December 2020

Prevention of avoidable mutational disease: memorandum from a WHO meeting

1 reference

12 December 2020

Cystic fibrosis presenting with recurrent vomiting and metabolic alkalosis

1 reference

12 December 2020

Congenital hypothyroidism: Clinical and laboratory characteristics in infants detected by neonatal screening

1 reference

12 December 2020

X-linked adrenoleukodystrophy. The Saudi experience.

1 reference

12 December 2020

Early diagnosis of cystic fibrosis in Jordanian children

1 reference

12 December 2020

Ethical considerations in the prevention and management of genetic disorders with special emphasis on religious considerations.

1 reference

12 December 2020

Counselling about genetic disease: an Islamic perspective.

1 reference

12 December 2020

The demographics and distribution of type B Niemann-Pick disease: novel mutations lead to new genotype/phenotype correlations

1 reference

12 December 2020

10.5144/0256-4947.2004.84

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6147893&resulttype=core&format=json

12 May 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6147893&resulttype=core&format=json

12 May 2020

PubMed publication ID

15323267

1 reference