Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Ujala Aymun"'
Publikováno v:
Biomedical Papers, Vol 161, Iss 2, Pp 158-163 (2017)
Background: Fanconi anemia is a rare autosomal recessive disorder of genetic instability. It is both molecularly and clinically, a heterogeneous disorder. Its incidence is 1 in 129,000 births and relatively high in some ethnic groups. Sixteen genes h
Externí odkaz:
https://doaj.org/article/a1bd360f7c17415fa5255b0f1a864892
Publikováno v:
Pakistan Journal of Medical and Health Sciences. 17:593-595
Introduction: Iron is the most prevalent nutrient deficiency in infants and young children around the world despite its importance for healthy brain development. Infants who drink whole cow's milk or other animal milks are at a greater risk of develo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1ed99255bc52395705aaa601403c2dc6
https://doi.org/10.53350/pjmhs2023172593
https://doi.org/10.53350/pjmhs2023172593
Publikováno v:
Biomedical Papers, Vol 161, Iss 2, Pp 158-163 (2017)
Background: Fanconi anemia is a rare autosomal recessive disorder of genetic instability. It is both molecularly and clinically, a heterogeneous disorder. Its incidence is 1 in 129,000 births and relatively high in some ethnic groups. Sixteen genes h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::515160c57999043a9b8702ee65288da9
https://biomed.papers.upol.cz/artkey/bio-201702-0006_Screening_for_mutations_in_two_exons_of_FANCG_gene_in_Pakistani_population.php
https://biomed.papers.upol.cz/artkey/bio-201702-0006_Screening_for_mutations_in_two_exons_of_FANCG_gene_in_Pakistani_population.php