Predictive factors of iron depletion in late preterm infants at the postnatal age of 6 weeks von Akkermans, M D, Uijterschout, L, Abbink, M, Vos, P, Rövekamp-Abels, L, Boersma, B, van Goudoever, J B, Brus, F

Volltext

The influences of factors associated with decreased iron supply to the fetus during pregnancy on iron status in healthy children aged 0.5 to 3 years von Uijterschout, L, Vloemans, J, Rövekamp-Abels, L, Feitsma, H, van Goudoever, J B, Brus, F

Volltext

Modifier genes in Mendelian disorders: the example of cystic fibrosis von Cutting, Garry R.

Volltext

A transdisciplinary co‐conceptualisation of marine identity von Buchan, P. M., Glithero, L. D., McKinley, E., Strand, M., Champion, G., Kochalski, S., Velentza, K., Praptiwi, R. A., Jung, J., Márquez, M. C., Marra, M. V., Abels, L. M., Neilson, A. L., Spavieri, J., Whittey, K. E., Samuel, M. M., Hale, R., Čermák, A., Whyte, D., West, L., Stithou, M., Hegland, T. J., Morris‐Webb, E. S., Flander‐Putrle, V., Schiefer, P., Sutton, S., Onwubiko, C., Adeoye, O., Akpan, A., Payne, D. L.

Volltext

Congenital disorders of glycosylation von Jaeken, Jaak

Volltext

Disorders of dysregulated signal traffic through the RAS-MAPK pathway: phenotypic spectrum and molecular mechanisms von Tartaglia, Marco, Gelb, Bruce D.

Volltext

Life-threatening infectious diseases of childhood: single-gene inborn errors of immunity? von Alcaïs, Alexandre, Quintana-Murci, Lluis, Thaler, David S., Schurr, Erwin, Abel, Laurent, Casanova, Jean-Laurent

Volltext

Hearing loss: a common disorder caused by many rare alleles von Raviv, Dorith, Dror, Amiel A., Avraham, Karen B.

Volltext

Investigation of Mendelian forms of obesity holds out the prospect of personalized medicine von Blakemore, Alexandra I. F., Froguel, Philippe

Volltext

Modifier genes in Mendelian disorders: the example of hemoglobin disorders von Sankaran, Vijay G., Lettre, Guillaume, Orkin, Stuart H., Hirschhorn, Joel N.

Volltext

Hereditary kidney diseases: highlighting the importance of classical Mendelian phenotypes von Benoit, Geneviève, Machuca, Eduardo, Heidet, Laurence, Antignac, Corinne

Volltext

The role played by natural selection on Mendelian traits in humans von Quintana-Murci, Lluis, Barreiro, Luis B.

Volltext

Mendelian genetics of rare-and not so rare-cancers von Eng, Charis

Volltext

New insights in gene-derived therapy: the example of Duchenne muscular dystrophy von Aartsma-Rus, Annemieke, den Dunnen, Johan T., van Ommen, Gert-Jan B

Volltext

Clues to immune tolerance: the monogenic autoimmune syndromes von Waterfield, Michael, Anderson, Mark S.

Volltext

New Evidence of Long-lasting Persistence of Ebola Virus Genetic Material in Semen of Survivors von Sow, Mamadou S., Etard, Jean-François, Baize, Sylvain, Magassouba, N'Fally, Faye, Ousmane, Msellati, Philippe, Touré, Abdoulaye II, Savane, Ibrahima, Barry, Moumié, Delaporte, Eric

Volltext

Genetic regulation of human brain development: lessons from Mendelian diseases von Dixon-Salazar, Tracy J., Gleeson, Joseph G.

Volltext

Depressive symptoms among survivors of Ebola virus disease in Conakry (Guinea): preliminary results of the PostEboGui cohort von Keita, Mamady Mory, Taverne, Bernard, Sy Savané, Sékou, March, Laura, Doukoure, Morifodé, Sow, Mamadou Saliou, Touré, Abdoulaye, Etard, Jean François, Barry, Moumié, Delaporte, Eric

Volltext

Disruption of long-distance highly conserved noncoding elements in neurocristopathies von Amiel, Jeanne, Benko, Sabina, Gordon, Christopher T., Lyonnet, Stanislas

Volltext

Impact of Mendelian inheritance in cardiovascular disease von McBride, Kim L., Garg, Vidu

Volltext