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  • About
  • The Global ETD Search service is a free service for researchers to find electronic theses and dissertations. This service is provided by the Networked Digital Library of Theses and Dissertations.
    Our metadata is collected from universities around the world. If you manage a university/consortium/country archive and want to be added, details can be found on the NDLTD website.
41

Capturing epigenomes at high-resolution for insight into genome function and metabolic disease risk

Allum-Bordage, Fiona Vanessa January 2019 (has links)
No description available.
42

Interpretation of maternal and fetal biomarkers in a population with coexisting nutrient deficiencies and infections

Gonzalez, Doris January 2019 (has links)
No description available.
43

The influence of sports, energy, vitamin D and calcium intake on bone mineral density in female athletic and sedentary students

De la Parra Sólomon, Adriana January 2019 (has links)
No description available.
44

Validity of a screening survey tool to identify neonates at high risk for vitamin D deficiency

Patel, Sharina January 2019 (has links)
No description available.
45

Dopamine receptor D2 (DRD2) antagonism as a therapeutic approach against pancreatic cancer

Bakadlag, Rowa January 2019 (has links)
No description available.
46

Bringing the genetics of osteoporosis to the clinic

Keller-Baruch, Julyan January 2019 (has links)
No description available.
47

Determinants of small-for-gestational-age: a case study in a conflict-zone in Colombia

Sahajpal, Revathi January 2020 (has links)
No description available.
48

An autosomal recessive alopecia areata locus with lymphoproliferative syndrome in mice

Alshareef, Maryam January 2015 (has links)
No description available.
49

The biological importance and mechanisms of long-chain polyunsaturated fatty acids on bone growth in diet-induced obesity: Investigation in children with obesity and rodents

Mak, Ivy January 2020 (has links)
No description available.
50

SCARF2 and SNAP29: candidate genes implicated in the generation of phenotypic variability in 22q11.2 deletion syndrome

Keser, Vafa January 2019 (has links)
No description available.

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