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Tracy Hampton, PhD, MDLinx Oncology

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Haploinsufficiency at GCK gene is not a frequent event in MODY2 patients
Clinical Endocrinology, 05/19/08

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Free Abstract

Garin I et al. - Strict maternal euglycaemia can contribute to intrauterine growth restriction and low BW when the foetus has inherited the GCK mutation from the mother. As foetal genotype in generally is not known, serial foetal abdominal scans may act as a surrogate for this.

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