Govaerts, L.C.

patient chromosome deletion mutation study analysis array syndrome result genet subject growth abnormality diagnosis region control fraxa table probe mosaicism igf 1r gene anomaly score ultrasound family omphalocele children level trisomy conditioning x syndrome netherland pregnancy experiment fetus outcome kidney phenotype group birth marker postnatal william disease number williams syndrome gh treatment treatment protein sample eyeblink tissue delay eyeblink conditioning parent identi fied igf-i percentage trisomy 17 mosaicism height factor trial igf 1r saving response delay cerebellar mosaic extinction savings experiment cytogenetic brain identi acquisition azoospermia gtf 2ird mutants erasmus mc genetic karyotype cancer marker chromosome