957 research outputs found
Radical hysterectomy alone or combined with neoadjuvant chemotherapy in the treatment of early stage bulky cervical carcinoma
Rapid genetic analysis of oculocutaneous albinism (OCA1) using denaturing high performance liquid chromatography (DHPLC) system
Prenatal two- and three-dimensional ultrasound diagnosis of limb reduction defects associated with homozygous alpha-thalassemia
Asymmetrical terminal limb defects in a hydropic infant with homozygous alpha-thalassemia-1
Novel mutation in the TSC2 gene associated with prenatally diagnosed cardiac rhabdomyomas and cerebral tuberous sclerosis
c-Myc directly regulates the transcription of the NBS1 gene involved in DNA double-strand break repair.
PHOX2B Mutation-Confirmed Congenital Central Hypoventilation Syndrome in a Chinese Family.
Favourable outcome in a pregnancy with concomitant maternal and fetal osteogenesis imperfecta associated with a novel COL1A2 mutation
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