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Search Results to Yuri Zarate

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One or more keywords matched the following items that are connected to Zarate, Yuri

Item TypeName
Academic Article Evaluation of growth in patients with isolated cleft lip and/or cleft palate.
Academic Article Genetic causes of macroglossia: diagnostic approach.
Academic Article Lethal presentation of neurofibromatosis and Noonan syndrome.
Academic Article Novel fibrillin 1 mutation in a case of neonatal Marfan syndrome: the increasing importance of early recognition.
Concept Respiratory Distress Syndrome, Newborn
Concept Infant, Newborn
Academic Article Severe neonatal presentation of Kleefstra syndrome in a patient with hypoplastic left heart syndrome and 9q34.3 microdeletion.
Academic Article Persistent congenital hyperinsulinism in two patients with Beckwith-Wiedemann syndrome due to mosaic uniparental disomy 11p.
Academic Article Radioulnar Synostosis and Brain Abnormalities in a Patient With 17q21.31 Microdeletion Involving EFTUD2.
Academic Article Impact of aortic aneurysm on hospitalizations in patients with marfan syndrome: a multi-institutional study.
Academic Article Molecular and cytogenetic evaluation of a patient with ring chromosome 13 and discordant results.
Academic Article STAR syndrome is part of the differential diagnosis of females with anorectal malformations.
Academic Article Phenotypic modifications of patients with full chromosome aneuploidies and concurrent suspected or confirmed second diagnoses.
Academic Article Aortic dilation in pediatric patients.
Academic Article First clinical report of an infant with microcephaly and CASC5 mutations.
Academic Article Arterial tortuosity syndrome: 40 new families and literature review.
Academic Article Combined Tongue-Palate Fusion With Alveolar Bands in a Patient With Pierre Robin Sequence and Van der Woude Syndrome.
Academic Article Frequency and age at occurrence of clinical manifestations of disease in patients with hypophosphatasia: a systematic literature review.
Academic Article Nuclear radiation and prevalence of structural birth defects among infants born to women from the Marshall Islands.
Academic Article Genetic variants in DGAT1 cause diverse clinical presentations of malnutrition through a specific molecular mechanism.

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  • Infant Newborn