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Association of prenatal Cleft Lip and Palate ultrasound abnormalities with copy number variants at a single Chinese tertiary center.

• Authors : Yan, Shujuan; Yu, Qiuxia; Zhou, Hang

Subjects: MEDICAL information storage & retrieval systems; STATISTICAL correlation; RESEARCH fundingCHINA

• Source: Italian Journal of Pediatrics; 8/21/2024, Vol. 50 Issue 1, p1-9, 9p

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Esophageal atresia in newborns: a wide spectrum from the isolated forms to a full VACTERL phenotype?

• Authors : Placa, Simona La; Giuffrè, Mario; Gangemi, Antonella

Subjects: ESOPHAGEAL atresia; TRACHEAL fistula; CLUSTER analysis (Statistics)ITALY

• Source: Italian Journal of Pediatrics; 2013, Vol. 39 Issue 1, p1-8, 8p, 1 Diagram, 3 Charts, 3 Graphs

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Congenital hypopituitarism and multiple midline defects in a newborn with non-familial Cat Eye syndrome.

• Authors : Serra, Gregorio; Giambrone, Clara; Antona, Vincenzo

Subjects: PHYSICAL diagnosis; HYPOPITUITARISM; CHOLESTASIS

• Source: Italian Journal of Pediatrics; 9/8/2022, Vol. 48 Issue 1, p1-8, 8p

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Recognizable neonatal clinical features of aplasia cutis congenita.

• Authors : Schierz, Ingrid Anne Mandy; Giuffrè, Mario; Del Vecchio, Antonello

Subjects: PERINATAL death; ACADEMIC medical centers; ANTHROPOMETRY

• Source: Italian Journal of Pediatrics; 2/18/2020, Vol. 46 Issue 1, p1-6, 6p

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Esophageal atresia in newborns: a wide spectrum from the isolated forms to a full VACTERL phenotype?

• Authors : La Placa, Simona; Giuffrè, Mario; Gangemi, Antonella

• Source: Italian Journal of Pediatrics. July 10, 2013, Vol. 39

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Chromosome 18q-syndrome and 1p terminal duplication in a patient with bilateral vesico-ureteral reflux: case report and literature revision.

• Authors : Brandigi E; Division of pediatric surgery, department of pediatrics, obstetrics and reproductive medicine, University of Siena, Siena, Italy. ; Molinaro F

Subjects: Abnormalities, Multiple/Abnormalities, Multiple/Abnormalities, Multiple/*genetics ; Chromosome Disorders/Chromosome Disorders/Chromosome Disorders/*genetics ; Chromosome Duplication/Chromosome Duplication/Chromosome Duplication/*genetics Chromosome 18 deletion syndrome

• Source: Italian journal of pediatrics [Ital J Pediatr] 2013 Jan 23; Vol. 39, pp. 6. Date of Electronic Publication: 2013 Jan 23.Publisher: BioMed Central Country of Publication: England NLM ID: 101510759 Publication Model: Electronic Cited Medium: Internet ISSN: 1824-7288

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