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- Cumulative risk factors contributing to hearing loss in preterm infantsKathy Chant, Maria Bitner-Glindzicz, Neil MarlowArchives of Disease in Childhood - Fetal and Neonatal Edition Sep 2023, 108 (5) 464-470; DOI: 10.1136/archdischild-2022-324331
- Newborn with isolated severe deficiency of cranial vault ossification: a case of cleidocranial dysplasiaElena Borelli, Salvatore Aversa, Mario Motta, Elisa Cavalleri, Claudio Cereda, Lorenzo Pinelli, Alba Pilotta, Francesco Maria RissoArchives of Disease in Childhood - Fetal and Neonatal Edition Jul 2023, fetalneonatal-2023-325794; DOI: 10.1136/archdischild-2023-325794
- Unusual position of the umbilicus in a neonateShu Ki Tsoi, Catherine Brock, Marcelle Simeonovic, Thao Lu, Niranjan ThomasArchives of Disease in Childhood - Fetal and Neonatal Edition Jan 2022, 107 (1) 94; DOI: 10.1136/archdischild-2020-321003
- Phenotypic and genetic spectrum of alveolar capillary dysplasia: a retrospective cohort studyLaurélia Jourdan-Voyen, Renaud Touraine, Jean-Pierre Masutti, Tiffany Busa, Catherine Vincent-Delorme, Lelia Dreyfus, Arnaud Molin, Baptiste Savey, Abraham Mounzer, Ziad Assaf, Veronique Atallah, Vanessa da Cruz, Dominique Gaillard, Elise Leroy-Terquem, Jean-Baptiste Mouton, Jamal Ghoumid, Jean-Charles Picaud, Frederique Dijoud, Sonia Bouquillon, Cédric Baumann, Laetitia LambertArchives of Disease in Childhood - Fetal and Neonatal Edition Jul 2020, 105 (4) 387-392; DOI: 10.1136/archdischild-2019-317121
- Desmoid tumour: rare presentation following neonatal lumbar punctureEmily Anderson, Caren Landes, Emma McCannArchives of Disease in Childhood - Fetal and Neonatal Edition May 2020, 105 (3) 298; DOI: 10.1136/archdischild-2018-316210
- Genetic background of high blood pressure is associated with reduced mortality in premature neonatesWolfgang Göpel, Mirja Müller, Heike Rabe, Johannes Borgmann, Tanja K Rausch, Kirstin Faust, Angela Kribs, Jörg Dötsch, David Ellinghaus, Christoph Härtel, Claudia Roll, Miklos Szabo, Peter Nürnberg, Andre Franke, Inke R König, Mark A Turner, Egbert HertingArchives of Disease in Childhood - Fetal and Neonatal Edition Mar 2020, 105 (2) 184-189; DOI: 10.1136/archdischild-2019-317131
- Extending non-invasive prenatal testing to non-invasive prenatal diagnosisRachel Helen Horton, Diana Gay WellesleyArchives of Disease in Childhood - Fetal and Neonatal Edition Jan 2019, 104 (1) F6-F7; DOI: 10.1136/archdischild-2018-314845
- Highlights from the literatureArchives of Disease in Childhood - Fetal and Neonatal Edition Jan 2018, 103 (1) F90; DOI: 10.1136/archdischild-2017-314461
- Genome-wide association study of sepsis in extremely premature infantsLakshmi Srinivasan, Grier Page, Haresh Kirpalani, Jeffrey C Murray, Abhik Das, Rosemary D Higgins, Waldemar A Carlo, Edward F Bell, Ronald N Goldberg, Kurt Schibler, Beena G Sood, David K Stevenson, Barbara J Stoll, Krisa P Van Meurs, Karen J Johnson, Joshua Levy, Scott A McDonald, Kristin M Zaterka-Baxter, Kathleen A Kennedy, Pablo J Sánchez, Shahnaz Duara, Michele C Walsh, Seetha Shankaran, James L Wynn, C Michael CottenArchives of Disease in Childhood - Fetal and Neonatal Edition Sep 2017, 102 (5) F439-F445; DOI: 10.1136/archdischild-2016-311545
- The outcome of prenatal identification of sex chromosome abnormalitiesAngela K Lucas-Herald, Fiona Cann, Lorna Crawford, Holly Morrison, Massoud Boroujerdi, Scott M Nelson, S Faisal Ahmed, Ruth McGowanArchives of Disease in Childhood - Fetal and Neonatal Edition Sep 2016, 101 (5) F423-F427; DOI: 10.1136/archdischild-2015-309681
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