Found: 7
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A novel large in-frame FBN1 deletion causes neonatal Marfan syndrome.
- Published in:
- Cold Spring Harbor Molecular Case Studies, 2022, v. 8, n. 6, p. 1, doi. 10.1101/mcs.a006213
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- Publication type:
- Article
Array-based molecular karyotyping in 115 VATER/VACTERL and VATER/VACTERL-like patients identifies disease-causing copy number variations.
- Published in:
- Birth Defects Research, 2017, v. 109, p. 1063, doi. 10.1002/bdr2.1042
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- Publication type:
- Article
Array-based molecular karyotyping in 115 VATER/VACTERL and VATER/VACTERL-like patients identifies disease-causing copy number variations.
- Published in:
- Birth Defects Research, 2017, v. 109, n. 13, p. 1063, doi. 10.1002/bdr2.1042
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- Publication type:
- Article
Human herpes virus-6 DNA in cerebrospinal fluid of children undergoing therapy for acute leukaemia.
- Published in:
- 2009
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- Publication type:
- Letter
Epidemiology and One-Year Follow-Up of Neonates with CDH-Data from Health Insurance Claims in Germany.
- Published in:
- Children, 2021, v. 8, n. 2, p. 1, doi. 10.3390/children8020160
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- Publication type:
- Article
Treatment of fetomaternal neonatal alloimmune thrombocytopenia with random platelets.
- Published in:
- Pediatric Blood & Cancer, 2008, v. 50, n. 6, p. 1293, doi. 10.1002/pbc.21531
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- Publication type:
- Article
Case Report: Symptomatic Chronic Granulomatous Disease in the Newborn.
- Published in:
- Frontiers in Immunology, 2021, v. 11, p. N.PAG, doi. 10.3389/fimmu.2021.663883
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- Publication type:
- Article