Found: 11
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Newborn with Anophthalmia and Features of Fryns Syndrome.
- Published in:
- Pediatric & Developmental Pathology, 2002, v. 5, n. 6, p. 592, doi. 10.1007/s10024-002-2106-2
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- Publication type:
- Article
Undifferentiated Embryonal Sarcoma with Unusual Features Arising within Mesenchymal Hamartoma of the Liver: Report of a Case and Review of the Literature.
- Published in:
- Pediatric & Developmental Pathology, 2001, v. 4, n. 5, p. 482, doi. 10.1007/s10024001-0047-9
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- Publication type:
- Article
Arthrogryposis and pterygia as lethal end manifestations of genetically defined congenital myopathies.
- Published in:
- American Journal of Medical Genetics. Part A, 2018, v. 176, n. 2, p. 359, doi. 10.1002/ajmg.a.38577
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- Publication type:
- Article
Solving an unusual case of acute kidney injury: Answers.
- Published in:
- Pediatric Nephrology, 2021, v. 36, n. 12, p. 4137, doi. 10.1007/s00467-021-05263-w
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- Publication type:
- Article
Solving an unusual case of acute kidney injury: Questions.
- Published in:
- 2021
- By:
- Publication type:
- Case Study
Endobronchial Glomus Tumor in a Child.
- Published in:
- Pediatric Allergy, Immunology & Pulmonology, 2019, v. 32, n. 4, p. 163, doi. 10.1089/ped.2019.1065
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- Publication type:
- Article
C1q nephropathy presenting as rapidly progressive crescentic glomerulonephritis.
- Published in:
- Pediatric Nephrology, 2000, v. 14, n. 10/11, p. 976, doi. 10.1007/s004670050056
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- Publication type:
- Article
Health Services Reforms in Revolutionary Nicaragua.
- Published in:
- American Journal of Public Health, 1984, v. 74, n. 10, p. 1138, doi. 10.2105/AJPH.74.10.1138
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- Publication type:
- Article
Loss of Function Variants in Human PNPLA8 Encoding Calcium-Independent Phospholipase A<sub>2</sub>γ Recapitulate the Mitochondriopathy of the Homologous Null Mouse.
- Published in:
- Human Mutation, 2015, v. 36, n. 6, p. 656, doi. 10.1002/humu.22790
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- Publication type:
- Article
Loss of Function Variants in Human PNPLA8 Encoding Calcium-Independent Phospholipase A<sub>2</sub>γ Recapitulate the Mitochondriopathy of the Homologous Null Mouse.
- Published in:
- Human Mutation, 2015, v. 36, n. 3, p. 301, doi. 10.1002/humu.22743
- By:
- Publication type:
- Article
Altered Pulmonary Lymphatic Development in Infants with Chronic Lung Disease.
- Published in:
- BioMed Research International, 2014, v. 2014, p. 1, doi. 10.1155/2014/109891
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- Publication type:
- Article