Found: 9
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Multiple craniosynostosis and facial dysmorphisms with homozygous IL11RA variant caused by maternal uniparental isodisomy of chromosome 9.
- Published in:
- Congenital Anomalies, 2020, v. 60, n. 5, p. 153, doi. 10.1111/cga.12371
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- Article
Announcement.
- Published in:
- Congenital Anomalies, 2020, v. 60, n. 5, p. 158, doi. 10.1111/cga.12390
- Publication type:
- Article
Neurofibromatosis type 1 due to possible maternal mosaicism in a family with two affected siblings.
- Published in:
- Congenital Anomalies, 2020, v. 60, n. 5, p. 156, doi. 10.1111/cga.12373
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- Article
Infant with trisomy 13 who developed acute elevation of intraocular pressure and glaucoma.
- Published in:
- Congenital Anomalies, 2020, v. 60, n. 5, p. 151, doi. 10.1111/cga.12367
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- Article
Maternal administration of bisphenol A alters the microglial profile in the neocortex of mouse weanlings.
- Published in:
- Congenital Anomalies, 2020, v. 60, n. 5, p. 142, doi. 10.1111/cga.12370
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- Article
Variants in NIPAL4 and ALOXE3 cause autosomal recessive congenital ichthyosis in Pakistani families.
- Published in:
- Congenital Anomalies, 2020, v. 60, n. 5, p. 149, doi. 10.1111/cga.12366
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- Article
5‐Aminolevulinic acid can ameliorate language dysfunction of patients with ATR‐X syndrome.
- Published in:
- Congenital Anomalies, 2020, v. 60, n. 5, p. 147, doi. 10.1111/cga.12365
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- Publication type:
- Article
Amniotic fluid levels of selected trace elements and heavy metals in pregnancies complicated with neural tube defects.
- Published in:
- Congenital Anomalies, 2020, v. 60, n. 5, p. 136, doi. 10.1111/cga.12363
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- Publication type:
- Article
Issue Information.
- Published in:
- Congenital Anomalies, 2020, v. 60, n. 5, p. 133, doi. 10.1111/cga.12344
- Publication type:
- Article