Works matching IS 09143505 AND DT 2019 AND VI 59 AND IP 3
Results: 9
Announcement.
- Published in:
- Congenital Anomalies, 2019, v. 59, n. 3, p. 104, doi. 10.1111/cga.12338
- Publication type:
- Article
Molecular mechanisms underlying the models of neurodevelopmental disorders in maternal immune activation relevant to the placenta.
- Published in:
- Congenital Anomalies, 2019, v. 59, n. 3, p. 81, doi. 10.1111/cga.12323
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- Publication type:
- Article
Developmental mutant mouse models for external genitalia formation.
- Published in:
- Congenital Anomalies, 2019, v. 59, n. 3, p. 74, doi. 10.1111/cga.12319
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- Publication type:
- Article
Congenital eye anomalies: More mosaic than thought?
- Published in:
- Congenital Anomalies, 2019, v. 59, n. 3, p. 56, doi. 10.1111/cga.12304
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- Publication type:
- Article
Identification and association of recurrent ALOXE3 mutation with non‐bullous congenital ichthyosiform erythroderma in two ethnically distinct Pakistani families.
- Published in:
- Congenital Anomalies, 2019, v. 59, n. 3, p. 93, doi. 10.1111/cga.12303
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- Publication type:
- Article
Potentially effective method for fetal gender determination by noninvasive prenatal testing for X‐linked disease.
- Published in:
- Congenital Anomalies, 2019, v. 59, n. 3, p. 88, doi. 10.1111/cga.12302
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- Publication type:
- Article
Long‐term natural history of an adult patient with distal 22q11.2 deletion from low copy repeat‐D to E.
- Published in:
- Congenital Anomalies, 2019, v. 59, n. 3, p. 102, doi. 10.1111/cga.12301
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- Publication type:
- Article
Issue Information.
- Published in:
- Congenital Anomalies, 2019, v. 59, n. 3, p. 53, doi. 10.1111/cga.12297
- Publication type:
- Article
Novel compound heterozygous and homozygous variants of laminin subunit β3 gene underlie non‐Herlitz junctional epidermolysis bullosa in two paternal half‐brothers from Saudi Arabia.
- Published in:
- Congenital Anomalies, 2019, v. 59, n. 3, p. 99, doi. 10.1111/cga.12294
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- Publication type:
- Article