Familial café‐au‐lait macules associated with in‐frame deletion of NF1 p.Met992del mimicking Legius syndrome.
- Published in:
- Congenital Anomalies, 2023, v. 63, n. 2, p. 54, doi. 10.1111/cga.12506
- By:
- Publication type:
- Article
Works matching IS 09143505 AND DT 2023 AND VI 63 AND IP 2
Results: 7
1
2
Complementary mRNA expression of enzymes producing nitric oxide and prostaglandin in ductus arteriosus with respect to their role in maintaining patency.
- Published in:
- Congenital Anomalies, 2023, v. 63, n. 2, p. 47, doi. 10.1111/cga.12505
- By:
- Publication type:
- Article
3
Prenatal diagnosis of VACTERL association after early‐first trimester SARS‐COV‐2 infection.
- Published in:
- Congenital Anomalies, 2023, v. 63, n. 2, p. 44, doi. 10.1111/cga.12503
- By:
- Publication type:
- Article
4
Mouse vaginal development with lateral enlargement at late embryonic stages and caudal elongation after birth.
- Published in:
- Congenital Anomalies, 2023, v. 63, n. 2, p. 30, doi. 10.1111/cga.12502
- By:
- Publication type:
- Article
5
Late‐onset and congenital hearing loss detected using AABR due to congenital cytomegalovirus infection that improved with valganciclovir.
- Published in:
- Congenital Anomalies, 2023, v. 63, n. 2, p. 40, doi. 10.1111/cga.12501
- By:
- Publication type:
- Article
6
Vocal cord paralysis in autosomal dominant spinal muscular atrophy due to BICD2.
- Published in:
- Congenital Anomalies, 2023, v. 63, n. 2, p. 52, doi. 10.1111/cga.12500
- By:
- Publication type:
- Article
7
Issue Information.
- Published in:
- Congenital Anomalies, 2023, v. 63, n. 2, p. 27, doi. 10.1111/cga.12475
- Publication type:
- Article