Abstracts.
- Published in:
- Congenital Anomalies, 2023, v. 63, n. 6, p. A1, doi. 10.1111/cga.12546
- Publication type:
- Article
Works matching IS 09143505 AND DT 2023 AND VI 63 AND IP 6
Results: 12
1
2
Acknowledgments.
- Published in:
- Congenital Anomalies, 2023, v. 63, n. 6, p. 221, doi. 10.1111/cga.12545
- Publication type:
- Article
3
Efficacy of telepractice, an alternative therapy tool during the coronavirus disease 2019 pandemic, for speech disorders related to congenital anomalies.
- Published in:
- Congenital Anomalies, 2023, v. 63, n. 6, p. 206, doi. 10.1111/cga.12543
- By:
- Publication type:
- Article
4
Late diagnosis of Herlyn‐Werner‐Wunderlich syndrome: Is there a need for an early screening?
- Published in:
- Congenital Anomalies, 2023, v. 63, n. 6, p. 219, doi. 10.1111/cga.12542
- By:
- Publication type:
- Article
5
Survival rate of mice heterozygous for the dominant hemimelia mutation depends on the genetic background.
- Published in:
- Congenital Anomalies, 2023, v. 63, n. 6, p. 217, doi. 10.1111/cga.12541
- By:
- Publication type:
- Article
6
Recessive mutation on mouse chromosome 13 associated with abnormal hair texture and cardiomyopathy.
- Published in:
- Congenital Anomalies, 2023, v. 63, n. 6, p. 200, doi. 10.1111/cga.12540
- By:
- Publication type:
- Article
7
Orofacial clefts: Reflections on prenatal diagnosis and family history based on a series of cases of a tertiary children hospital.
- Published in:
- Congenital Anomalies, 2023, v. 63, n. 6, p. 195, doi. 10.1111/cga.12538
- By:
- Publication type:
- Article
8
Hypoalbuminemia in newborns with gastroschisis.
- Published in:
- Congenital Anomalies, 2023, v. 63, n. 6, p. 214, doi. 10.1111/cga.12537
- By:
- Publication type:
- Article
9
A variant in the LDL receptor‐related protein encoding gene LRP4 underlying polydactyly and phalangeal synostosis in a family of Pakistani origin.
- Published in:
- Congenital Anomalies, 2023, v. 63, n. 6, p. 190, doi. 10.1111/cga.12536
- By:
- Publication type:
- Article
10
First‐trimester prenatal diagnosis of Coffin‐Siris syndrome‐related congenital diaphragmatic hernia: The role of exome sequencing in determining genetic etiology.
- Published in:
- Congenital Anomalies, 2023, v. 63, n. 6, p. 211, doi. 10.1111/cga.12535
- By:
- Publication type:
- Article
11
An easy‐to‐use semi‐automatic volumetric evaluation for secondary bone grafting in patients with unilateral alveolar cleft.
- Published in:
- Congenital Anomalies, 2023, v. 63, n. 6, p. 182, doi. 10.1111/cga.12534
- By:
- Publication type:
- Article
12
Issue Information.
- Published in:
- Congenital Anomalies, 2023, v. 63, n. 6, p. 179, doi. 10.1111/cga.12479
- Publication type:
- Article