Announcement.
- Published in:
- Congenital Anomalies, 2019, v. 59, n. 1, p. 28, doi. 10.1111/cga.12321
- Publication type:
- Article
Works matching IS 09143505 AND DT 2019 AND VI 59 AND IP 1
Results: 8
1
2
Issue Information.
- Published in:
- Congenital Anomalies, 2019, v. 59, n. 1, p. 1, doi. 10.1111/cga.12295
- Publication type:
- Article
3
Further evidence for causation of ischiospinal dysostosis by a pathogenic variant in BMPER and expansion of the phenotype.
- Published in:
- Congenital Anomalies, 2019, v. 59, n. 1, p. 26, doi. 10.1111/cga.12285
- By:
- Publication type:
- Article
4
Investigation of maxillofacial morphology and oral characteristics with Turner syndrome and early mixed dentition.
- Published in:
- Congenital Anomalies, 2019, v. 59, n. 1, p. 11, doi. 10.1111/cga.12284
- By:
- Publication type:
- Article
5
Morphological development of baculum and forelimb second‐to‐fourth digit ratio in mice.
- Published in:
- Congenital Anomalies, 2019, v. 59, n. 1, p. 24, doi. 10.1111/cga.12283
- By:
- Publication type:
- Article
6
XPC gene mutations in families with xeroderma pigmentosum from Pakistan; prevalent founder effect.
- Published in:
- Congenital Anomalies, 2019, v. 59, n. 1, p. 18, doi. 10.1111/cga.12281
- By:
- Publication type:
- Article
7
Spinal muscular atrophy with respiratory distress type 1 associated with novel compound heterozygous mutations in IGHMBP2: Differential diagnosis in a case with congenital diaphragm eventration.
- Published in:
- Congenital Anomalies, 2019, v. 59, n. 1, p. 22, doi. 10.1111/cga.12280
- By:
- Publication type:
- Article
8
Multiplex PCR in noninvasive prenatal diagnosis for FGFR3‐related disorders.
- Published in:
- Congenital Anomalies, 2019, v. 59, n. 1, p. 4, doi. 10.1111/cga.12278
- By:
- Publication type:
- Article