Early prenatal detection of short‐rib polydactyly syndrome in a monochorionic diamniotic twin pregnancy.
- Published in:
- Congenital Anomalies, 2019, v. 59, n. 5, p. 181, doi. 10.1111/cga.12317
- By:
- Publication type:
- Article
Works matching IS 09143505 AND DT 2019 AND VI 59 AND IP 5
Results: 7
1
2
Mutational analysis of the CYP1B1 gene in Pakistani primary congenital glaucoma patients: Identification of four known and a novel causative variant at the 3′ splice acceptor site of intron 2.
- Published in:
- Congenital Anomalies, 2019, v. 59, n. 5, p. 152, doi. 10.1111/cga.12312
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- Publication type:
- Article
3
Ring chromosome 6 in a child with anterior segment dysgenesis and review of its overlap with other FOXC1 deletion phenotypes.
- Published in:
- Congenital Anomalies, 2019, v. 59, n. 5, p. 174, doi. 10.1111/cga.12309
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- Publication type:
- Article
4
Natural histories of patients with Wolf‐Hirschhorn syndrome derived from variable chromosomal abnormalities.
- Published in:
- Congenital Anomalies, 2019, v. 59, n. 5, p. 169, doi. 10.1111/cga.12318
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- Publication type:
- Article
5
Clinical study of dentocraniofacial characteristics in patients with Williams syndrome.
- Published in:
- Congenital Anomalies, 2019, v. 59, n. 5, p. 162, doi. 10.1111/cga.12316
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- Publication type:
- Article
6
Novel insertion and a previously reported nonsense variant of ALOXE3 gene lead to autosomal recessive ichthyosis in two Balochi families.
- Published in:
- Congenital Anomalies, 2019, v. 59, n. 5, p. 179, doi. 10.1111/cga.12311
- By:
- Publication type:
- Article
7
Issue Information.
- Published in:
- Congenital Anomalies, 2019, v. 59, n. 5, p. 149, doi. 10.1111/cga.12299
- Publication type:
- Article