Works matching IS 09143505 AND DT 2020 AND VI 60 AND IP 1
Results: 7
Issue Information.
- Published in:
- Congenital Anomalies, 2020, v. 60, n. 1, p. 1, doi. 10.1111/cga.12340
- Publication type:
- Article
Screening of the FANCA gene mutational hotspots in the Pakistani fanconi anemia patients revealed 19 sequence variations.
- Published in:
- Congenital Anomalies, 2020, v. 60, n. 1, p. 32, doi. 10.1111/cga.12331
- By:
- Publication type:
- Article
Intellectual disability and dysmorphic features in male siblings arising from a novel TAF1 mutation.
- Published in:
- Congenital Anomalies, 2020, v. 60, n. 1, p. 40, doi. 10.1111/cga.12330
- By:
- Publication type:
- Article
Association between hereditary predisposition to common cancers and congenital multimalformations.
- Published in:
- Congenital Anomalies, 2020, v. 60, n. 1, p. 22, doi. 10.1111/cga.12329
- By:
- Publication type:
- Article
Bmp4 is an essential growth factor for the initiation of genital tubercle (GT) outgrowth.
- Published in:
- Congenital Anomalies, 2020, v. 60, n. 1, p. 15, doi. 10.1111/cga.12326
- By:
- Publication type:
- Article
Establishment of a simple and rapid method to detect MECP2 duplications using digital polymerase chain reaction.
- Published in:
- Congenital Anomalies, 2020, v. 60, n. 1, p. 10, doi. 10.1111/cga.12325
- By:
- Publication type:
- Article
Antenatal hydronephrosis and fetal urine sampling.
- Published in:
- Congenital Anomalies, 2020, v. 60, n. 1, p. 4, doi. 10.1111/cga.12324
- By:
- Publication type:
- Article