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Dai-Dyi Town Selected Research

Duplication 15q11-q13 Syndrome

10/2018Prenatal diagnosis of a familial 15q11.2 (BP1-BP2) microdeletion encompassing TUBGCP5, CYFIP1, NIPA2 and NIPA1 in a fetus with ventriculomegaly, microcephaly and intrauterine growth restriction on prenatal ultrasound.

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Dai-Dyi Town Research Topics

Disease

7Uniparental Disomy
07/2021 - 12/2012
4Down Syndrome (Down's Syndrome)
05/2021 - 09/2020
2Trisomy (Trisomies)
11/2020 - 12/2010
2Trisomy 18 Syndrome
07/2020 - 06/2011
1Chromosome Aberrations (Chromosome Abnormalities)
05/2021
1Esophageal Atresia
03/2021
1Persistent Left Superior Vena Cava
03/2021
1Fetal Distress
03/2021
1Polyhydramnios
03/2021
1Spontaneous Abortion (Miscarriage)
09/2020
1Triploidy
12/2018
1Duplication 15q11-q13 Syndrome
10/2018
1tetrasomy 18p Chromosome 18
12/2012
1Fetal Death
09/2012
1Chromosome Deletion (Deletion, Chromosome)
12/2010

Drug/Important Bio-Agent (IBA)

11Genetic Markers (Genetic Marker)IBA
07/2021 - 09/2012
4DNA (Deoxyribonucleic Acid)IBA
01/2021 - 12/2010
1dimemorfan (AT 17)IBA
05/2021
1Pregnancy-Associated Plasma Protein-A (PAPP-A)IBA
09/2020
1Estriol (Epiestriol)IBA
06/2011
1Fetal Proteins (Fetoprotein)IBA
06/2011
1Chorionic Gonadotropin (Human Chorionic Gonadotropin)FDA LinkGeneric
06/2011
1inhibin AIBA
06/2011

Therapy/Procedure

1Cesarean Section (Caesarean Section)
03/2021
1Gastric Balloon
03/2021