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Wayseen Wang Selected Research

dimemorfan (AT 17)

7/2022High-level mosaicism for 45,X in 45,X/46,XX at amniocentesis in a pregnancy with a favorable outcome and postnatal progressive decrease of the 45,X cell line.
3/2022Detection of paternal origin of fetal de novo rea(21q;21q) down syndrome in a pregnancy of a young woman associated with an abnormal first-trimester maternal serum screening result.
3/2022Prenatal diagnosis and molecular cytogenetic characterization of mosaic ring chromosome 21 associated with low PAPP-A and low PlGF in the first-trimester maternal serum screening.
7/2021Prenatal diagnosis of recurrent mosaic ring chromosome 13 of maternal origin.
5/2021Prenatal diagnosis of mosaicism for double aneuploidy of 47,XXY and trisomy 7 (48,XXY,+7) at amniocentesis in a pregnancy with a favorable outcome.
11/2019Detection of a familial 1q21.1 microdeletion and concomitant CHD1L mutation in a fetus with oligohydramnios and bilateral renal dysplasia on prenatal ultrasound.
9/2019Detection of de novo del(18)(q22.2) and a familial of 15q13.2-q13.3 microduplication in a fetus with congenital heart defects.
2/2018Prenatal diagnosis of a 0.7-Mb 17p13.3 microdeletion encompassing YWHAE and CRK but not PAFAH1B1 in a fetus without ultrasound abnormalities.
8/2017Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 16.
2/2017Familial transmission of recurrent 15q11.2 (BP1-BP2) microdeletion encompassing NIPA1, NIPA2, CYFIP1, and TUBGCP5 associated with phenotypic variability in developmental, speech, and motor delay.
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Wayseen Wang Research Topics

Disease

30Uniparental Disomy
07/2022 - 09/2010
17Down Syndrome (Down's Syndrome)
07/2022 - 05/2003
8Trisomy (Trisomies)
07/2022 - 12/2010
6Trisomy 18 Syndrome
07/2022 - 03/2011
6Fetal Growth Retardation (Intrauterine Growth Retardation)
01/2022 - 06/2010
4Ring Chromosomes (Ring Chromosome)
03/2022 - 06/2011
4Trisomy 13 Syndrome
01/2022 - 03/2011
4Oligohydramnios
09/2020 - 12/2013
3Aneuploidy (Aneuploid)
07/2021 - 03/2011
3Polyhydramnios
03/2021 - 12/2010
3Rhabdomyoma
09/2013 - 02/2005
3Osteogenesis Imperfecta (Lobstein Disease)
06/2012 - 02/2006
2Pre-Eclampsia (Preeclampsia)
03/2022 - 01/2022
2Chromosome Aberrations (Chromosome Abnormalities)
05/2021 - 01/2020
2Fetal Distress
03/2021 - 02/2005
2Spontaneous Abortion (Miscarriage)
09/2020 - 06/2017
2Ventricular Heart Septal Defects (Ventricular Septal Defect)
09/2019 - 06/2016
2Isochromosomes
12/2017 - 02/2015
2Microcephaly
02/2014 - 09/2013
2Cysts
12/2013 - 06/2013
2Congenital Abnormalities (Deformity)
09/2013 - 01/2006
2Tuberous Sclerosis (Bourneville's Disease)
09/2013 - 07/2006
2Hypertelorism
06/2013 - 06/2003
2Chromosome Deletion (Deletion, Chromosome)
06/2011 - 12/2010
2Holoprosencephaly (Arhinencephaly)
03/2011 - 09/2003
2Ascites
06/2010 - 09/2007
1Esophageal Atresia
03/2021
1Persistent Left Superior Vena Cava
03/2021
115q24 Microdeletion
05/2020
1Pericardial Effusion
09/2019
1Cardiomegaly (Heart Hypertrophy)
09/2019
1Triploidy
12/2018
1Duplication 15q11-q13 Syndrome
10/2018
1Spinocerebellar Ataxias (Spinocerebellar Ataxia)
02/2018
1Obesity
12/2016
1Intellectual Disability (Idiocy)
12/2016
1Attention Deficit Disorder with Hyperactivity (Attention Deficit Hyperactivity Disorder)
12/2016
1Language Development Disorders (Semantic-Pragmatic Disorder)
06/2016
1DiGeorge Syndrome (Syndrome, DiGeorge)
02/2016
1Craniosynostoses (Craniosynostosis)
02/2014
1Scimitar Syndrome
09/2013
1Schmid-Fraccaro syndrome
09/2013
1Epilepsy (Aura)
09/2013
1Acrocephalosyndactylia (Apert Syndrome)
06/2013
1Syndactyly (Polysyndactyly)
06/2013
1Type IV Osteogenesis Imperfecta
03/2013
1Type 2 Diabetes Mellitus (MODY)
12/2012
1tetrasomy 18p Chromosome 18
12/2012
1Pyelectasis
09/2012
1Fetal Death
09/2012
1Cystic Lymphangioma (Hygroma)
03/2011
1Umbilical Hernia (Omphalocele)
03/2011
1Hydronephrosis
03/2011
1Microvillus inclusion disease
12/2010
1Congenital chloride diarrhea
12/2010
1Diarrhea
12/2010
1Echogenic Bowel
06/2010
1Cytomegalovirus Infections (Inclusion Disease)
06/2010
1Klippel-Trenaunay-Weber Syndrome (Syndrome, Klippel-Trenaunay-Weber)
09/2007
1Glycogen Storage Disease Type II (Pompe's Disease)
03/2004
1Congenital Diaphragmatic Hernias
01/2004
1Micrognathism
06/2003
1Premature Obstetric Labor (Premature Labor)
05/2003
1Type I Thanatophoric Dysplasia
08/2002
1Hemorrhage
03/2002
1Placenta Accreta
03/2002
1Uterine Inertia
03/2002

Drug/Important Bio-Agent (IBA)

49Genetic Markers (Genetic Marker)IBA
07/2022 - 09/2003
16dimemorfan (AT 17)IBA
07/2022 - 01/2006
13DNA (Deoxyribonucleic Acid)IBA
07/2022 - 06/2010
6Pregnancy-Associated Plasma Protein-A (PAPP-A)IBA
03/2022 - 02/2014
5dichlorobis(azomycin)platinum IIIBA
07/2022 - 10/2017
5alpha-Fetoproteins (alpha-Fetoprotein)IBA
09/2007 - 05/2003
3trans-sodium crocetinate (crocetin)IBA
09/2013 - 02/2005
3Fetal Proteins (Fetoprotein)IBA
03/2013 - 06/2011
3Estriol (Epiestriol)IBA
03/2013 - 06/2011
3Chorionic Gonadotropin (Human Chorionic Gonadotropin)FDA LinkGeneric
03/2013 - 06/2011
3alpha2 Subunit Collagen Type IIBA
03/2013 - 02/2006
3inhibin AIBA
03/2013 - 06/2011
2Intercellular Signaling Peptides and Proteins (Growth Factors)IBA
03/2022 - 11/2021
2OligonucleotidesIBA
12/2017 - 09/2012
1Cytochrome P-450 CYP1A1 (CYP1A1)IBA
05/2020
1Cholesterol Side-Chain Cleavage Enzyme (CYP11A1)IBA
05/2020
1Cytochrome P-450 CYP1A2 (CYP1A2)IBA
05/2020
1Anticonvulsants (Antiepileptic Drugs)IBA
09/2013
1Diphosphonates (Bisphosphonates)IBA
06/2012
1SodiumIBA
12/2010
1Nonsense Codon (Nonsense Mutation)IBA
07/2006
1AcidsIBA
03/2004
1alpha-Glucosidases (Acid Maltase)IBA
03/2004
1GlycogenIBA
03/2004
1Codon (Codons)IBA
08/2002

Therapy/Procedure

5Cesarean Section (Caesarean Section)
03/2021 - 03/2002
4Ligation
07/2022 - 03/2011
1Gastric Balloon
03/2021
1Colonic Pouches (S Pouch)
06/2013
1Glycemic Control
12/2012
1Therapeutics
12/2012
1Sutures (Suture)
06/2003