about
NOBOX deficiency disrupts early folliculogenesis and oocyte-specific gene expressionNobox is a homeobox-encoding gene preferentially expressed in primordial and growing oocytes.Genotyping analysis for the 46 C/T polymorphism of coagulation factor XII and the involvement of factor XII activity in patients with recurrent pregnancy loss.A Case of Microangiopathic Antiphospholipid-Associated Syndromes during Pregnancy: Review of the LiteraturePaternal uniparental disomy 14 and related disorders: placental gene expression analyses and histological examinations.Candidate genes for premature ovarian failure.Genetic factors as a cause of miscarriage.Current status of non-invasive prenatal testing in Japan.Background of couples undergoing non-invasive prenatal testing in Japan.Fetal cell-free DNA fraction in maternal plasma is affected by fetal trisomy.No association of C677T methylenetetrahydrofolate reductase and an endothelial nitric oxide synthase polymorphism with recurrent pregnancy loss.Establishment of a polymerase chain reaction method for detection of Escherichia coli in amniotic fluid in patients with chorioamnionitis.Two cases of prenatally diagnosed sacrococcygeal teratoma type I with different clinical features.Psychological distress in post-partum women after non-invasive prenatal testing (NIPT) in Japan.Non-specific psychological distress in women undergoing noninvasive prenatal testing because of advanced maternal age.Prenatal molecular diagnosis of a severe type of L1 syndrome (X-linked hydrocephalus).A survey on awareness of genetic counseling for non-invasive prenatal testing: the first year experience in Japan.Prenatal diagnosis of X-linked recessive Lenz microphthalmia syndrome.Role of cathepsin E in decidual macrophage of patients with recurrent miscarriage.Prenatal diagnosis of persistent cloaca.Role of Indoleamine 2,3-Dioxygenase and Tryptophan 2,3-Dioxygenase in Patients with Recurrent Miscarriage.Prenatal diagnosis of osteogenesis imperfecta type II by three-dimensional ultrasound and computed tomography.Clinical and molecular findings in a patient with 46,XX/47,XX,+14 mosaicism caused by postzygotic duplication of a paternally derived chromosome 14.Factors affecting parental decisions to terminate pregnancy in the presence of chromosome abnormalities: a Japanese multicenter study.Atypical achondroplasia due to somatic mosaicism for the common thanatophoric dysplasia mutation R248C.Management of recurrent miscarriageAbnormal embryonic karyotype is the most frequent cause of recurrent miscarriageSYCP3 mutation may not be associated with recurrent miscarriage caused by aneuploidyIncrease in serum concentrations of inhibin in early onset pre-eclampsia with intrauterine growth restriction.[Prenatal diagnosis and screening]Glycogen storage disease type Ia (GSD Ia) during pregnancy: report of a case complicated by fetal growth restriction and preeclampsiaPrenatal findings of paternal uniparental disomy 14: Delineation of further patientClinical significance of serum growth-regulated oncogene alpha (GROalpha) in patients with gynecological cancerLive birth rate according to maternal age and previous number of recurrent miscarriagesThe biological investigation of prostacyclin in preeclamptic women seen reduced endothelial functionPrenatal findings of omphalocele-exstrophy of the bladder-imperforate anus-spinal defects (OEIS) complexParental decisions following prenatal diagnosis of chromosomal abnormalities: implications for genetic counseling practice in JapanClassification of factors involved in nonreportable results of noninvasive prenatal testing (NIPT) and prediction of success rate of second NIPTEffects of long working hours and shift work during pregnancy on obstetric and perinatal outcomes: A large prospective cohort study-Japan Environment and Children's StudyCompound heterozygous RYR1 mutations by whole exome sequencing in a family with three repeated affected fetuses with fetal akinesia
P50
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P50
description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Nobuhiro Suzumori
@ast
Nobuhiro Suzumori
@en
Nobuhiro Suzumori
@es
Nobuhiro Suzumori
@nl
Nobuhiro Suzumori
@sl
type
label
Nobuhiro Suzumori
@ast
Nobuhiro Suzumori
@en
Nobuhiro Suzumori
@es
Nobuhiro Suzumori
@nl
Nobuhiro Suzumori
@sl
prefLabel
Nobuhiro Suzumori
@ast
Nobuhiro Suzumori
@en
Nobuhiro Suzumori
@es
Nobuhiro Suzumori
@nl
Nobuhiro Suzumori
@sl
P106
P31
P496
0000-0001-9003-1289