about
Molecular analysis of the Y chromosome AZFc region in Japanese infertile males with spermatogenic defects.A Case of Thanatophoric Dysplasia Type I with Fetal Hydrops in the First Trimester.A large seminoma occurring 20 years after diagnosis of complete androgen insensitivity syndrome: A case reportSurvey of prenatal testing for genetic disorders in Japan: Recent report.Current status of non-invasive prenatal testing in Japan.Follow-Up Study on Fetal CT Radiation Dose in Japan: Validating the Decrease in Radiation Dose.Nationwide survey for current clinical status of amniocentesis and maternal serum marker test in Japan.Fetal cell-free DNA fraction in maternal plasma is affected by fetal trisomy.Bone morphogenetic protein-2 counterregulates interleukin-18 mRNA and protein in MC3T3-E1 mouse osteoblastic cells.Direct production of the Fab fragment derived from the sperm immobilizing antibody using polymerase chain reaction and cDNA expression vectors.Stable production of recombinant human sperm immobilizing antibody using cDNA expression vectors.Chromosome abnormalities diagnosed in utero: a Japanese study of 28 983 amniotic fluid specimens collected before 22 weeks gestations.Development of an integrated support system for hereditary cancer and its impact on gynecologic services.Nationwide radiation dose survey of computed tomography for fetal skeletal dysplasias.Cloning and expression of the rat class I MHC gene RT1.Al.Parental serum alkaline phosphatase activity as an auxiliary tool for prenatal diagnosis of hypophosphatasia.Pig zona pellucida 2 (pZP2) protein does not participate in zona pellucida formation in transgenic mice.The current state of genetic counseling before and after amniocentesis for fetal karyotyping in Japan: a survey of obstetric hospital clients of a prenatal testing laboratory.Possible presence of O-linked carbohydrate in the human male reproductive tract CD52.Severe perinatal hypophosphatasia due to homozygous deletion of T at nucleotide 1559 in the tissue nonspecific alkaline phosphatase gene.Epitope analysis for human sperm-immobilizing monoclonal antibodies, MAb H6-3C4, 1G12 and campath-1.Fetal cell-free DNA fraction in maternal plasma for the prediction of hypertensive disorders of pregnancy.Statin treatment rescues FGFR3 skeletal dysplasia phenotypes.Modeling type II collagenopathy skeletal dysplasia by directed conversion and induced pluripotent stem cells.Criteria for radiologic diagnosis of hypochondroplasia in neonates.A novel mutation Ser344Cys in FGFR3 causes achondroplasia with severe platyspondyly.Factors affecting parental decisions to terminate pregnancy in the presence of chromosome abnormalities: a Japanese multicenter study.Studies on the RT1.E locus of the rat major histocompatibility complexPrenatal diagnosis of achondroplasia using the nested polymerase chain reaction with modified primer setsMolecular analysis of familial androgen insensitivity syndrome due to replacement of glutamic acid 802 by lysinePrenatal diagnosis of thanatophoric dysplasia by mutational analysis of the fibroblast growth factor receptor 3 gene and a proposed correction of previously published PCR resultsRadiographic and genetic diagnosis of sporadic hypochondroplasia early in the neonatal periodNovel missense mutation resulting in the substitution of tyrosine by cysteine at codon 597 of the type X collagen gene associated with Schmid metaphyseal chondrodysplasiaPrenatal sonographic diagnosis of a fetal renal mesoblastic nephroma occurring after transfer of a cryopreserved embryoPrenatal diagnosis of short-rib polydactyly syndrome type 3 (Verma-Naumoff type) by three-dimensional helical computed tomographyPrevalence of c.1559delT in ALPL, a common mutation resulting in the perinatal (lethal) form of hypophosphatasia in Japanese and effects of the mutation on heterozygous carriersA compound heterozygote harboring novel and recurrent DTDST mutations with intermediate phenotype between atelosteogenesis type II and diastrophic dysplasiaPrenatal diagnosis of Kniest dysplasia with three-dimensional helical computed tomographyPlatyspondylic lethal skeletal dysplasia San Diego type (thanatophoric dysplasia type 1) associated with trisomy 21 presenting with nuchal translucency: a case reportThe current status of umbilical cord blood collection in Japanese medical centers: survey of obstetricians
P50
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P50
description
researcher
@en
name
H Sawai
@en
H Sawai
@nl
type
label
H Sawai
@en
H Sawai
@nl
prefLabel
H Sawai
@en
H Sawai
@nl
P106
P31
P496
0000-0002-8997-464X