Fetal Gonadal Development : An Overview
スポンサーリンク
概要
- 論文の詳細を見る
- 2001-12-01
著者
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Ogata Tsutomu
Department Of Endocrinology And Metabolism National Research Institute For Child Health And Developm
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Ogata Tsutomu
Department Of Pediatrics Tokyo Electric Power Company Hospital
関連論文
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- Identification of novel RMRP mutations and specific founder haplotypes in Japanese patients with cartilage-hair hypoplasia
- Determination of specific activities and kinetic constants of biotinidase and lipoamidase in LEW rat and Lactobacillus casei (Shirota)
- Identification and characterization of cryptic SHOX intragenic deletions in three Japanese patients with Leri-Weill dyschondrosteosis
- Statural Growth in 31 Japanese Patients with SHOX Haploinsufficiency : Support for a Disadvantageous Effect of Gonadal Estrogens
- Kallmann Syndrome Phenotype in a Female Patient with CHARGE Syndrome and CHD7 Mutation
- Association of Micropenis with Pro185Ala Polymorphism of the Gene for Aryl Hydrocarbon Receptor Repressor Involved in Dioxin Signaling
- A Case of XYY Syndrome with Short Stature
- Mental Retardation in A Girl with Turner's Syndrome with An Active Ring X Chromosome Missing XIST
- Incidental deviation of short and long CAG repeats in the androgen receptor gene for Japanese male infertility
- Growth Hormone and Gonadotropin-Releasing Hormone Analog Therapy in Haploinsufficiency of SHOX
- KRAS Analysis in 34 Noonan Syndrome Patients without PTPN11 Mutation
- Fetal Gonadal Development : An Overview
- Association of Common LH Variant with Hyperfunctional Promoter in a Japanese Infertile Woman
- Target Height and Target Range for Japanese Children : Revisited
- Clinical findings and P450 Oxidoreductase (POR) gene analysis in Antley-Bixler syndrome with abnormal genitalia
- Imaging of congenital lipoid adrenal hyperplasia
- Determination of biotin (vitamin H) by the high-performance affinity chromatography with a trypsin-treated avidin-bound column
- Mental Retardation in a Boy with Congenital Adrenal Hypoplasia : A Clue to Contiguous Gene Syndrome Involving DAX1 and IL1RAPL
- Lymphstasis in a Boy with Noonan Syndrome : Imprication for the Development of Skeletal Features
- Haploinsufficiency of SHOX : Clinical Variability and Its Underlying Cause
- Genetics of Human Growth
- GATA3 abnormalities in six patients with HDR syndrome
- Diabetes Mellitus in a Japanese Girl with HDR Syndrome and GATA3 Mutation
- Identification of chromosome 15q26 terminal deletion with telomere sequences and its bearing on genotype-phenotype analysis
- Androgenetic/biparental mosaicism in a girl with Beckwith-Wiedemann syndrome-like and upd(14)pat-like phenotypes
- Maternal age effect on the development of Prader-Willi syndrome resulting from upd(15)mat through meiosis 1 errors
- Haplotype analysis of ESR2 in Japanese patients with spermatogenic failure
- Association of variants in genes involved in environmental chemical metabolism and risk of cryptorchidism and hypospadias
- Skeletal Deformity Associated with SHOX Deficiency
- Submicroscopic deletion involving fibroblast growth factor receptor 1 gene in a patient with combined pituitary hormone deficiency
- A novel homozygous mutation of the nicotinamide nucleotide transhydrogenase gene in a Japanese patient with familial glucocorticoid deficiency