スポンサーリンク
Department of Human Genetics Nagasaki University School of Medicine | 論文
- The gene for mesomelic dysplasia Kantaputra type is mapped to chromosome 2q24-q32
- Immunocytochemical study of activin type IB receptor (XALK4) in Xenopus oocytes
- Hyperlipemia and Early Pancreatic Injury Induced by Ethanol Intake in Rats
- PHYSICAL MAP OF A YAC CONTIG CONTAINING THE REGION OF THE HUMAN GENE (HYRC) COMPLEMENTING HYPER-RADIOSENSITIVITY OF THE SCID MOUSE MUTATION
- Repeat-directed isolation of a novel gene preferentially expressed from the maternal allele in human placenta
- A SacII polymorphism in the human ASCL2 (HASH2) gene region
- A case of Schinzel-Giedion syndrome complicated with progressive severe gingival hyperplasia and progressive brain atrophy
- A case of megalocornea-mental retardation syndrome complicated with bilateral sensorineural hearing impairment
- Autosomal dominant onychodystrophy and congenital sensorineural deafness
- A severe case of Moebius syndrome with calcification on the fourth ventricular floor
- New radiological finding by magnetic resonance imaging examination of the brain in Coffin-Lowry syndrome
- A NAGER ACROFACIAL DYSOSTOSIS SYNDROME PATIENT WITH SEVERE RESPIRATORY DISTRESS SYNDROME (RDS)
- The Energetic Particle Spectrometer HEP onboard the GEOTAIL Spacecraft
- Painting of Chinese hamster chromosomes with chromosome specific probes constructed by microdissection and sorting
- A Novel Imprinted Gene, KCNQ1DN, within the WT2 Critical Region of Human Chromosome 11p15.5 and Its Reduced Expression in Wilm's Tumors^1
- A case of achondroplasia with severe respiratory failure, profound developmental delay and hypercreatine phosphokinasemia
- Mechanisms for the Occurrence of Three Uniparental Disomies Associated with Abnormal Phenotypes
- A Hhal/BstUl polymorphism in a novel gene at human chromosome 11p15.5
- Search for active endogenous retroviruses: identification and characterization of a HERV-E gene that is expressed in the pancreas and thyroid
- Maternal Uniparental Disomy for Chromosome 14 with Diabetes Mellitus