Works matching IS 09646906 AND DT 1997 AND VI 6 AND IP 4
Results: 20
Co-Ordinate Regulation of the Cystic Fibrosis and Multidrug Resistance Genes in Cystic Fibrosis Knockout Mice.
- Published in:
- Human Molecular Genetics, 1997, v. 6, n. 4, p. 527, doi. 10.1093/hmg/6.4.527
- By:
- Publication type:
- Article
Murine Mucopolysaccharidosis Type I: Targeted Disruption of the Murine α-l-Iduronidase Gene.
- Published in:
- Human Molecular Genetics, 1997, v. 6, n. 4, p. 503, doi. 10.1093/hmg/6.4.503
- By:
- Publication type:
- Article
Identification of a Self-Association Region Within the SCA1 Gene Product, Ataxin-1.
- Published in:
- Human Molecular Genetics, 1997, v. 6, n. 4, p. 513, doi. 10.1093/hmg/6.4.513
- By:
- Publication type:
- Article
A Functional Polymorphism in the Promoter Region of the Dopamine D2 Receptor Gene Is Associated with Schizophrenia.
- Published in:
- Human Molecular Genetics, 1997, v. 6, n. 4, p. 577, doi. 10.1093/hmg/6.4.577
- By:
- Publication type:
- Article
A Duplication of 12 bp in the Critical Cysteine Rich Domain of the RET Proto-Oncogene Results in a Distinct Phenotype of Multiple Endocrine Neoplasia Type 2A.
- Published in:
- Human Molecular Genetics, 1997, v. 6, n. 4, p. 587, doi. 10.1093/hmg/6.4.587
- By:
- Publication type:
- Article
Localisation of a Gene for Dominant Cone-Rod Dystrophy (CORD6) to Chromosome 17p.
- Published in:
- Human Molecular Genetics, 1997, v. 6, n. 4, p. 597, doi. 10.1093/hmg/6.4.597
- By:
- Publication type:
- Article
Identification of the Syrian Hamster Cardiomyopathy Gene.
- Published in:
- Human Molecular Genetics, 1997, v. 6, n. 4, p. 601, doi. 10.1093/hmg/6.4.601
- By:
- Publication type:
- Article
Distribution of Mutations in the PEX Gene in Families with X-linked Hypophosphataemic Rickets (HYP).
- Published in:
- Human Molecular Genetics, 1997, v. 6, n. 4, p. 539, doi. 10.1093/hmg/6.4.539
- By:
- Publication type:
- Article
Identification of the Gene Encoding the Human Mitochondrial RNA Polymerase (h-mtRPOL) by Cyberscreening of the Expressed Sequence Tags Database.
- Published in:
- Human Molecular Genetics, 1997, v. 6, n. 4, p. 615, doi. 10.1093/hmg/6.4.615
- By:
- Publication type:
- Article
Analysis of the Steroidogenic Acute Regulatory Protein (StAR) Gene in Japanese Patients with Congenital Lipoid Adrenal Hyperplasia.
- Published in:
- Human Molecular Genetics, 1997, v. 6, n. 4, p. 571, doi. 10.1093/hmg/6.4.571
- By:
- Publication type:
- Article
Tumour Necrosis Factor Haplotypes and Asthma.
- Published in:
- Human Molecular Genetics, 1997, v. 6, n. 4, p. 551, doi. 10.1093/hmg/6.4.551
- By:
- Publication type:
- Article
Iraqi-Jewish Kindreds with Optic Atrophy Plus (3-Methylglutaconic Aciduria Type 3) Demonstrate Linkage Disequilibrium with the CTG Repeat in the 3′ Untranslated Region of the Myotonic Dystrophy Protein Kinase Gene.
- Published in:
- Human Molecular Genetics, 1997, v. 6, n. 4, p. 563, doi. 10.1093/hmg/6.4.563
- By:
- Publication type:
- Article
Linkage and Physical Mapping of X-Linked Lissencephaly/SBH (XLIS): A Gene Causing Neuronal Migration Defects in Human Brain.
- Published in:
- Human Molecular Genetics, 1997, v. 6, n. 4, p. 555, doi. 10.1093/hmg/6.4.555
- By:
- Publication type:
- Article
Loci for Classical and a Variant Late Infantile Neuronal Ceroid Lipofuscinosis Map to Chromosomes 11p15 and 15q21–23.
- Published in:
- Human Molecular Genetics, 1997, v. 6, n. 4, p. 591, doi. 10.1093/hmg/6.4.591
- By:
- Publication type:
- Article
Inhibition of Fibrillin 1 Expression Using U1 snRNA as a Vehicle for the Presentation of Antisense Targeting Sequence.
- Published in:
- Human Molecular Genetics, 1997, v. 6, n. 4, p. 519, doi. 10.1093/hmg/6.4.519
- By:
- Publication type:
- Article
Identification of Nine Novel Mutations in the Hepatocyte Nuclear Factor 1 Alpha Aene Associated with Maturity-Onset Diabetes of the Young (MODY3).
- Published in:
- Human Molecular Genetics, 1997, v. 6, n. 4, p. 583, doi. 10.1093/hmg/6.4.583
- By:
- Publication type:
- Article
Double-Strand Breaks May Initiate the Inversion Mutation Causing the Hunter Syndrome.
- Published in:
- Human Molecular Genetics, 1997, v. 6, n. 4, p. 627, doi. 10.1093/hmg/6.4.627
- By:
- Publication type:
- Article
Location of the First Genetic Locus, PKDr1, Controlling Autosomal Dominant Polycystic Kidney Disease in Han:SPRD cy/+ rat.
- Published in:
- Human Molecular Genetics, 1997, v. 6, n. 4, p. 609, doi. 10.1093/hmg/6.4.609
- By:
- Publication type:
- Article
Mapping of the Familial Infantile Myasthenia (Congenital Myasthenic Syndrome Type Ia) Gene to Chromosome 17p with Evidence of Genetic Homogeneity.
- Published in:
- Human Molecular Genetics, 1997, v. 6, n. 4, p. 635, doi. 10.1093/hmg/6.4.635
- By:
- Publication type:
- Article
Identification of Three Different Truncating Mutations in Cytochrome P4501B1 (CYP1B1) as the Principal Cause of Primary Congenital Glaucoma (Buphthalmos) in Families Linked to the GLC3A Locus on Chromosome 2p21.
- Published in:
- Human Molecular Genetics, 1997, v. 6, n. 4, p. 641, doi. 10.1093/hmg/6.4.641
- By:
- Publication type:
- Article