Glucose-6-Phosphate Dehydrogenase Deficiency in Kuwait, Syria, Egypt, Iran, Jordan and Lebanon.
- Published in:
- Human Heredity, 2000, v. 50, n. 3, p. 158, doi. 10.1159/000022906
- By:
- Publication type:
- Article
Works matching IS 00015652 AND DT 2000 AND VI 50 AND IP 3
Results: 13
1
2
Screening of Deletions in SMN, NAIP and BTF2p44 Genes in Turkish Spinal Muscular Atrophy Patients.
- Published in:
- Human Heredity, 2000, v. 50, n. 3, p. 162, doi. 10.1159/000022907
- By:
- Publication type:
- Article
3
Linkage of Hereditary Distal Myopathy with Desmin Accumulation to 2q.
- Published in:
- Human Heredity, 2000, v. 50, n. 3, p. 166, doi. 10.1159/000022908
- By:
- Publication type:
- Article
4
Analysis of the SMN and NAIP Genes in Slovak Spinal Muscular Atrophy Patients.
- Published in:
- Human Heredity, 2000, v. 50, n. 3, p. 171, doi. 10.1159/000022909
- By:
- Publication type:
- Article
5
Allelic Frequencies of FBN1 Gene Polymorphisms and Genetic Analysis of Italian Families with Marfan Syndrome.
- Published in:
- Human Heredity, 2000, v. 50, n. 3, p. 175, doi. 10.1159/000022910
- By:
- Publication type:
- Article
6
Search for Coeliac Disease Susceptibility Loci on 7q11.23 Candidate Region: Absence of Association with the ELN17 Microsatellite Marker.
- Published in:
- Human Heredity, 2000, v. 50, n. 3, p. 180, doi. 10.1159/000022911
- By:
- Publication type:
- Article
7
Testing Mode of Inheritance of a Candidate Mutation at a Quantitative Trait Locus.
- Published in:
- Human Heredity, 2000, v. 50, n. 3, p. 184, doi. 10.1159/000022912
- By:
- Publication type:
- Article
8
Allelic Affinities between the F13A Common Gene Products Inferred by the Analysis of an (AAAG)n STR Polymorphism within the 5′ Untranslated Region.
- Published in:
- Human Heredity, 2000, v. 50, n. 3, p. 189, doi. 10.1159/000022913
- By:
- Publication type:
- Article
9
A Note on a Conditional-Likelihood Approach for Family-Based Association Studies of Candidate Genes.
- Published in:
- Human Heredity, 2000, v. 50, n. 3, p. 194, doi. 10.1159/000022914
- By:
- Publication type:
- Article
10
Prenatal Determination of a Variable Number of Tandem Repeats in Intron 40 of the von Willebrand Factor Gene from Maternal Peripheral Blood Using the Polymerase Chain Reaction.
- Published in:
- Human Heredity, 2000, v. 50, n. 3, p. 201, doi. 10.1159/000022915
- By:
- Publication type:
- Article
11
Linkage Analysis for Diseases with Variable Age of Onset.
- Published in:
- Human Heredity, 2000, v. 50, n. 3, p. 205, doi. 10.1159/000022916
- By:
- Publication type:
- Article
12
Announcement.
- Published in:
- Human Heredity, 2000, v. 50, n. 3, p. 210, doi. 10.1159/000022917
- Publication type:
- Article
13
Physical and cDNA Mapping in the DBH Region of Human Chromosome 9q34.
- Published in:
- Human Heredity, 2000, v. 50, n. 3, p. 151, doi. 10.1159/000022905
- By:
- Publication type:
- Article