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  Human Heredity: Volume 50, No. 3, 2000  
  February 23, 2000

virtual library in human genetics and molecular biology

 
     
J. Ott, New York, N.Y.
S. Karger AG
  Date of publishing: February, 2000  
 



Original Papers
Physical and cDNA Mapping in the DBH Region of Human Chromosome 9q34
Gilbert, J.R. (Durham, N.C.); Kumar, A. (Cleveland, Ohio); Newey, S. (Oxford); Rao, N. (Winston-Salem, N.C.); Ioannou, P. (Nicosia); Qiu, H.; Lin, D.; Xu, P. (Durham, N.C.); Pettenati, M.J. (Winston-Salem, N.C.); Pericak-Vance, M.A. (Durham, N.C.)

Glucose-6-Phosphate Dehydrogenase Deficiency in Kuwait, Syria, Egypt, Iran, Jordan and Lebanon
Usanga, E.A.; Ameen, R. (Kuwait)

Screening of Deletions in SMN, NAIP and BTF2p44 Genes in Turkish Spinal Muscular Atrophy Patients
Savas, S.; Gokgoz, N.; Kayserili, H. (Istanbul); Ozkinay, F. (Izmir); Yuksel-Apak, M.; Kirdar, B. (Istanbul)

Linkage of Hereditary Distal Myopathy with Desmin Accumulation to 2q
Saavedra-Matiz, C.A. (Albany, N.Y.); Chapman, N.H.; Wijsman, E.M. (Seattle, Wash.); Horowitz, S.H. (Columbia, Mo.); Rosen, D.R. (Albany, N.Y.)

Analysis of the SMN and NAIP Genes in Slovak Spinal Muscular Atrophy Patients

Zat’ková, A. (Bratislava); Hahnen, E.; Wirth, B. (Bonn); ´Kádasi, L. (Bratislava)
Allelic Frequencies of FBN1 Gene Polymorphisms and Genetic Analysis of Italian Families with Marfan Syndrome
Mottes, M.; Mirandola, S.; Rigatelli, F.; Zolezzi, F.; Lisi, V. (Verona); Gordon, D. (New York, N.Y.); Pignatti, P.F. (Verona)

Search for Coeliac Disease Susceptibility Loci on 7q11.23 Candidate Region: Absence of Association with the ELN17 Microsatellite Marker
Grillo, R.; Petronzelli, F.; Mora, B.; Bonamico, M.; Mazzilli, M.C. (Rome)

Testing Mode of Inheritance of a Candidate Mutation at a Quantitative Trait Locus
Rabinowitz, D. (New York, N.Y.); Zanchi, A.; Schaumberg, D.; Krolewski, A. (Boston, Mass.)

Allelic Affinities between the F13A Common Gene Products Inferred by the Analysis of an (AAAG)n STR Polymorphism within the 5’ Untranslated Region
Prata, M.J.; Miranda, C.; Rocha, J.; Amorim, A. (Porto)

A Note on a Conditional-Likelihood Approach for Family-Based Association Studies of Candidate Genes
Hsu, L.; Zhao, L.P.; Aragaki, C. (Seattle, Wash.)

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
Ni, X.; Guo, J. (Guangzhou); Xia, J.; Li, L. (Changsha)

Linkage Analysis for Diseases with Variable Age of Onset
Siegmund, K.D. (Los Angeles, Calif.); Todorov, A.A. (St. Louis, Mo.)



 
     
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