Works matching IS 00015652 AND DT 1995 AND VI 45 AND IP 2

Results: 10

Parallel Computation of Genetic Likelihoods Using CRI-MAP, PVM, and a Network of Distributed Workstations.

Published in:

Human Heredity, 1995, v. 45, n. 2, p. 103, doi. 10.1159/000154268

By:

Matise, Tara Cox;
Schroeder, Mark D.;
Chiarulli, Donald M.;
Weeks, Daniel E.

Publication type:

Article

Orosomucoid Types in Allergic Contact Dermatitis.

Published in:

Human Heredity, 1995, v. 45, n. 2, p. 117, doi. 10.1159/000154269

By:

Fan, Chaohong

Publication type:

Article

DNA Polymorphisms and Haplotypes of Human Liver/Bone/Kidney Alkaline Phosphatase in Finns, Saamis and Swedes.

Published in:

Human Heredity, 1995, v. 45, n. 2, p. 61, doi. 10.1159/000154260

By:

Wennberg, C.;
Sikström, C.

Publication type:

Article

Down's Syndrome in Saudi Arabia: Incidence and Cytogenetics.

Published in:

Human Heredity, 1995, v. 45, n. 2, p. 65, doi. 10.1159/000154261

By:

Niazi, Meena A.;
Al-Mazyad, Abdullah S.;
Al-Husain, Muneera A.;
Al-Mofada, Saleh M.;
Al-Zamil, Fahad A.;
Khashoggi, Tariq Y.;
Al-Eissa, Youssef A.

Publication type:

Article

Study of the 3'-ApoB Minisatellite Performed by PCR in the Population of Catalonia (Northeast Spain).

Published in:

Human Heredity, 1995, v. 45, n. 2, p. 70, doi. 10.1159/000154262

By:

Gené, M.;
Huguet, E.;
Sánchez-García, C.;
Moreno, P.;
Corbella, J.;
Mezquita, J.

Publication type:

Article

Refined Localization of Human Peroxisomal 3-Oxoacyl-CoA Thiolase (ACAA) to 3p22.

Published in:

Human Heredity, 1995, v. 45, n. 2, p. 75, doi. 10.1159/000154263

By:

Ottone, F.;
Raimondi, E.;
Rocchi, M.;
Giussani, F.;
Malcovati, M.;
Tenchini, M.L.

Publication type:

Article

Neutral Polymorphisms in the Deletion-Prone Regions of the Dystrophin Gene.

Published in:

Human Heredity, 1995, v. 45, n. 2, p. 80, doi. 10.1159/000154264

By:

Ziętkiewicz, Ewa;
Akalin, Nur;
Labuda, Damian

Publication type:

Article

Ethnic Differences in Allele Frequencies of Two Microsatellite Markers Closely Linked to the Locus for Polycystic Kidney Disease 1 (PKD1).

Published in:

Human Heredity, 1995, v. 45, n. 2, p. 84, doi. 10.1159/000154265

By:

Wang, Huiru;
Kuwata, Shoji;
Juji, Takeo;
Yanagisawa, Masami;
Tokunaga, Katsushi;
Horie, Shigeo;
Higashihara, Eiji;
Kurokawa, Kiyoshi;
Yoshikura, Hiroshi;
Shibata, Yoichi

Publication type:

Article

Chromosome 6p Microsatellite Polymorphisms in African-Americans.

Published in:

Human Heredity, 1995, v. 45, n. 2, p. 90, doi. 10.1159/000154266

By:

Maliarik, Mary J.;
Kost, James A.;
Harrington, Douglas W.;
Popovich, Jr., John;
Major, Marcie L.;
Rybicki, Benjamin A.;
Iannuzzi, Michael C.

Publication type:

Article

Characterisation of Nucleotide Sequence Variants and Disease-Specific Mutations Involving the 3' End of the C1-Inhibitor Gene in Hereditary Angio-Oedema.

Published in:

Human Heredity, 1995, v. 45, n. 2, p. 98, doi. 10.1159/000154267

By:

Siddique, Z.;
McPhaden, A.R.;
Whaley, K.

Publication type:

Article