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Results: 1-25/316
Authors:
XIONG MM
GUO SW
Citation: Mm. Xiong et Sw. Guo, THE POWER OF LINKAGE DETECTION BY THE TRANSMISSION DISEQUILIBRIUM TESTS/, Human heredity, 48(6), 1998, pp. 295-312
Authors:
KIM HS
KAMBOH MI
Citation: Hs. Kim et Mi. Kamboh, GENETIC POLYMORPHISMS OF APOLIPOPROTEIN-A-IV, APOLIPOPROTEIN-E AND APOLIPOPROTEIN-H IN KOREANS, Human heredity, 48(6), 1998, pp. 313-317
Authors:
POLTL R
LUCKENBACH C
HIXSON J
RITTER H
Citation: R. Poltl et al., THE SHORT TANDEM REPEAT LOCI HTPO, THO1 AND FGA, Human heredity, 48(6), 1998, pp. 318-324
Authors:
MENOLD MM
SADEH M
LENNON F
BLATT I
GOLDHAMMER Y
YAMAOKA LH
VANCE JM
PERICAKVANCE MA
Citation: Mm. Menold et al., EVIDENCE FOR GENETIC-HETEROGENEITY SUPPORTS CLINICAL DIFFERENCES IN CONGENITAL MYASTHENIC SYNDROMES, Human heredity, 48(6), 1998, pp. 325-332
Authors:
LONJOU C
COLLINS A
BECKMANN J
ALLAMAND V
MORTON N
Citation: C. Lonjou et al., LIMB-GIRDLE MUSCULAR-DYSTROPHY TYPE 2A (CAPN3) - MAPPING USING ALLELIC ASSOCIATION, Human heredity, 48(6), 1998, pp. 333-337
Authors:
FRANCO RF
ELION J
LAVINHA J
KRISHNAMOORTHY R
TAVELLA MH
ZAGO MA
Citation: Rf. Franco et al., HETEROGENEOUS ETHNIC DISTRIBUTION OF THE 844INS68 IN THE CYSTATHIONINE BETA-SYNTHASE GENE, Human heredity, 48(6), 1998, pp. 338-342
Authors:
SANGTHONGPITAG K
MOORE KR
LAPSYS NM
BAO F
BABU SR
FAIN PR
VERGE CF
Citation: K. Sangthongpitag et al., NO EVIDENCE FOR LINKAGE OF A NOVEL CA REPEAT POLYMORPHISM FOR APOPTOSIS ANTIGEN-1 (APO-1 OR FAS) WITH TYPE-I DIABETES IN A CAUCASIAN POPULATION, Human heredity, 48(6), 1998, pp. 343-345
Authors:
CAPEANS C
BLANCO MJ
LAREU MV
SALAS A
PINEIRO A
SANCHEZSALORIO M
CARRACEDO A
Citation: C. Capeans et al., (160)THR MUTATION IN THE RHODOPSIN GENE ASSOCIATED WITH RETINITIS-PIGMENTOSA, Human heredity, 48(5), 1998, pp. 237-240
Authors:
SOLDATOV NM
RAUDSEPP T
CHOWDHARY BP
Citation: Nm. Soldatov et al., REPETITIVE EXON 45 46-RELATED SEQUENCES OF HUMAN CA2+ CHANNEL ALPHA(1C) SUBUNIT GENE/, Human heredity, 48(5), 1998, pp. 241-244
Authors:
VANLANDEGHEM GF
BECKMAN LE
SIKSTROM C
SAHA N
KUCINSKAS V
BECKMAN L
Citation: Gf. Vanlandeghem et al., NEW DNA POLYMORPHISMS DEFINE ETHNICALLY DISTINCT HAPLOTYPES IN THE HUMAN TRANSFERRIN RECEPTOR GENE, Human heredity, 48(5), 1998, pp. 245-250
Authors:
ALLINGHAM RR
WIGGS JL
DAMJI KF
HERNDON L
YOUN J
TALLETT DA
JONES KH
DELBONO EA
REARDON M
HAINES JL
PERICAKVANCE MA
Citation: Rr. Allingham et al., ADULT-ONSET PRIMARY OPEN-ANGLE GLAUCOMA DOES NOT LOCALIZE TO CHROMOSOME 2CEN-Q13 IN NORTH-AMERICAN FAMILIES, Human heredity, 48(5), 1998, pp. 251-255
Authors:
HECIMOVIC S
BARISIC I
PAVELIC K
Citation: S. Hecimovic et al., DNA ANALYSIS OF THE FRAGILE-X-SYNDROME IN AN AT RISK PEDIATRIC POPULATION IN CROATIA - SIMPLE CLINICAL PRESELECTION CRITERIA CAN CONSIDERABLY IMPROVE THE COST-EFFECTIVENESS OF FRAGILE-X SCREENING STUDIES, Human heredity, 48(5), 1998, pp. 256-265
Authors:
LI WT
FANN CSJ
OTT J
Citation: Wt. Li et al., LOW-ORDER POLYNOMIAL TRENDS OF FEMALE-TO-MALE MAP DISTANCE RATIOS ALONG HUMAN-CHROMOSOMES, Human heredity, 48(5), 1998, pp. 266-270
Authors:
KAWASHIMA T
NOGUCHI E
ARINAMI T
KOBAYASHI K
OTSUKA F
HAMAGUCHI H
Citation: T. Kawashima et al., NO EVIDENCE FOR AN ASSOCIATION BETWEEN A VARIANT OF THE MAST-CELL CHYMASE GENE AND ATOPIC-DERMATITIS BASED ON CASE-CONTROL AND HAPLOTYPE-RELATIVE-RISK ANALYSES, Human heredity, 48(5), 1998, pp. 271-274
Authors:
LUCEK P
HANKE J
REICH J
SOLLA SA
OTT J
Citation: P. Lucek et al., MULTILOCUS NONPARAMETRIC LINKAGE ANALYSIS OF COMPLEX TRAIT LOCI WITH NEURAL NETWORKS, Human heredity, 48(5), 1998, pp. 275-284
Authors:
RAVNIKGLAVAC M
POTOCNIK U
KOZELJ M
KRIZMAN I
GLAVAC D
Citation: M. Ravnikglavac et al., A NOVEL IN FRAME DELETION OF CODONS 188-190 IN THE HMSH2 GENE OF A SLOVENIAN PATIENT WITH HEREDITARY NONPOLYPOSIS COLORECTAL-CANCER, Human heredity, 48(5), 1998, pp. 285-287
Authors:
PRICE JA
BOWDEN DW
HART TC
Citation: Ja. Price et al., IDENTIFICATION OF A CA TG REPEAT POLYMORPHISM PROXIMAL TO THE HUMAN DLX3 GENE/, Human heredity, 48(5), 1998, pp. 288-290
Authors:
POGODA T
METELSKAYA V
PEROVA N
LIMBORSKA S
Citation: T. Pogoda et al., DETECTION OF THE APO-B-3500 MUTATION IN A RUSSIAN FAMILY WITH CORONARY HEART-DISEASE, Human heredity, 48(5), 1998, pp. 291-292
Authors:
ASTOLFI P
CUCCIA M
MARTINETTI M
Citation: P. Astolfi et al., PARENTAL HLA GENES, HORMONE LEVEL AND OFFSPRING SEX-RATIOS - A REPLY TO JAMES LETTER, Human heredity, 48(5), 1998, pp. 293-294
Authors:
SPEER MC
VANCE JM
LENNONGRAHAM F
STAJICH JM
VILES KD
GILCHRIST JM
NIGRO V
MCMICHAEL R
CHUTKOW JG
BARTOLONI L
HORRIGAN SK
WESTBROOK CA
PERICAKVANCE MA
Citation: Mc. Speer et al., EXCLUSION OF IDENTIFIED LGMD1 LOCI FROM 4 DOMINANT LIMB-GIRDLE MUSCULAR-DYSTROPHY FAMILIES, Human heredity, 48(4), 1998, pp. 179-184
Authors:
BECKMAN L
SIKSTROM C
MIKELSAAR AV
KRUMINA A
AMBRASIENE D
KUCINSKAS V
BECKMAN G
Citation: L. Beckman et al., TRANSFERRIN VARIANTS AS MARKERS OF MIGRATIONS AND ADMIXTURE BETWEEN POPULATIONS IN THE BALTIC-SEA REGION, Human heredity, 48(4), 1998, pp. 185-191
Authors:
BOUANGA JC
MOUELE R
PREHU C
WAJCMAN H
FEINGOLD J
GALACTEROS F
Citation: Jc. Bouanga et al., GLUCOSE-6-PHOSPHATE-DEHYDROGENASE DEFICIENCY AND HOMOZYGOUS SICKLE-CELL DISEASE IN CONGO, Human heredity, 48(4), 1998, pp. 192-197
Authors:
LEDER RO
MANSBRIDGE JN
HALLMAYER J
HODGE SE
Citation: Ro. Leder et al., FAMILIAL PSORIASIS AND HLA-B - UNAMBIGUOUS SUPPORT FOR LINKAGE IN 97 PUBLISHED FAMILIES, Human heredity, 48(4), 1998, pp. 198-211
Authors:
SHINKAI T
OHMORI O
KOJIMA H
TERAO T
SUZUKI T
ABE K
Citation: T. Shinkai et al., NEGATIVE ASSOCIATION BETWEEN T102C POLYMORPHISM OF THE 5-HT2A RECEPTOR GENE AND SCHIZOPHRENIA IN JAPAN, Human heredity, 48(4), 1998, pp. 212-215
Authors:
LOBATO MN
ALEDO R
MESEGUER A
Citation: Mn. Lobato et al., HIGH VARIABILITY OF CYP21 GENE REARRANGEMENTS IN SPANISH PATIENTS WITH CLASSIC FORM OF CONGENITAL ADRENAL-HYPERPLASIA, Human heredity, 48(4), 1998, pp. 216-225