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Results: 1-8 |
Results: 8
A LOCUS FOR AUTOSOMAL RECESSIVE HYPODONTIA WITH ASSOCIATED DENTAL ANOMALIES MAPS TO CHROMOSOME 16Q12.1
Authors: AHMAD W BRANCOLINI V ULHAQUE MF LAM H ULHAQUE S HAIDER M MAIMON A AITA VM OWEN J BROWN D ZEGARELLI DJ AHMAD M OTT J CHRISTIANO AM
Citation: W. Ahmad et al., A LOCUS FOR AUTOSOMAL RECESSIVE HYPODONTIA WITH ASSOCIATED DENTAL ANOMALIES MAPS TO CHROMOSOME 16Q12.1, American journal of human genetics, 62(4), 1998, pp. 987-991
A GENOME-WIDE SCAN FOR BIPOLAR AFFECTIVE-DISORDER
Authors: LIU J AITA VM KNOWLES JA TERWILLIGER JD BALTAZAR R GRUNN A YUN O LOTH JE ALEXANDER JR LERER B ENDICOTT J WANG Z PENCHASZADEH G GILLIAM TC BARON M
Citation: J. Liu et al., A GENOME-WIDE SCAN FOR BIPOLAR AFFECTIVE-DISORDER, American journal of medical genetics, 81(6), 1998, pp. 462-462
A FOLLOW-UP LINKAGE ANALYSIS OF CHROMOSOME-21 CONTINUES TO PROVIDE EVIDENCE FOR A PUTATIVE BIPOLAR AFFECTIVE-DISORDER LOCUS
Authors: AITA VM LIU J TERWILLIGER JD BALTAZAR R GRUNN A LOTH JE ALEXANDER JR LERER B ENDICOTT H WANG Z PENCHASZADEH G KNOWLES JA GILLIAM TC BARON M
Citation: Vm. Aita et al., A FOLLOW-UP LINKAGE ANALYSIS OF CHROMOSOME-21 CONTINUES TO PROVIDE EVIDENCE FOR A PUTATIVE BIPOLAR AFFECTIVE-DISORDER LOCUS, American journal of medical genetics, 81(6), 1998, pp. 476-476
ALOPECIA UNIVERSALIS ASSOCIATED WITH A MUTATION IN THE HUMAN HAIRLESSGENE
Authors: AHMAD W HAQUE WFU BRANCOLINI V TSOU HC HAQUE SU LAM H AITA VM OWEN J DEBLAQUIERE M FRANK J CSERHALMIFRIEDMAN PB LEASK A MCGRATH JA PEACOCKE M AHMAD M OTT J CHRISTIANO AM
Citation: W. Ahmad et al., ALOPECIA UNIVERSALIS ASSOCIATED WITH A MUTATION IN THE HUMAN HAIRLESSGENE, Science, 279(5351), 1998, pp. 720-724
CONGENITAL ERYTHROPOIETIC PORPHYRIA - C73R IS A HOTSPOT MUTATION IN THE UROPORPHYRINOGEN-III SYNTHASE GENE
Authors: LAM HM FRANK J WANG XH AITA VM JUGERT FK KALKA K GOERZ G MERK HF POHFITZPATRICK B CHRISTIANO AM
Citation: Hm. Lam et al., CONGENITAL ERYTHROPOIETIC PORPHYRIA - C73R IS A HOTSPOT MUTATION IN THE UROPORPHYRINOGEN-III SYNTHASE GENE, Journal of investigative dermatology, 110(4), 1998, pp. 615-615
C73R IS A HOTSPOT MUTATION IN THE UROPORPHYRINOGEN III SYNTHASE GENE IN CONGENITAL ERYTHROPOIETIC PORPHYRIA
Authors: FRANK J WANG X LAM HM AITA VM JUGERT FK GOERZ G MERK HF POHFITZPATRICK MB CHRISTIANO AM
Citation: J. Frank et al., C73R IS A HOTSPOT MUTATION IN THE UROPORPHYRINOGEN III SYNTHASE GENE IN CONGENITAL ERYTHROPOIETIC PORPHYRIA, Annals of Human Genetics, 62, 1998, pp. 225-230
PROGRESS IN A GENOME-WIDE SEARCH FOR GENETIC-FACTORS FOR BIPOLAR DISORDER
Authors: LIU J AITA VM WANG Z KNOWLES JA TERWILLIGER J MATIS TC GRUNN A RANTA S ENDICOTT J LOTH JE LERER B ALEXANDER JR OTT J GILLIAM TC BARON M
Citation: J. Liu et al., PROGRESS IN A GENOME-WIDE SEARCH FOR GENETIC-FACTORS FOR BIPOLAR DISORDER, American journal of medical genetics, 74(6), 1997, pp. 590-590
ANALYSIS FOR LINKAGE TO BIPOLAR AFFECTIVE-DISORDER IN SELECT CHROMOSOMAL REGIONS - 4P, 18, AND XQ24-28
Authors: AITA VM KNOWLES JA TERWILLIGER J WANG Z LIU J ENDICOTT J LOTH JE LERER B ALEXANDER JR GRUNN A PENCHASZADEH G BARON M GILLIAM TC
Citation: Vm. Aita et al., ANALYSIS FOR LINKAGE TO BIPOLAR AFFECTIVE-DISORDER IN SELECT CHROMOSOMAL REGIONS - 4P, 18, AND XQ24-28, American journal of human genetics, 61(4), 1997, pp. 2324-2324
Risultati: 1-8 |