AAAAAA

   
Results: 1-10 |
Results: 10
NOVEL CYSTIC-FIBROSIS MUTATION INVOLVING DELETION OF EXON 14B THROUGHEXON-18 (GF20KBDEL 14B-18) IN A CYSTIC-FIBROSIS PATIENT OF GERMAN DESCENT FROM UPSTATE NEW-YORK
Authors: SHRIMPTON AE BOROWITZ D
Citation: Ae. Shrimpton et D. Borowitz, NOVEL CYSTIC-FIBROSIS MUTATION INVOLVING DELETION OF EXON 14B THROUGHEXON-18 (GF20KBDEL 14B-18) IN A CYSTIC-FIBROSIS PATIENT OF GERMAN DESCENT FROM UPSTATE NEW-YORK, Human mutation, 1998, pp. 330-331
MAPPING A GENE (MRXS9) FOR X-LINKED RETARDATION, MICROCEPHALY AND VARIABLE STATURE TO XQ12-Q21.31
Authors: SHRIMPTON AE DALY K HOO J
Citation: Ae. Shrimpton et al., MAPPING A GENE (MRXS9) FOR X-LINKED RETARDATION, MICROCEPHALY AND VARIABLE STATURE TO XQ12-Q21.31, The American journal of pathology, 153(5), 1998, pp. 13-13
CHARACTERIZATION OF A FAMILIAL NEURODEGENERATIVE DISORDER ASSOCIATED WITH NEUROSERPIN INCLUSION-BODIES
Authors: SHRIMPTON AE DAVIS R HOLOHAN P
Citation: Ae. Shrimpton et al., CHARACTERIZATION OF A FAMILIAL NEURODEGENERATIVE DISORDER ASSOCIATED WITH NEUROSERPIN INCLUSION-BODIES, The American journal of pathology, 153(5), 1998, pp. 14-14
UNTITLED
Authors: SHRIMPTON AE HICKS K
Citation: Ae. Shrimpton et K. Hicks, UNTITLED, Molecular diagnosis, 2(2), 1997, pp. 160-160
CYSTIC-FIBROSIS MUTATION FREQUENCIES IN UPSTATE NEW-YORK
Authors: SHRIMPTON AE BOROWITZ D SWENDER P
Citation: Ae. Shrimpton et al., CYSTIC-FIBROSIS MUTATION FREQUENCIES IN UPSTATE NEW-YORK, Human mutation, 10(6), 1997, pp. 436-442
DETECTION OF CLONAL REARRANGEMENTS OF T-CELL RECEPTOR-GAMMA CHAIN GENES
Authors: UNER AH LAMBERSON CM HUTCHISON RE SHRIMPTON AE
Citation: Ah. Uner et al., DETECTION OF CLONAL REARRANGEMENTS OF T-CELL RECEPTOR-GAMMA CHAIN GENES, The American journal of pathology, 151(5), 1997, pp. 1-1
FRAGILE-X-SYNDROME MOLECULAR-DETECTION
Authors: SHRIMPTON AE HICKS K LAMBERSON CM
Citation: Ae. Shrimpton et al., FRAGILE-X-SYNDROME MOLECULAR-DETECTION, The American journal of pathology, 151(5), 1997, pp. 3-3
A MUTATION IN CFTR PRODUCES DIFFERENT PHENOTYPES DEPENDING ON CHROMOSOMAL BACKGROUND
Authors: KIESEWETTER S MACEK M DAVIS C CURRISTIN SM CHU CS GRAHAM C SHRIMPTON AE CASHMAN SM TSUI LC MICKLE J AMOS J HIGHSMITH WE SHUBER A WITT DR CRYSTAL RG CUTTING GR
Citation: S. Kiesewetter et al., A MUTATION IN CFTR PRODUCES DIFFERENT PHENOTYPES DEPENDING ON CHROMOSOMAL BACKGROUND, Nature genetics, 5(3), 1993, pp. 274-278
PRESYMPTOMATIC TESTING FOR AUTOSOMAL-DOMINANT SPINOCEREBELLAR ATAXIA TYPE-1
Authors: SHRIMPTON AE DAVIDSON R MACDONALD N BROCK DJH
Citation: Ae. Shrimpton et al., PRESYMPTOMATIC TESTING FOR AUTOSOMAL-DOMINANT SPINOCEREBELLAR ATAXIA TYPE-1, Journal of Medical Genetics, 30(7), 1993, pp. 616-617
THE CFTR MUTATION R117H PRODUCES DIFFERENT PHENOTYPES DEPENDING ON GENETIC BACKGROUND
Authors: KIESEWETTER S MACEK M CURRISTIN S CHU C GRAHAM C SHRIMPTON AE DEARCE M ZIELENSKI J MICKLE J AMOS J HIGHSMITH WE SHUBER A WITT D CRYSTAL RG CUTTING GR
Citation: S. Kiesewetter et al., THE CFTR MUTATION R117H PRODUCES DIFFERENT PHENOTYPES DEPENDING ON GENETIC BACKGROUND, American journal of human genetics, 53(3), 1993, pp. 86-86
Risultati: 1-10 |