New! Learn more about the all new DeepDyve personalized home page where you can quickly skim your favorite journals all from one place

Clinical Genetics Volume 64 Issue 3

2013
- Volume 83
2012
- Volume 82
- Volume 81
2011
- Volume 80
- Volume 79
2010
- Volume 78
- Volume 77
2009
- Volume 76
- Volume 75
2008
- Volume 74
- Volume 73
2007
- Volume 72
- Volume 71
2006
- Volume 70
- Volume 69
2005
- Volume 68
- Volume 67
2004
- Volume 66
- Volume 65
2003
- Volume 64
- Volume 63
2002
- Volume 62
- Volume 61
2001
- Volume 60
- Volume 59
2000
- Volume 58
- Volume 57
1999
- Volume 57
  - S1 (Apr)
- Volume 56
- Volume 55
1998
- Volume 54
- Volume 53
1997
- Volume 52
- Volume 51
1996
- Volume 50
- Volume 49
1995
- Volume 48
- Volume 47
1994
- Volume 46
- Volume 45
1993
- Volume 44
- Volume 43
1992
- Volume 42
- Volume 41
1991
- Volume 40
- Volume 39
1990
- Volume 38
- Volume 37
1989
- Volume 36
- Volume 35
1988
- Volume 34
- Volume 33
1987
- Volume 32
- Volume 31
1986
- Volume 30
- Volume 29
1985
- Volume 28
- Volume 27
1984
- Volume 26
- Volume 25
1983
- Volume 24
- Volume 23
1982
- Volume 22
- Volume 21
1981
- Volume 20
- Volume 19
1980
- Volume 18
- Volume 17
1979
- Volume 16
- Volume 15
1978
- Volume 14
- Volume 13
1977
- Volume 12
- Volume 11
1976
- Volume 10
- Volume 9
1975
- Volume 8
- Volume 7
1974
- Volume 6
- Volume 5
1973
- Volume 4
1972
- Volume 3
1971
- Volume 2
1970
- Volume 1

Bookmark
More Like This q7VCv4rPND Rentable

Association of autism severity with a monoamine oxidase A functional polymorphism

Cohen, IL; Liu, X; Schutz, C; White, BN; Jenkins, EC; Brown, WT; Holden, JJA

Follow Clinical Genetics , Volume 64 (3) Wiley – Sep 1, 2003
Bookmark
More Like This 79vq78QMhE Rentable

Rare compound heterozygosity for IVS2 +1G>A and R170P in an Italian patient with Gaucher disease type 1

Concolino, D.; Mussari, A.; Filocamo, M.; Strisciuglio, P.

Follow Clinical Genetics , Volume 64 (3) Wiley – Sep 1, 2003
Bookmark
More Like This X0uNJfg8Rk Rentable

No evidence of submicroscopic deletion or segmental uniparental disomy within the candidate regions 7p11.2-p13 and 7q31-qter in a series of non-uniparental disomy Silver–Russell syndrome cases

Riegel, M.; Baumer, A.; Schinzel, A.

Follow Clinical Genetics , Volume 64 (3) Wiley – Sep 1, 2003
Bookmark
More Like This MacfbddLlg Rentable

Two new point mutations of the SRY gene identified in two Italian 46,XY females with gonadal dysgenesis

Baldazzi, L.; Nicolettic, A.; Gennari, M.; Barbaro, M.; Pirazzoli, P.; Cicognani, A.; Cacciari, E.

Follow Clinical Genetics , Volume 64 (3) Wiley – Sep 1, 2003
Bookmark
More Like This sJPGNi99RB Rentable

Germline hMLH1 promoter mutation in a Newfoundland HNPCC kindred

Green, RC; Green, AG; Simms, M; Pater, A; Robb, JD; Green, JS

Follow Clinical Genetics , Volume 64 (3) Wiley – Sep 1, 2003
Bookmark
More Like This xizUHdKAX6 Rentable

Personal theories of inheritance, coping strategies, risk perception and engagement in hereditary non-polyposis colon cancer families offered genetic testing

McAllister, M

Follow Clinical Genetics , Volume 64 (3) Wiley – Sep 1, 2003
Bookmark
More Like This G9Jr0UZWM4 Rentable

ROR2 is mutated in hereditary brachydactyly with nail dysplasia, but not in Sorsby syndrome

Bacchelli, C.; Wilson, L. C.; Cook, J. A.; Winter, R. M.; Goodman, F. R.

Follow Clinical Genetics , Volume 64 (3) Wiley – Sep 1, 2003
Bookmark
More Like This YI7v98Kgts Rentable

Low mutation rate of hMSH2 and hMLH1 in Taiwanese hereditary non-polyposis colorectal cancer

Wei, S-C; Yu, C-Y; Tsai-Wu, J-J; Su, Y-N; Sheu, J-C; Wu, C-HH; Wang, C-Y; Wong, J-M

Follow Clinical Genetics , Volume 64 (3) Wiley – Sep 1, 2003
Bookmark
More Like This ZaXeMb0l8e Rentable

Identification of three novel SEDL mutations, including mutation in the rare, non-canonical splice site of exon 4

Shaw, MA; Brunetti-Pierri, N; Kádasi, L; Kovácová, V; Van Maldergem, L; De Brasi, D; Salerno, M; Gécz, J

Follow Clinical Genetics , Volume 64 (3) Wiley – Sep 1, 2003
Bookmark
More Like This QzCawV59YR Rentable

Pure partial trisomy of 2q22-q23 secondary to a paternally inherited direct insertion: a rare duplication

Farrell, S.A.; Sajoo, A.; Maybury, D.; Speevak, M.D.

Follow Clinical Genetics , Volume 64 (3) Wiley – Sep 1, 2003

Clinical Genetics Volume 64 Issue 3

Association of autism severity with a monoamine oxidase A functional polymorphism

Cohen, IL; Liu, X; Schutz, C; White, BN; Jenkins, EC; Brown, WT; Holden, JJA

Follow Clinical Genetics , Volume 64 (3) Wiley – Sep 1, 2003

Rare compound heterozygosity for IVS2 +1G>A and R170P in an Italian patient with Gaucher disease type 1

Concolino, D.; Mussari, A.; Filocamo, M.; Strisciuglio, P.

Follow Clinical Genetics , Volume 64 (3) Wiley – Sep 1, 2003

No evidence of submicroscopic deletion or segmental uniparental disomy within the candidate regions 7p11.2-p13 and 7q31-qter in a series of non-uniparental disomy Silver–Russell syndrome cases

Riegel, M.; Baumer, A.; Schinzel, A.

Follow Clinical Genetics , Volume 64 (3) Wiley – Sep 1, 2003

Two new point mutations of the SRY gene identified in two Italian 46,XY females with gonadal dysgenesis

Baldazzi, L.; Nicolettic, A.; Gennari, M.; Barbaro, M.; Pirazzoli, P.; Cicognani, A.; Cacciari, E.

Follow Clinical Genetics , Volume 64 (3) Wiley – Sep 1, 2003

Germline hMLH1 promoter mutation in a Newfoundland HNPCC kindred

Green, RC; Green, AG; Simms, M; Pater, A; Robb, JD; Green, JS

Follow Clinical Genetics , Volume 64 (3) Wiley – Sep 1, 2003

Personal theories of inheritance, coping strategies, risk perception and engagement in hereditary non-polyposis colon cancer families offered genetic testing

McAllister, M

Follow Clinical Genetics , Volume 64 (3) Wiley – Sep 1, 2003

ROR2 is mutated in hereditary brachydactyly with nail dysplasia, but not in Sorsby syndrome

Bacchelli, C.; Wilson, L. C.; Cook, J. A.; Winter, R. M.; Goodman, F. R.

Follow Clinical Genetics , Volume 64 (3) Wiley – Sep 1, 2003

Low mutation rate of hMSH2 and hMLH1 in Taiwanese hereditary non-polyposis colorectal cancer

Wei, S-C; Yu, C-Y; Tsai-Wu, J-J; Su, Y-N; Sheu, J-C; Wu, C-HH; Wang, C-Y; Wong, J-M

Follow Clinical Genetics , Volume 64 (3) Wiley – Sep 1, 2003

Identification of three novel SEDL mutations, including mutation in the rare, non-canonical splice site of exon 4

Shaw, MA; Brunetti-Pierri, N; Kádasi, L; Kovácová, V; Van Maldergem, L; De Brasi, D; Salerno, M; Gécz, J

Follow Clinical Genetics , Volume 64 (3) Wiley – Sep 1, 2003

Pure partial trisomy of 2q22-q23 secondary to a paternally inherited direct insertion: a rare duplication

Farrell, S.A.; Sajoo, A.; Maybury, D.; Speevak, M.D.

Follow Clinical Genetics , Volume 64 (3) Wiley – Sep 1, 2003

Advanced Filters:

Specific Data Sources:

Clinical Genetics Volume 64 Issue 3

1 - 10 of 16 articles

Cohen, IL; Liu, X; Schutz, C; White, BN; Jenkins, EC; Brown, WT; Holden, JJA

Follow Clinical Genetics , Volume 64 (3) Wiley – Sep 1, 2003

Concolino, D.; Mussari, A.; Filocamo, M.; Strisciuglio, P.

Follow Clinical Genetics , Volume 64 (3) Wiley – Sep 1, 2003

Riegel, M.; Baumer, A.; Schinzel, A.

Follow Clinical Genetics , Volume 64 (3) Wiley – Sep 1, 2003

Baldazzi, L.; Nicolettic, A.; Gennari, M.; Barbaro, M.; Pirazzoli, P.; Cicognani, A.; Cacciari, E.

Follow Clinical Genetics , Volume 64 (3) Wiley – Sep 1, 2003

Green, RC; Green, AG; Simms, M; Pater, A; Robb, JD; Green, JS

Follow Clinical Genetics , Volume 64 (3) Wiley – Sep 1, 2003

Follow Clinical Genetics , Volume 64 (3) Wiley – Sep 1, 2003

Bacchelli, C.; Wilson, L. C.; Cook, J. A.; Winter, R. M.; Goodman, F. R.

Follow Clinical Genetics , Volume 64 (3) Wiley – Sep 1, 2003

Wei, S-C; Yu, C-Y; Tsai-Wu, J-J; Su, Y-N; Sheu, J-C; Wu, C-HH; Wang, C-Y; Wong, J-M

Follow Clinical Genetics , Volume 64 (3) Wiley – Sep 1, 2003

Shaw, MA; Brunetti-Pierri, N; Kádasi, L; Kovácová, V; Van Maldergem, L; De Brasi, D; Salerno, M; Gécz, J

Follow Clinical Genetics , Volume 64 (3) Wiley – Sep 1, 2003

Farrell, S.A.; Sajoo, A.; Maybury, D.; Speevak, M.D.

Follow Clinical Genetics , Volume 64 (3) Wiley – Sep 1, 2003