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Clinical Genetics Volume 72 Issue 5

2013
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2011
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2009
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2008
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2007
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1995
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1994
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1993
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1992
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1991
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1990
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1989
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1988
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1987
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1986
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1985
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1984
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1983
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1982
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1981
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1980
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1979
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1978
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1977
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1976
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1975
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1974
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1973
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1972
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1971
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1970
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DMPK -associated myotonic dystrophy and CTG repeats in Alabama African Americans

Acton,; Rivers,; Watson,; Oh,

Follow Clinical Genetics , Volume 72 (5) Wiley – Nov 1, 2007
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A novel DFNA5 mutation, IVS8+4 A>G, in the splice donor site of intron 8 causes late-onset non-syndromic hearing loss in a Chinese family

Cheng,; Han,; Dai,; Sun,; Tao,; Sun,; Yan,; Qin,; Wang,; Ouyang,; Yang,; Cao,; Feng,; Du,; Zhang,; Zhai,; Yang,; Liu,; He,; Yuan,

Follow Clinical Genetics , Volume 72 (5) Wiley – Nov 1, 2007
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Genetics of Noonan syndrome – a new gene, and the search is still on

Stein,

Follow Clinical Genetics , Volume 72 (5) Wiley – Nov 1, 2007
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Formalin-fixed paraffin-embedded clinical tissues show spurious copy number changes in array-CGH profiles

Mc Sherry,; Mc Goldrick,; Kay,; Hopkins,; Gallagher,; Dervan,

Follow Clinical Genetics , Volume 72 (5) Wiley – Nov 1, 2007
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GFAP mutations and polymorphisms in 13 unrelated Italian patients affected by Alexander disease

Caroli,; Biancheri,; Seri,; Rossi,; Pessagno,; Bugiani,; Corsolini,; Savasta,; Romano,; Antonelli,; Romano,; Pareyson,; Gambero,; Uziel,; Ravazzolo,; Ceccherini,; Filocamo,

Follow Clinical Genetics , Volume 72 (5) Wiley – Nov 1, 2007
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The role of common genetic risk variants in Parkinson disease

Tan,

Follow Clinical Genetics , Volume 72 (5) Wiley – Nov 1, 2007
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Prenatal diagnosis of Miller-Dieker syndrome by ultrasound and molecular cytogenetic analysis

Lenzini, Elisabetta; D’Ottavio, Giuseppina; Città, Angelo; Benussi, Daniela Gambel; Petix, Vincenzo; Pecile, Vanna

Follow Clinical Genetics , Volume 72 (5) Wiley – Nov 1, 2007
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A disease causing deletion of 29 base pairs in intron 15 in the MKS1 gene is highly associated with the campomelic variant of the Meckel–Gruber syndrome

Auber,; Burfeind,; Herold,; Schoner,; Simson,; Rauskolb,; Rehder,

Follow Clinical Genetics , Volume 72 (5) Wiley – Nov 1, 2007
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Pallister–Killian syndrome: tetrasomy of 12pter→12p11.22 in a boy with an analphoid, inverted duplicated marker chromosome

Huang,; Isabel de Michelena,; Leon,; Maher,; McClure,; Milunsky,

Follow Clinical Genetics , Volume 72 (5) Wiley – Nov 1, 2007
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Colorectal cancer survivors undergoing genetic testing for hereditary non-polyposis colorectal cancer: motivational factors and psychosocial functioning

Esplen,; Madlensky,; Aronson,; Rothenmund,; Gallinger,; Butler,; Toner,; Wong,; Manno,; McLaughlin,

Follow Clinical Genetics , Volume 72 (5) Wiley – Nov 1, 2007

Clinical Genetics Volume 72 Issue 5

DMPK -associated myotonic dystrophy and CTG repeats in Alabama African Americans

Acton,; Rivers,; Watson,; Oh,

Follow Clinical Genetics , Volume 72 (5) Wiley – Nov 1, 2007

A novel DFNA5 mutation, IVS8+4 A>G, in the splice donor site of intron 8 causes late-onset non-syndromic hearing loss in a Chinese family

Cheng,; Han,; Dai,; Sun,; Tao,; Sun,; Yan,; Qin,; Wang,; Ouyang,; Yang,; Cao,; Feng,; Du,; Zhang,; Zhai,; Yang,; Liu,; He,; Yuan,

Follow Clinical Genetics , Volume 72 (5) Wiley – Nov 1, 2007

Genetics of Noonan syndrome – a new gene, and the search is still on

Stein,

Follow Clinical Genetics , Volume 72 (5) Wiley – Nov 1, 2007

Formalin-fixed paraffin-embedded clinical tissues show spurious copy number changes in array-CGH profiles

Mc Sherry,; Mc Goldrick,; Kay,; Hopkins,; Gallagher,; Dervan,

Follow Clinical Genetics , Volume 72 (5) Wiley – Nov 1, 2007

GFAP mutations and polymorphisms in 13 unrelated Italian patients affected by Alexander disease

Caroli,; Biancheri,; Seri,; Rossi,; Pessagno,; Bugiani,; Corsolini,; Savasta,; Romano,; Antonelli,; Romano,; Pareyson,; Gambero,; Uziel,; Ravazzolo,; Ceccherini,; Filocamo,

Follow Clinical Genetics , Volume 72 (5) Wiley – Nov 1, 2007

The role of common genetic risk variants in Parkinson disease

Tan,

Follow Clinical Genetics , Volume 72 (5) Wiley – Nov 1, 2007

Prenatal diagnosis of Miller-Dieker syndrome by ultrasound and molecular cytogenetic analysis

Lenzini, Elisabetta; D’Ottavio, Giuseppina; Città, Angelo; Benussi, Daniela Gambel; Petix, Vincenzo; Pecile, Vanna

Follow Clinical Genetics , Volume 72 (5) Wiley – Nov 1, 2007

A disease causing deletion of 29 base pairs in intron 15 in the MKS1 gene is highly associated with the campomelic variant of the Meckel–Gruber syndrome

Auber,; Burfeind,; Herold,; Schoner,; Simson,; Rauskolb,; Rehder,

Follow Clinical Genetics , Volume 72 (5) Wiley – Nov 1, 2007

Pallister–Killian syndrome: tetrasomy of 12pter→12p11.22 in a boy with an analphoid, inverted duplicated marker chromosome

Huang,; Isabel de Michelena,; Leon,; Maher,; McClure,; Milunsky,

Follow Clinical Genetics , Volume 72 (5) Wiley – Nov 1, 2007

Colorectal cancer survivors undergoing genetic testing for hereditary non-polyposis colorectal cancer: motivational factors and psychosocial functioning

Esplen,; Madlensky,; Aronson,; Rothenmund,; Gallinger,; Butler,; Toner,; Wong,; Manno,; McLaughlin,

Follow Clinical Genetics , Volume 72 (5) Wiley – Nov 1, 2007

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Clinical Genetics Volume 72 Issue 5

1 - 10 of 18 articles

Acton,; Rivers,; Watson,; Oh,

Follow Clinical Genetics , Volume 72 (5) Wiley – Nov 1, 2007

Cheng,; Han,; Dai,; Sun,; Tao,; Sun,; Yan,; Qin,; Wang,; Ouyang,; Yang,; Cao,; Feng,; Du,; Zhang,; Zhai,; Yang,; Liu,; He,; Yuan,

Follow Clinical Genetics , Volume 72 (5) Wiley – Nov 1, 2007

Follow Clinical Genetics , Volume 72 (5) Wiley – Nov 1, 2007

Mc Sherry,; Mc Goldrick,; Kay,; Hopkins,; Gallagher,; Dervan,

Follow Clinical Genetics , Volume 72 (5) Wiley – Nov 1, 2007

Caroli,; Biancheri,; Seri,; Rossi,; Pessagno,; Bugiani,; Corsolini,; Savasta,; Romano,; Antonelli,; Romano,; Pareyson,; Gambero,; Uziel,; Ravazzolo,; Ceccherini,; Filocamo,

Follow Clinical Genetics , Volume 72 (5) Wiley – Nov 1, 2007

Follow Clinical Genetics , Volume 72 (5) Wiley – Nov 1, 2007

Lenzini, Elisabetta; D’Ottavio, Giuseppina; Città, Angelo; Benussi, Daniela Gambel; Petix, Vincenzo; Pecile, Vanna

Follow Clinical Genetics , Volume 72 (5) Wiley – Nov 1, 2007

Auber,; Burfeind,; Herold,; Schoner,; Simson,; Rauskolb,; Rehder,

Follow Clinical Genetics , Volume 72 (5) Wiley – Nov 1, 2007

Huang,; Isabel de Michelena,; Leon,; Maher,; McClure,; Milunsky,

Follow Clinical Genetics , Volume 72 (5) Wiley – Nov 1, 2007

Esplen,; Madlensky,; Aronson,; Rothenmund,; Gallinger,; Butler,; Toner,; Wong,; Manno,; McLaughlin,

Follow Clinical Genetics , Volume 72 (5) Wiley – Nov 1, 2007