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Inuit
ARPKD (2003)
CMMRD PMS2 (2015)
CPT1A P479L (2010)
Determinants of health review (2003)
Cholestasis (2009)
Fanconi (2005)
Sucrase-isomaltase deficiency (2015)
First Nations
Acro-renal-uterine-mandibular syndrome (2000)
Allgrove syndrome (1991)
Allgrove syndrome (1996)
AOA2 (2016)
Bardet-Biedl (2010)
BRCA1 (2002)
CARD11 immunodeficiency (2018)
COFS/Cockayne (1997)
COFS/Cockayne (2000)
Congenital analbuminemia (2012)
CPT1A P479L (2009)
Cree leukodystrophy/vWMD/CACH (2010)
Epidermolysis bullosa-pyloric atresia (2001)
GA1 (1995)
GA1 (2002)
GA1 (2005)
GA1 (2006)
Hereditary multiple exostoses (1993)
Hypertonic muscular dystrophy (1994)
Hypertonic muscular dystrophy (2001)
Hypertonic muscular dystrophy (2011)
Improving aboriginal health (2009)
Leukoencephalopathy -abstract only (1988)
LGMD2B (1996)
LGMD2B (1999)
Long QT syndrome (2011)
Metabolic diseases (1991)
Microcephaly-micromelia syndrome (2017)
MOTA (2007)
MOTA (2011)
Nephronophthisis (2007)
Neurodegenerative (2009)
PRUNE1 (2016)
PRUNE1 (2018)
Pyruvate carboxylase (1998)
Recurrent acute necrotizing encephalopathy (2011)
Ritscher-Schinzel (1995)
Ritscher-Schinzel (2013)
Ritscher-Schinzel (2016)
SCID (2000)
SCID (2018)
SCID IKBKB (2013)
Sideroblastic anemia (2020)
TAPVD (1996)
Type 2 diabetes HNF-1alpha (2002)
Hutterite
Androgen insensitivity syndrome (1995)
ARVC (2013)
ARVC (2014)
Bardet-Biedl syndrome (2010)
Beaulieu-Boycott-Innes syndrome (2010)
Bowen-Conradi (2003)
Bowen-Conradi (2005)
Bowen-Conradi (2009)
Bowen-Conradi (2015)
Cardiomyopathy, DCMA (2005)
Cardiomyopathy, LEMD2 (2019)
Carrier frequencies (2012)
CASS (2015)
Cataract (1987)
Clinical genetics and the Hutterite population (2008)
Congenital hypothyroidism (1999)
CPT1 (2000)
CPT1 (2001)
CSPP1 ciliopathy (2013)
Cystic fibrosis (2019)
Diagnostic chip (2016)
Dysequilibrium syndrome (2005)
Dysequilibrium syndrome (2005)
Ectodermal dysplasia, WNT10A (2009)
ID, TECR (2011)
JSRD (2011)
JSRD (2016)
JSRD (2018)
LGMD2H and LGMD2I combined (2005)
Muscular dystrophy (1976)
Myopathy/ID/ataxia, TRAPPC11 (2013)
Restrictive dermopathy (2012)
Treacher Collins (2013)
Mennonite
17 alpha-hydroxylase/17,20-lyase deficiency (1989)
17-hydroxylase and 17,20-desmolase def. (1989)
Ataxia-telangiectasia (2012)
Ataxia-telangiectasia (2014)
Ataxia-telangiectasia (2015)
Ataxia-telangiectasia, cancer treatment (2009)
Chudley-McCullough (1997)
Chudley-McCullough syndrome (2012)
Cleft palate and ankyloglossia, TXB22 (2001)
CODAS syndrome (2001)
CODAS syndrome (2015)
CSNB, X-linked (2000)
Disease heritage (2008)
Dysosteosclerosis (2007)
Fanconi anemia (2012)
FAP (2008)
HCM, MYBPC3 (1998)
HPP, ERT (2012)
HPP, perinatal (2012)
Lynch (2008)
MARCH syndrome (2017)
Pontocerebellar hypoplasia, TOE7 (2013)
Restrictive dermopathy (2012)
SAMS syndrome (1998)
SAMS syndrome (2013)
SCID (2003)
SCID (2014)
SCID, ADA (1995)
SCID, NBS (2018)
SCID, ZAP70 (2016)
Torkelson syndrome (1994)
French-Canadian
AR disease in Saguenay-Lac-Saint-Jean (2022)
French-Canadian review (2005)
French-Canadian Zellweger (2012)
Saguenay-Lac-Saint-Jean (2021)
Newfoundland
Hereditary diffuse gastric cancer, CDH1 (2007)
Jewish
APC polymorphism AJ (2013)
Carrier screening (2006)
Carrier screening (2008)
Carrier screening (2009)
Carrier screening, CCMG (2016)
Genetic profile (2001)
Hearing loss, OTOF AJ (2016)
Israel genetic testing (2009)
Lynch, MSH2 AJ (2008)
Retinitis pigmentosa AJ (2020)
Pakistani
MICRO syndrome (2001)
MICRO syndrome (2004)
Palestinian
AR diseases (1997)
AR diseases, molecular basis (2002)
Hydrocephalus (1997)
Hydrocephalus, CCDC88C (2012)
Walker-Warburg syndrome (2008)
Walker-Warburg syndrome (2015)
Icelandic
Breast cancer, BARD1 (2006)
Breast cancer, BRCA2 (1998)
Ovarian cancer, BRIP1 (2011)
Saudi Arabian
Al-Awadi syndrome (1985)
Al-Awadi syndrome (2007)
Al-Awadi syndrome (2013)
AR genetic disorders (2012)
Dutch
FHM, PRRT2 (2014)
FHM and epilepsy (1997)
FHM and epilepsy, ATP1A2 (2003)
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