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Imprinting of a RING Zinc-Finger Encoding Gene in the Mouse Chromosome Region Homologous to the Prader-Willi Syndrome Genetic Region

Human molecular genetics, 1999-05, Vol.8 (5), p.795-803

1999

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Polycystic ovaries and premature male pattern baldness are associated with one allele of the steroid metabolism gene CYP17

Human molecular genetics, 1994-10, Vol.3 (10), p.1873-1876

1994

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Evidence for a single gene effect causing polycystic ovaries and male pattern baldness

Clinical endocrinology (Oxford), 1993-06, Vol.38 (6), p.653-658

1993

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Fibroid embolisation: a technique not without significant complications

BJOG : an international journal of obstetrics and gynaecology, 2000-09, Vol.107 (9), p.1166-1170

2000

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Alpha-B Crystallin Gene ( CRYAB) Mutation Causes Dominant Congenital Posterior Polar Cataract in Humans

American journal of human genetics, 2001-11, Vol.69 (5), p.1141-1145

2001

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A study to evaluate serum and urinary hormone levels following short and long term administration of two regimens of progesterone cream in postmenopausal women

BJOG : an international journal of obstetrics and gynaecology, 2000-06, Vol.107 (6), p.722-726

2000

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Identification of novel polymorphisms in the β7 integrin gene: family-based association studies in inflammatory bowel disease

Genes and immunity, 2001-12, Vol.2 (8), p.455-460

2001

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Microdeletions within 22q11 associated with sporadic and familial DiGeorge syndrome

Genomics (San Diego, Calif.), 1991-05, Vol.10 (1), p.201-206

1991

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Molecular genetic study of the frequency of monosomy 22q11 in DiGeorge syndrome

American journal of human genetics, 1992-11, Vol.51 (5), p.964-970

1992

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Low-copy-number repeat sequences flank the DiGeorge/velo-cardio-facial syndrome loci at 22q11

Human molecular genetics, 1993-02, Vol.2 (2), p.191-196

1993

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DiGeorge syndrome with isolated aortic coarctation and isolated ventricular septal defect in three sibs with a 22q11 deletion of maternal origin

British Heart Journal, 1991-10, Vol.66 (4), p.308-312

1991

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Localization of 27 DNA markers to the region of human chromosome 22q11-pter deleted in patients with the DiGeorge syndrome and duplicated in the der22 syndrome

Genomics (San Diego, Calif.), 1990-07, Vol.7 (3), p.299-306

1990

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Defining the expressed breast cancer kinome

Cell research, 2012-04, Vol.22 (4), p.620-623

2012

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Inflammatory bowel disease: progress toward a gene

Canadian journal of gastroenterology, 2000-03, Vol.14 (3), p.207

2000

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Inflammatory bowel disease susceptibility loci defined by genome scan meta-analysis of 1952 affected relative pairs

Human molecular genetics, 2004-04, Vol.13 (7), p.763-770

2004

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Use of Commercially Available Radiation Hybrid Panels

Current Protocols in Human Genetics, 2001-05, Vol.25 (1), p.3.5.1-3.5.10

2001

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Inflammatory bowel disease is associated with a TNF polymorphism that affects an interaction between the OCT1 and NF-κB transcription factors

Human molecular genetics, 2002-05, Vol.11 (11), p.1281-1289

2002

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Association of the TSHR gene with Graves' disease: the first disease specific locus

European journal of human genetics : EJHG, 2005-11, Vol.13 (11), p.1223-1230

2005

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Chromosome dissection and cloning

Methods in molecular biology (Clifton, N.J.), 1994, Vol.29, p.425

1994

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Evidence for a Single Gene Effect Causing Polycystic Ovaries and Male Pattern Baldness

Obstetrical & gynecological survey, 1993-11, Vol.48 (11), p.753-755

1993

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The IBD6 Crohn's disease locus demonstrates complex interactions with CARD15 and IBD5 disease-associated variants

Human molecular genetics, 2003-10, Vol.12 (20), p.2569-2575

2003

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Interstitial deletions in DiGeorge syndrome detected with microclones from 22q11

Mammalian genome, 1992-01, Vol.3 (2), p.101-105

1992

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Identification of novel polymorphisms in the beta7 integrin gene: family-based association studies in inflammatory bowel disease

Genes and immunity, 2001-12, Vol.2 (8), p.455-460

2001

Volltextzugriff (PDF)

Identification of novel polymorphisms in the [beta]7 integrin gene: family-based association studies in inflammatory bowel disease

Genes and immunity, 2001-12, Vol.2 (8), p.455

2001

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The Ancient Source of a Distinct Gene Family Encoding Proteins Featuring RING and C3H Zinc-Finger Motifs with Abundant Expression in Developing Brain and Nervous System

Genomics (San Diego, Calif.), 2000-05, Vol.66 (1), p.76-86

2000

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