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Genetic Analysis of Rwandan Patients With Cystic Fibrosis-Like Symptoms

Chest, 2009-05, Vol.135 (5), p.1233-1242

2009

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Genetic Analysis of Rwandan Patients With Cystic Fibrosis-Like Symptoms: Identification of Novel Cystic Fibrosis Transmembrane Conductance Regulator and Epithelial Sodium Channel Gene Variants

Chest, 2009-05, Vol.135 (5), p.1233-1242

2009

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Clinical overlap of Beckwith‐Wiedemann, Perlman and Simpson‐Golabi‐Behmel syndromes: a diagnostic pitfall

Clinical genetics, 1995-05, Vol.47 (5), p.257-262

1995

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Aneurysms of the abdominal aorta: familial and genetic aspects in three hundred thirteen pedigrees

Journal of vascular surgery, 1995-04, Vol.21 (4), p.646-655

1995

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Microcephaly, muscular build, rhizomelia, and cataracts: Description of a possible recessive syndrome and some comments on the use of electronic databases in syndromology

American journal of medical genetics, 1997-02, Vol.68 (4), p.455-460

1997

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Deletion of the 5′‐ABL region: a recurrent anomaly detected by fluorescence in situ hybridization in about 10% of Philadelphia‐positive chronic myeloid leukaemia patients

British journal of haematology, 2000-07, Vol.110 (1), p.214-216

2000

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Mutation analysis of the MEN1 gene in Belgian patients with multiple endocrine neoplasia type 1 and related diseases

Human mutation, 1999, Vol.13 (1), p.54-60

1999

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Major decrease in the incidence of trisomy21 at birth in south Belgium: mass impact of triple test?

European journal of human genetics : EJHG, 2001-01, Vol.9 (1), p.1-4

2001

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Genetic Aspects of Abdominal Aortic Aneurysm

Annals of the New York Academy of Sciences, 1996-11, Vol.800 (1), p.44-55

1996

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Major Decrease in the Incidence of Trisomy 21 at Birth in South Belgium: Mass Impact of Triple Test?

European journal of human genetics : EJHG, 2001, Vol.9 (1), p.1-4

2001

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A low rate of trisomy 21 in twin-pregnancies: a cytogenetics retrospective study of 278 cases

Genetic counseling, 2003, Vol.14 (4), p.395

2003

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Loss of the Y chromosome in bone marrow cells: results on 1907 consecutive cases of leukaemia and preleukaemia

Clinical and laboratory haematology, 1999-02, Vol.21 (1), p.17-20

1999

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Recurrence of neonatal haemochromatosis in half sibs born of unaffected mothers

Journal of medical genetics, 1996-06, Vol.33 (6), p.444-449

1996

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A prenatal trisomy 21 screening program using α-fetoprotein, human chorionic gonadotropin, and free estriol assays on maternal dried blood

American journal of obstetrics and gynecology, 1995, Vol.172 (1), p.167-174

1995

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Cytogenetic study of bovine oocytes matured in vitro

Theriogenology, 1995-08, Vol.44 (3), p.445-450

1995

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A new form of skeletal dysplasia with amelogenesis imperfecta and platyspondyly

Clinical genetics, 1996-01, Vol.49 (1), p.2-5

1996

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Free Topic Meeting: Meiotic Chromosomes in Man and other Mammals

Clinical genetics, 1975-11, Vol.8 (5), p.394-395

Koulischer, Lucien

1975

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Brachymorphism-onychodysplasia-dysphalangism syndrome

Journal of medical genetics, 1993-02, Vol.30 (2), p.158-161

1993

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Oro-facial-digital syndrome II

Clinical genetics, 1988-02, Vol.33 (2), p.141-142

1988

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Letters to the Editors

Clinical genetics, 1983-04, Vol.23 (4), p.336-337

1983

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Letters to the Editors

Clinical genetics, 1983-04, Vol.23 (4), p.336-337

1983

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Letters to the Editors

Clinical genetics, 1983-04, Vol.23 (4), p.336-337

1983

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Indoor radon, an extrapulmonary genetic risk?

The Lancet (British edition), 1994-09, Vol.344 (8924), p.750-751

1994

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Journal of Medical Genetics

Journal of medical genetics, 1993, p.158-61

1993

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CHROMOSOME BANDING

The Lancet (British edition), 1973-10, Vol.302 (7835), p.967-967

Koulischer, Lucien

1973

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Genetic Analysis of Rwandan Patients With Cystic Fibrosis-Like Symptoms

Genetic Analysis of Rwandan Patients With Cystic Fibrosis-Like Symptoms: Identification of Novel Cystic Fibrosis Transmembrane Conductance Regulator and Epithelial Sodium Channel Gene Variants

Clinical overlap of Beckwith‐Wiedemann, Perlman and Simpson‐Golabi‐Behmel syndromes: a diagnostic pitfall

Aneurysms of the abdominal aorta: familial and genetic aspects in three hundred thirteen pedigrees

Microcephaly, muscular build, rhizomelia, and cataracts: Description of a possible recessive syndrome and some comments on the use of electronic databases in syndromology

Deletion of the 5′‐ABL region: a recurrent anomaly detected by fluorescence in situ hybridization in about 10% of Philadelphia‐positive chronic myeloid leukaemia patients

Mutation analysis of the MEN1 gene in Belgian patients with multiple endocrine neoplasia type 1 and related diseases

Major decrease in the incidence of trisomy21 at birth in south Belgium: mass impact of triple test?

Genetic Aspects of Abdominal Aortic Aneurysm

Major Decrease in the Incidence of Trisomy 21 at Birth in South Belgium: Mass Impact of Triple Test?

A low rate of trisomy 21 in twin-pregnancies: a cytogenetics retrospective study of 278 cases

Loss of the Y chromosome in bone marrow cells: results on 1907 consecutive cases of leukaemia and preleukaemia

Recurrence of neonatal haemochromatosis in half sibs born of unaffected mothers

A prenatal trisomy 21 screening program using α-fetoprotein, human chorionic gonadotropin, and free estriol assays on maternal dried blood

Cytogenetic study of bovine oocytes matured in vitro

A new form of skeletal dysplasia with amelogenesis imperfecta and platyspondyly

Free Topic Meeting: Meiotic Chromosomes in Man and other Mammals

Brachymorphism-onychodysplasia-dysphalangism syndrome

Oro-facial-digital syndrome II

Letters to the Editors

Letters to the Editors

Letters to the Editors

Indoor radon, an extrapulmonary genetic risk?

Journal of Medical Genetics

CHROMOSOME BANDING

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