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In memoriam Jacques Frederic

Revue médicale de Liège, 1994-08, Vol.49 (8), p.425

Koulischer, L

1994

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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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Les techniques récentes de procréation médicalement assistée et le conseil génétique

Andrologie (Lille, France), 1998-09, Vol.8 (3), p.321-328

1998

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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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Intrasplenic ovarian grafts in the castrated rabbit

Annales d'endocrinologie, 1960-05, Vol.21, p.314

KOULISCHER, L

1960

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Phase contrast study of human chromosomes

Comptes rendus hebdomadaires des séances de l'Académie des sciences, 1963-04, Vol.256, p.3350-3351

KOULISCHER, L

1963

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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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Human cytogenetics is born in Liège 80 years ago (de Winiwarter, 1912)

Revue médicale de Liège, 1993-03, Vol.48 (3), p.129

1993

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Apropos of a case of 22-trisomy

Bulletin de l'Academie royale de medecine de Belgique, 1962, Vol.2, p.329

1962

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Action of estrogenic treatment of the prolactin content in the grafted hypophysis of the rat

Comptes rendus des seances de la Societe de biologie et de ses filiales, 1960, Vol.154, p.1515-1517

1960

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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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L'isolation des cellules fœtales en circulation dans le sang maternel: mise au point

Immuno analyse & biologie spécialisée, 1997-11, Vol.12 (5), p.252-255

1997

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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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Non-radioactive assay of AFP, hCG, and uE3 from dried blood specimens: A low-cost alternative for maternal screening for trisomy 21

Prenatal diagnosis, 1992-12, Vol.12 (12), p.1073-1074

1992

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Chromosome abnormalities: prenatal diagnosis

Revue médicale de Liège, 1972-06, Vol.27, p.Suppl 1:61

Koulischer, L

1972

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Cytogenetic studies on wild house mice from Belgium

Genetica, 1990-02, Vol.80 (2), p.93-100

1990

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Hypoglossia-hypodactyly syndrome with hydrocephalus: a clue to the aetiology?

Journal of medical genetics, 1991-07, Vol.28 (7), p.490-491

1991

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Coloration de la region centromerique par les techniques desbandes C et R chez dix especes de ruminants

Comptes rendus des seances de la Societe de biologie et de ses filiales, 1978, Vol.172 (4), p.797-800

Koulischer, L

1978

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Chromosomes and speciation in Bovoidea

Archiv fur Genetik, 1974, Vol.47 (2), p.127

Koulischer, L

1974

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Down's syndrome in Wallonia (South Belgium), 1971-1978: cytogenetics and incidence

Human genetics, 1980-01, Vol.54 (2), p.243-250

1980

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Genetics and disorders of the osseous system

Acta orthopaedica belgica, 1965-07, Vol.31 (4), p.627

Koulischer, L

1965

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Microcephaly, macrotia, unusual mimics and mental retardation syndrome: new syndrome or variant of De Lange type 2 syndrome

Genetic counseling, 1996, Vol.7 (4), p.277

1996

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Primordial osteodysplastic dwarfism type I in association with corneal clouding: evidence for autosomal recessive inheritance

Clinical genetics, 1990-11, Vol.38 (5), p.359-361

1990

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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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In memoriam Jacques Frederic

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

Les techniques récentes de procréation médicalement assistée et le conseil génétique

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

Intrasplenic ovarian grafts in the castrated rabbit

Phase contrast study of human chromosomes

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

Human cytogenetics is born in Liège 80 years ago (de Winiwarter, 1912)

Apropos of a case of 22-trisomy

Action of estrogenic treatment of the prolactin content in the grafted hypophysis of the rat

Cytogenetic study of bovine oocytes matured in vitro

L'isolation des cellules fœtales en circulation dans le sang maternel: mise au point

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

Non-radioactive assay of AFP, hCG, and uE3 from dried blood specimens: A low-cost alternative for maternal screening for trisomy 21

Chromosome abnormalities: prenatal diagnosis

Cytogenetic studies on wild house mice from Belgium

Hypoglossia-hypodactyly syndrome with hydrocephalus: a clue to the aetiology?

Coloration de la region centromerique par les techniques desbandes C et R chez dix especes de ruminants

Chromosomes and speciation in Bovoidea

Down's syndrome in Wallonia (South Belgium), 1971-1978: cytogenetics and incidence

Genetics and disorders of the osseous system

Microcephaly, macrotia, unusual mimics and mental retardation syndrome: new syndrome or variant of De Lange type 2 syndrome

Primordial osteodysplastic dwarfism type I in association with corneal clouding: evidence for autosomal recessive inheritance

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

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