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Oligodactyly and multiple synostoses of the extremities: two cases in sibs. A variant of Cenani-Lenz syndactyly

Human genetics, 1979-04, Vol.48 (2), p.183-189

Dodinval, P

1979

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PRENATAL DIAGNOSIS OF CYSTIC HYGROMA AND CHORIOANGIOMA IN THE WOLF-HIRSCHHORN SYNDROME

Prenatal diagnosis, 1991-02, Vol.11 (2), p.129-132

1991

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Rieger anomaly and uveal coloboma with associated anomalies:Third observation of a rare oculo-palato-osseous syndrome - the Abruzzo-Erikson syndrome

Ophthalmic genetics, 1990, Vol.11 (1), p.41-47

1990

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3C syndrome: third occurrence of cranio‐cerebello‐cardiac dysplasia (Ritscher‐Schinzel syndrome)

Clinical genetics, 1989-03, Vol.35 (3), p.205-208

1989

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Death through injection of barbiturates

Forensic science international, 1987-10, Vol.35 (2), p.141-144

1987

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Facial asymmetries: problems in genetic counselling

Journal de genetique humaine, 1979-10, Vol.27 (3), p.189

Dodinval, P

1979

Volltextzugriff (PDF)

The genetic prognosis in medicine

Revue médicale de Liège, 1961-07, Vol.16, p.410

DODINVAL, P

1961

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Distribution of the A, B, O and AB blood groups in Belgium

Bulletin de l'Academie royale de medecine de Belgique, 1961, Vol.1, p.171

DODINVAL, P

1961

Volltextzugriff (PDF)

Partial trisomy 20q due to paternal t(8;20) translocation: Case report and review of the literature

Clinical genetics, 1988-05, Vol.33 (5), p.386-389

1988

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A hydropic fetus with translucent ribs, arthrogryposis multiplex congenita and congenital myopathy: etiological heterogeneity of A.M.C., Toriello-Bauserman type?

Genetic counseling, 1991, Vol.2 (1), p.63

1991

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Distribution of matrimonial migrations in Belgium

Human heredity, 1973, Vol.23 (1), p.59

Dodinval, P A

1973

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Population structure of A,B,O,AB blood groups in Belgium

Human heredity, 1970, Vol.20 (2), p.169

Dodinval, P A

1970

Volltextzugriff (PDF)

Fetal Krabbe leukodystrophy. A morphologic study of two cases

Acta neuropathologica, 1981, Vol.53 (2), p.87-91

1981

Volltextzugriff (PDF)

The importance of genetic consultation for the general practitioner

Revue médicale de Liège, 1963-04, Vol.18, p.238

1963

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Identification of a skeleton and timing of death months later

Acta medicinae legalis et socialis, 1990, Vol.40, p.167

1990

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Genetic structure of Switzerland

American journal of human genetics, 1973-07, Vol.25 (4), p.347-361

1973

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DETECTION OF CARRIER STATE FOR PHENYLKETONURIA IN FAMILIAL GENETIC INVESTIGATIONS

Acta genetica et statistica medica, 1964, Vol.14, p.327

1964

Volltextzugriff (PDF)

Lambotte syndrome: Microcephaly, holoprosencephaly, intrauterine growth retardation, facial anomalies, and early lethality-A new sublethal multiple congenital anomaly/mental retardation syndrome in four sibs

American journal of medical genetics, 1990-09, Vol.37 (1), p.119-123

1990

Volltextzugriff (PDF)

Glaucoma-lens ectopia-microspherophakia-stiffness-shortness (GEMSS) syndrome: A dominant disease with manifestations of Weill-Marchesani syndromes

American journal of medical genetics, 1992-09, Vol.44 (1), p.48-51

1992

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Demographic characteristics and genetics in a small Savoy village (consanguinity, multiple hereditary diseases)

Journal de genetique humaine, 1962-03, Vol.11, p.1

1962

Volltextzugriff (PDF)

Does medical progress entail deterioration of our genetic heritage?

Revue médicale de Liège, 1980-01, Vol.35 (1), p.11

Dodinval, P

1980

Volltextzugriff (PDF)

Heredity in congenital dislocation of the hip

Acta orthopaedica belgica, 1990, Vol.56 (1 Pt A), p.7

Dodinval, P

1990

Volltextzugriff (PDF)

Genetic counselling in unexpected familial recurrence of achondroplasia

American journal of medical genetics, 1987-12, Vol.28 (4), p.949-954

1987

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A propos de la dysplasie des cr tes pidermiques: Mise en vidence d'une dysplasie apicale des doigts

Human genetics, 1972, Vol.15 (1), p.20-24

Dodinval, P.

1972

Volltextzugriff (PDF)

The mentally retarded. Viewpoint of a geneticist

Revue médicale de Liège, 1975-03, Vol.30 (5), p.164

Dodinval, P

1975

Volltextzugriff (PDF)

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Oligodactyly and multiple synostoses of the extremities: two cases in sibs. A variant of Cenani-Lenz syndactyly

PRENATAL DIAGNOSIS OF CYSTIC HYGROMA AND CHORIOANGIOMA IN THE WOLF-HIRSCHHORN SYNDROME

Rieger anomaly and uveal coloboma with associated anomalies:Third observation of a rare oculo-palato-osseous syndrome - the Abruzzo-Erikson syndrome

3C syndrome: third occurrence of cranio‐cerebello‐cardiac dysplasia (Ritscher‐Schinzel syndrome)

Death through injection of barbiturates

Facial asymmetries: problems in genetic counselling

The genetic prognosis in medicine

Distribution of the A, B, O and AB blood groups in Belgium

Partial trisomy 20q due to paternal t(8;20) translocation: Case report and review of the literature

A hydropic fetus with translucent ribs, arthrogryposis multiplex congenita and congenital myopathy: etiological heterogeneity of A.M.C., Toriello-Bauserman type?

Distribution of matrimonial migrations in Belgium

Population structure of A,B,O,AB blood groups in Belgium

Fetal Krabbe leukodystrophy. A morphologic study of two cases

The importance of genetic consultation for the general practitioner

Identification of a skeleton and timing of death months later

Genetic structure of Switzerland

DETECTION OF CARRIER STATE FOR PHENYLKETONURIA IN FAMILIAL GENETIC INVESTIGATIONS

Lambotte syndrome: Microcephaly, holoprosencephaly, intrauterine growth retardation, facial anomalies, and early lethality-A new sublethal multiple congenital anomaly/mental retardation syndrome in four sibs

Glaucoma-lens ectopia-microspherophakia-stiffness-shortness (GEMSS) syndrome: A dominant disease with manifestations of Weill-Marchesani syndromes

Demographic characteristics and genetics in a small Savoy village (consanguinity, multiple hereditary diseases)

Does medical progress entail deterioration of our genetic heritage?

Heredity in congenital dislocation of the hip

Genetic counselling in unexpected familial recurrence of achondroplasia

A propos de la dysplasie des cr tes pidermiques: Mise en vidence d'une dysplasie apicale des doigts

The mentally retarded. Viewpoint of a geneticist

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