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De Smet L

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Publication

Featured researches published by De Smet L.

Genetic Counseling | 2002

Classification for congenital anomalies of the hand: the IFSSH classification and the JSSH modification

De Smet L

Genetic Counseling | 1999

THE CONCURRENCE OF RING CONSTRICTIONS IN ADAMS-OLIVER SYNDROME : ADDITIONAL EVIDENCE FOR VASCULAR DISRUPTION AS COMMON PATHOGENETIC MECHANISM

Keymolen K; De Smet L; Bracke P; Fryns Jp

Genetic Counseling | 1996

Holt-Oram syndrome with associated postaxial and central polydactyly. Further evidence for genetic heterogeneity in the Holt-Oram syndrome.

Fryns Jp; Bonnet D; De Smet L

Genetic Counseling | 2004

Emery-Dreifuss muscular dystrophy

De Smet L

Genetic Counseling | 2002

Unilateral absence of the trapezius and pectoralis major muscle: a variant of Poland syndrome.

Debeer P; Brys P; De Smet L; Fryns Jp

Genetic Counseling | 2002

Fetal hydantoin syndrome with unilateral atypical cleft hand: additional evidence for vascular disruption

De Smet L; Debeer P

Genetic Counseling | 2002

Unilateral absent scaphoid in a patient with «Holt-Oram» syndrome

De Smet L

Genetic Counseling | 2001

Hypoglossia-hypodactyly syndrome: report of 2 patients.

De Smet L; Schollen W

Genetic Counseling | 1993

Holt-oram syndrome: postaxial and central polydactyly as variable manifestations in a four generations family

Moens P; De Smet L; Fabry G; Fryns Jp

Genetic Counseling | 2008

Unilateral radio-ulnar synostosis and idic-Y chromosome.

De Smet L; Fryns Jp

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Collaboration

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Fryns Jp

Katholieke Universiteit Leuven

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Koenraad Devriendt

Katholieke Universiteit Leuven

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Boyan Dimitrov

Katholieke Universiteit Leuven

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Irina Balikova

Katholieke Universiteit Leuven

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R. Sciot

The Catholic University of America

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