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M Holvoet

Showing results (1-10 of 22) with videos related to

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American Journal of Medical Genetics|June 22, 1999
Follow-up of an adult with Keutel syndromeK Devriendt, M Holvoet, J P Fryns
Genetic Counseling (Geneva, Switzerland)|October 20, 1998
Further delineation of the KBG syndromeK Devriendt, M Holvoet, J P Fryns
Clinical Genetics|October 27, 1998
Severe mental retardation-distal arthrogryposis in the upper limbs and complex chromosomal rearrangements resulting from a 10q25-->qter deletionT Lukusa, K Devriendt, M Holvoet, et al.
American Journal of Medical Genetics|April 11, 2000
Dicentric chromosome 9 due to tandem duplication of the 9p11-q13 region: unusual chromosome 9 variantT Lukusa, K Devriendt, M Holvoet, et al.
Clinical Genetics|March 25, 2000
The Haspeslagh syndrome (MIM 177980) is caused by an unbalanced reciprocal 6q/9p translocationK Devriendt, M Holvoet, A De Mûelenaere, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1996
Marden-Walker phenotype: a diagnostic dilemmaD Soekarman, P Volcke, E Legius, et al.
Journal of Medical Genetics|April 16, 1999
Triplication of distal chromosome 10qK Devriendt, G Matthijs, M Holvoet, et al.
Genetic Counseling (Geneva, Switzerland)|November 3, 2004
Deletion 2q37.3 and autism: molecular cytogenetic mapping of the candidate region for autistic disorderT Lukusa, J R Vermeesch, M Holvoet, et al.
Genetic Counseling (Geneva, Switzerland)|July 23, 2003
Partial monosomy 11q and trisomy 12q: variable expression in two siblingsT Lukusa, M Holvoet, J R Vermeesch, et al.
American Journal of Medical Genetics|October 28, 1997
A recognisable behavioural phenotype associated with terminal deletions of the short arm of chromosome 8I Claeys, M Holvoet, B Eyskens, et al.
Pageof 3

Showing results (1-10 of 22) with videos related to

Sort By:
Pageof 3
American Journal of Medical Genetics|June 22, 1999
Follow-up of an adult with Keutel syndromeK Devriendt, M Holvoet, J P Fryns
Genetic Counseling (Geneva, Switzerland)|October 20, 1998
Further delineation of the KBG syndromeK Devriendt, M Holvoet, J P Fryns
Clinical Genetics|October 27, 1998
Severe mental retardation-distal arthrogryposis in the upper limbs and complex chromosomal rearrangements resulting from a 10q25-->qter deletionT Lukusa, K Devriendt, M Holvoet, et al.
American Journal of Medical Genetics|April 11, 2000
Dicentric chromosome 9 due to tandem duplication of the 9p11-q13 region: unusual chromosome 9 variantT Lukusa, K Devriendt, M Holvoet, et al.
Clinical Genetics|March 25, 2000
The Haspeslagh syndrome (MIM 177980) is caused by an unbalanced reciprocal 6q/9p translocationK Devriendt, M Holvoet, A De Mûelenaere, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1996
Marden-Walker phenotype: a diagnostic dilemmaD Soekarman, P Volcke, E Legius, et al.
Journal of Medical Genetics|April 16, 1999
Triplication of distal chromosome 10qK Devriendt, G Matthijs, M Holvoet, et al.
Genetic Counseling (Geneva, Switzerland)|November 3, 2004
Deletion 2q37.3 and autism: molecular cytogenetic mapping of the candidate region for autistic disorderT Lukusa, J R Vermeesch, M Holvoet, et al.
Genetic Counseling (Geneva, Switzerland)|July 23, 2003
Partial monosomy 11q and trisomy 12q: variable expression in two siblingsT Lukusa, M Holvoet, J R Vermeesch, et al.
American Journal of Medical Genetics|October 28, 1997
A recognisable behavioural phenotype associated with terminal deletions of the short arm of chromosome 8I Claeys, M Holvoet, B Eyskens, et al.
Pageof 3