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Biochimica Et Biophysica Acta
|
December 15, 2007
Human chromosome fragility
T Lukusa, J P Fryns
Genetic Counseling (Geneva, Switzerland)
|
July 14, 2000
Pure distal monosomy 10q26 in a patient displaying clinical features of Prader-Willi syndrome during infancy and distinct behavioural phenotype in adolescence
T Lukusa, J P Fryns
American Journal of Medical Genetics
|
January 8, 1999
Syndrome of facial, oral, and digital anomalies due to 7q21.2-->q22.1 duplication
T Lukusa, J P Fryns
Biochimica Et Biophysica Acta
|
November 3, 2007
WITHDRAWN: Human chromosome fragility
T Lukusa, J P Fryns
Genetic Counseling (Geneva, Switzerland)
|
April 28, 2010
Pure de novo 17q25.3 micro duplication characterized by micro array CGH in a dysmorphic infant with growth retardation, developmental delay and distal arthrogryposis
T Lukusa, J P Fryns
Annales De Genetique
|
August 6, 1999
A 3p deletion syndrome in a child with both del(3)(p25-->pter) and dup(17)(q23-->qter)
T Lukusa, K Devriendt, J P Fryns
Accident; Analysis and Prevention
|
September 29, 2019
A Horvitz-type estimation on incomplete traffic accident data analyzed via a zero-inflated Poisson model
Martin T Lukusa, Frederick Kin Hing Phoa
Genetic Counseling (Geneva, Switzerland)
|
January 1, 1996
Caudal developmental field defect with female pseudohermaphroditism and VACTERL anomalies
T Lukusa, P Moerman, J P Fryns
Genetic Counseling (Geneva, Switzerland)
|
April 23, 2005
De novo deletion 7q36 resulting from a distal 7q/8q translocation: phenotypic expression and comparison to the literature
T Lukusa, J R Vermeesch, J P Fryns
European Journal of Pediatrics
|
December 1, 1986
Internal male pseudohermaphroditism in a 6 week old child
T Lukusa, J P Fryns, H Van den Berghe
Page
of 4
Search research articles
Search
Showing results (1-10 of 33) with videos related to
Sort By:
Page
of 4
Biochimica Et Biophysica Acta
|
December 15, 2007
Human chromosome fragility
T Lukusa, J P Fryns
Genetic Counseling (Geneva, Switzerland)
|
July 14, 2000
Pure distal monosomy 10q26 in a patient displaying clinical features of Prader-Willi syndrome during infancy and distinct behavioural phenotype in adolescence
T Lukusa, J P Fryns
American Journal of Medical Genetics
|
January 8, 1999
Syndrome of facial, oral, and digital anomalies due to 7q21.2-->q22.1 duplication
T Lukusa, J P Fryns
Biochimica Et Biophysica Acta
|
November 3, 2007
WITHDRAWN: Human chromosome fragility
T Lukusa, J P Fryns
Genetic Counseling (Geneva, Switzerland)
|
April 28, 2010
Pure de novo 17q25.3 micro duplication characterized by micro array CGH in a dysmorphic infant with growth retardation, developmental delay and distal arthrogryposis
T Lukusa, J P Fryns
Annales De Genetique
|
August 6, 1999
A 3p deletion syndrome in a child with both del(3)(p25-->pter) and dup(17)(q23-->qter)
T Lukusa, K Devriendt, J P Fryns
Accident; Analysis and Prevention
|
September 29, 2019
A Horvitz-type estimation on incomplete traffic accident data analyzed via a zero-inflated Poisson model
Martin T Lukusa, Frederick Kin Hing Phoa
Genetic Counseling (Geneva, Switzerland)
|
January 1, 1996
Caudal developmental field defect with female pseudohermaphroditism and VACTERL anomalies
T Lukusa, P Moerman, J P Fryns
Genetic Counseling (Geneva, Switzerland)
|
April 23, 2005
De novo deletion 7q36 resulting from a distal 7q/8q translocation: phenotypic expression and comparison to the literature
T Lukusa, J R Vermeesch, J P Fryns
European Journal of Pediatrics
|
December 1, 1986
Internal male pseudohermaphroditism in a 6 week old child
T Lukusa, J P Fryns, H Van den Berghe
Page
of 4