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T Lukusa

Showing results (11-20 of 33) with videos related to

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Clinical Dysmorphology|May 18, 1999
Mild dysmorphic signs in two male sibs with partial trisomy 2q32.1-->q35 due to maternal ins(14;2) translocationT Lukusa, K Devriendt, J Jaeken, et al.
Clinical Genetics|April 1, 1986
Gonadoblastoma and Y-chromosome fluorescenceT Lukusa, J P Fryns, H van den Berghe
Genetic Counseling (Geneva, Switzerland)|January 1, 1992
The role of the Y-chromosome in sex determinationT Lukusa, J P Fryns, H van der Berghe
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.
Genetic Counseling (Geneva, Switzerland)|May 23, 2002
Pericentric inversion with partial 7(q35-->qter) duplication and 7pter deletion: diagnosis by cytogenetic and fish analysis in a 29-year-old male patientT Lukusa, G Van Buggenhout, K Devriendt, et al.
Genetic Counseling (Geneva, Switzerland)|February 1, 2003
Small terminal 10q26 deletion in a male patient with Noonan-like stigmata: diagnosis by cytogenetic and FISH analysisT Lukusa, E Smeets, J R Vermeesch, et al.
Journal De Genetique Humaine|May 1, 1987
[Sexual ambiguity and a non-fluorescent Y chromosome]J P Fryns, T Lukusa, R Vereecken, et al.
Archives Francaises De Pediatrie|April 1, 1986
[Sexual ambiguity and non-fluorescent Y chromosome in 45,X/46,XY mosaicism]T Lukusa, J P Fryns, R Vereecken, et al.
Annales De Genetique|February 16, 2000
Proximal trisomy 13q and distal monosomy 8p in a dysmorphic and mentally retarded patient with an isodicentric chromosome 13q and a 13q/8p translocation chromosomeT Lukusa, L van den Berghe, E Smeets, et al.
Pageof 4

Showing results (11-20 of 33) with videos related to

Sort By:
Pageof 4
Clinical Dysmorphology|May 18, 1999
Mild dysmorphic signs in two male sibs with partial trisomy 2q32.1-->q35 due to maternal ins(14;2) translocationT Lukusa, K Devriendt, J Jaeken, et al.
Clinical Genetics|April 1, 1986
Gonadoblastoma and Y-chromosome fluorescenceT Lukusa, J P Fryns, H van den Berghe
Genetic Counseling (Geneva, Switzerland)|January 1, 1992
The role of the Y-chromosome in sex determinationT Lukusa, J P Fryns, H van der Berghe
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.
Genetic Counseling (Geneva, Switzerland)|May 23, 2002
Pericentric inversion with partial 7(q35-->qter) duplication and 7pter deletion: diagnosis by cytogenetic and fish analysis in a 29-year-old male patientT Lukusa, G Van Buggenhout, K Devriendt, et al.
Genetic Counseling (Geneva, Switzerland)|February 1, 2003
Small terminal 10q26 deletion in a male patient with Noonan-like stigmata: diagnosis by cytogenetic and FISH analysisT Lukusa, E Smeets, J R Vermeesch, et al.
Journal De Genetique Humaine|May 1, 1987
[Sexual ambiguity and a non-fluorescent Y chromosome]J P Fryns, T Lukusa, R Vereecken, et al.
Archives Francaises De Pediatrie|April 1, 1986
[Sexual ambiguity and non-fluorescent Y chromosome in 45,X/46,XY mosaicism]T Lukusa, J P Fryns, R Vereecken, et al.
Annales De Genetique|February 16, 2000
Proximal trisomy 13q and distal monosomy 8p in a dysmorphic and mentally retarded patient with an isodicentric chromosome 13q and a 13q/8p translocation chromosomeT Lukusa, L van den Berghe, E Smeets, et al.
Pageof 4