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B B de Vries

Showing results (1-10 of 27) with videos related to

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Journal of Medical Genetics|October 1, 1994
The Prader-Willi-like phenotype in fragile X patients: a designation facilitating clinical (and molecular) differential diagnosisB B De Vries, M F Niermeijer
Archives of Disease in Childhood|January 6, 1999
Skeletal dysplasiasC G Brook, B B de Vries
Journal of Medical Genetics|July 25, 1998
The fragile X syndromeB B de Vries, D J Halley, B A Oostra, et al.
Clinical Dysmorphology|April 20, 2001
Diagnostic dilemmas in four infants with nephrotic syndrome, microcephaly and severe developmental delayB B de Vries, W G van'tHoff, R A Surtees, et al.
Journal of Medical Genetics|May 19, 2001
Submicroscopic subtelomeric 1qter deletions: a recognisable phenotype?B B De Vries, S J Knight, T Homfray, et al.
Journal of Medical Genetics|March 2, 1999
Dilemmas in counselling females with the fragile X syndromeB B de Vries, H M van den Boer-van den Berg, M F Niermeijer, et al.
American Journal of Human Genetics|January 13, 2000
Benign hereditary chorea of early onset maps to chromosome 14qB B de Vries, W F Arts, G J Breedveld, et al.
American Journal of Medical Genetics|March 17, 2001
Submicroscopic 8pter deletion, mild mental retardation, and behavioral problems caused by a familial t(8;20)(p23;p13)B B de Vries, M Lees, S J Knight, et al.
Journal of Medical Genetics|December 10, 1997
DNA testing for fragile X syndrome: implications for parents and familyM A van Rijn, B B de Vries, A Tibben, et al.
Clinical Genetics|January 10, 2001
A boy with a submicroscopic 22qter deletion, general overgrowth and features suggestive of FG syndromeB B de Vries, M Bitner-Glindzicz, S J Knight, et al.
Pageof 3

Showing results (1-10 of 27) with videos related to

Sort By:
Pageof 3
Journal of Medical Genetics|October 1, 1994
The Prader-Willi-like phenotype in fragile X patients: a designation facilitating clinical (and molecular) differential diagnosisB B De Vries, M F Niermeijer
Archives of Disease in Childhood|January 6, 1999
Skeletal dysplasiasC G Brook, B B de Vries
Journal of Medical Genetics|July 25, 1998
The fragile X syndromeB B de Vries, D J Halley, B A Oostra, et al.
Clinical Dysmorphology|April 20, 2001
Diagnostic dilemmas in four infants with nephrotic syndrome, microcephaly and severe developmental delayB B de Vries, W G van'tHoff, R A Surtees, et al.
Journal of Medical Genetics|May 19, 2001
Submicroscopic subtelomeric 1qter deletions: a recognisable phenotype?B B De Vries, S J Knight, T Homfray, et al.
Journal of Medical Genetics|March 2, 1999
Dilemmas in counselling females with the fragile X syndromeB B de Vries, H M van den Boer-van den Berg, M F Niermeijer, et al.
American Journal of Human Genetics|January 13, 2000
Benign hereditary chorea of early onset maps to chromosome 14qB B de Vries, W F Arts, G J Breedveld, et al.
American Journal of Medical Genetics|March 17, 2001
Submicroscopic 8pter deletion, mild mental retardation, and behavioral problems caused by a familial t(8;20)(p23;p13)B B de Vries, M Lees, S J Knight, et al.
Journal of Medical Genetics|December 10, 1997
DNA testing for fragile X syndrome: implications for parents and familyM A van Rijn, B B de Vries, A Tibben, et al.
Clinical Genetics|January 10, 2001
A boy with a submicroscopic 22qter deletion, general overgrowth and features suggestive of FG syndromeB B de Vries, M Bitner-Glindzicz, S J Knight, et al.
Pageof 3