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A P Smits

Showing results (1-10 of 26) with videos related to

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American Journal of Medical Genetics|April 20, 1999
Menstrual disorders and endocrine profiles in fragile X carriers prior to 40 years of age: a pilot studyD D Braat, A P Smits, C M Thomas
Cancer|January 15, 1980
A case of AMMoL with 8/21 translocation and loss of the Y as probably secondary eventsT W Hustinx, J T Burghouts, J M Scheres, et al.
American Journal of Medical Genetics|April 1, 1992
Penetrance estimate of the fra(X) gene using Pointer versus direct estimateA F de Haan, A P Smits, D F Smeets, et al.
Human Reproduction (Oxford, England)|March 3, 2001
Increased serum FSH in female fragile X premutation carriers with either regular menstrual cycles or on oral contraceptivesR D Hundscheid, D D Braat, L A Kiemeney, et al.
Human Molecular Genetics|January 1, 1995
Hotspot for deletions in the CGG repeat region of FMR1 in fragile X patientsE de Graaff, P Rouillard, P J Willems, et al.
British Journal of Haematology|September 1, 1977
Monosomy 7 in two patients with a myeloproliferative disorderG Boetius, T W Hustinx, A P Smits, et al.
American Journal of Medical Genetics|April 1, 1992
Validation of linkage-based DNA-diagnosis of fragile X gene carriers with the CGG repeat probeB A van Oost, A P Smits, J C Dreesen, et al.
Human Reproduction (Oxford, England)|October 21, 1999
Familial idiopathic premature ovarian failure: an overrated and underestimated genetic disease?Y M van Kasteren, R D Hundscheid, A P Smits, et al.
American Journal of Medical Genetics|April 20, 1999
Psychometric assessment of families with X-linked mental retardationT van Roosmalen, A P Smits, G H Thoonen, et al.
American Journal of Medical Genetics|July 12, 1996
Familial X-linked mental retardation and isolated growth hormone deficiency: clinical and molecular findingsB C Hamel, A P Smits, B J Otten, et al.
Pageof 3

Showing results (1-10 of 26) with videos related to

Sort By:
Pageof 3
American Journal of Medical Genetics|April 20, 1999
Menstrual disorders and endocrine profiles in fragile X carriers prior to 40 years of age: a pilot studyD D Braat, A P Smits, C M Thomas
Cancer|January 15, 1980
A case of AMMoL with 8/21 translocation and loss of the Y as probably secondary eventsT W Hustinx, J T Burghouts, J M Scheres, et al.
American Journal of Medical Genetics|April 1, 1992
Penetrance estimate of the fra(X) gene using Pointer versus direct estimateA F de Haan, A P Smits, D F Smeets, et al.
Human Reproduction (Oxford, England)|March 3, 2001
Increased serum FSH in female fragile X premutation carriers with either regular menstrual cycles or on oral contraceptivesR D Hundscheid, D D Braat, L A Kiemeney, et al.
Human Molecular Genetics|January 1, 1995
Hotspot for deletions in the CGG repeat region of FMR1 in fragile X patientsE de Graaff, P Rouillard, P J Willems, et al.
British Journal of Haematology|September 1, 1977
Monosomy 7 in two patients with a myeloproliferative disorderG Boetius, T W Hustinx, A P Smits, et al.
American Journal of Medical Genetics|April 1, 1992
Validation of linkage-based DNA-diagnosis of fragile X gene carriers with the CGG repeat probeB A van Oost, A P Smits, J C Dreesen, et al.
Human Reproduction (Oxford, England)|October 21, 1999
Familial idiopathic premature ovarian failure: an overrated and underestimated genetic disease?Y M van Kasteren, R D Hundscheid, A P Smits, et al.
American Journal of Medical Genetics|April 20, 1999
Psychometric assessment of families with X-linked mental retardationT van Roosmalen, A P Smits, G H Thoonen, et al.
American Journal of Medical Genetics|July 12, 1996
Familial X-linked mental retardation and isolated growth hormone deficiency: clinical and molecular findingsB C Hamel, A P Smits, B J Otten, et al.
Pageof 3