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M Verjaal

Showing results (11-20 of 29) with videos related to

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Clinical Genetics|December 1, 1984
Familial occurrence of azoospermia and extreme oligozoospermiaW J Budde, M Verjaal, J V Hamerlynck, et al.
Prenatal Diagnosis|June 1, 1987
Karyotypic differences between cells from placenta and other fetal tissuesM Verjaal, N J Leschot, H Wolf, et al.
Journal of the Neurological Sciences|December 1, 1988
Amyotrophy of the hands and pyramidal features of predominantly the legs segregating within one large familyM de Visser, B W Ongerboer de Visser, M Verjaal
Bone Marrow Transplantation|March 29, 2000
Prenatal HLA-matching to determine suitability for allogeneic bone marrow transplantationH van den Berg, M Verjaal, K Boer, et al.
Nederlands Tijdschrift Voor Geneeskunde|May 2, 1992
[Social support following induced abortion for genetic indications: experiences of the women concerned and their partners]N J Leschot, M Verjaal, P E Treffers, et al.
Clinical Genetics|March 1, 1990
Monosomy X found at first trimester CVS: a diagnostic and counselling dilemmaN J Leschot, H Wolf, M Verjaal, et al.
Human Genetics|June 30, 1977
Rapid prenatal diagnosis of HG-PRT deficiency using ultra-microchemical methodsP Hösli, C H de Bruyn, F J Oerlemans, et al.
Human Genetics|September 19, 1978
Prenatal diagnosis of Meckel syndromeN J Leschot, J J de Nef, M J Becker-Bloemkolk, et al.
Human Genetics|July 1, 1987
Human alpha-globin maps to pter-p13.3 in chromosome 16 distal to PGPM H Breuning, K Madan, M Verjaal, et al.
Lancet (London, England)|July 30, 1994
Prenatal diagnosis of type I hereditary tyrosinaemiaJ K Ploos van Amstel, R P Jansen, M Verjaal, et al.
Pageof 3

Showing results (11-20 of 29) with videos related to

Sort By:
Pageof 3
Clinical Genetics|December 1, 1984
Familial occurrence of azoospermia and extreme oligozoospermiaW J Budde, M Verjaal, J V Hamerlynck, et al.
Prenatal Diagnosis|June 1, 1987
Karyotypic differences between cells from placenta and other fetal tissuesM Verjaal, N J Leschot, H Wolf, et al.
Journal of the Neurological Sciences|December 1, 1988
Amyotrophy of the hands and pyramidal features of predominantly the legs segregating within one large familyM de Visser, B W Ongerboer de Visser, M Verjaal
Bone Marrow Transplantation|March 29, 2000
Prenatal HLA-matching to determine suitability for allogeneic bone marrow transplantationH van den Berg, M Verjaal, K Boer, et al.
Nederlands Tijdschrift Voor Geneeskunde|May 2, 1992
[Social support following induced abortion for genetic indications: experiences of the women concerned and their partners]N J Leschot, M Verjaal, P E Treffers, et al.
Clinical Genetics|March 1, 1990
Monosomy X found at first trimester CVS: a diagnostic and counselling dilemmaN J Leschot, H Wolf, M Verjaal, et al.
Human Genetics|June 30, 1977
Rapid prenatal diagnosis of HG-PRT deficiency using ultra-microchemical methodsP Hösli, C H de Bruyn, F J Oerlemans, et al.
Human Genetics|September 19, 1978
Prenatal diagnosis of Meckel syndromeN J Leschot, J J de Nef, M J Becker-Bloemkolk, et al.
Human Genetics|July 1, 1987
Human alpha-globin maps to pter-p13.3 in chromosome 16 distal to PGPM H Breuning, K Madan, M Verjaal, et al.
Lancet (London, England)|July 30, 1994
Prenatal diagnosis of type I hereditary tyrosinaemiaJ K Ploos van Amstel, R P Jansen, M Verjaal, et al.
Pageof 3