P Moerman|J P Fryns - JoVE Visualize

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Liver|April 1, 1989

In situ localization of melanotransferrin (melanoma-associated antigen P97) in human liver. A light- and electronmicroscopic immunohistochemical studyR Sciot, R de Vos, P van Eyken, et al.

Journal of Medical Genetics|May 1, 1997

Trisomy 15 rescue with jumping translocation of distal 15q in Prader-Willi syndromeK Devriendt, P Petit, G Matthijs, et al.

Clinical Genetics|June 11, 1999

Partial DiGeorge syndrome in two patients with a 10p rearrangementH Van Esch, P Groenen, S Daw, et al.

Cytogenetics and Cell Genetics|January 1, 1996

Isolation of cosmids corresponding to the chromosome breakpoints of a de novo autosomal translocation, t(6;19)(p21;q13.1), in a patient with multicystic renal dysplasiaP M Groenen, E Garcia, R Thoelen, et al.

Genetic Counseling (Geneva, Switzerland)|November 6, 2001

Holoprosencephaly: the Maastricht experienceU Moog, C E De Die-Smulders, C T Schrander-Stumpel, et al.

European Journal of Human Genetics : EJHG|April 21, 2001

Parental mosaicism of JAG1 mutations in families with Alagille syndromeJ Giannakudis, A Röpke, A Kujat, et al.

American Journal of Medical Genetics|July 1, 1990

Restrictive dermopathy with distinct morphological abnormalitiesM Van Hoestenberghe, E Legius, W Vandevoorde, et al.

American Journal of Medical Genetics|March 3, 1998

Central nervous system malformations and early end-stage renal disease in oro-facio-digital syndrome type I: a reviewS Odent, B Le Marec, A Toutain, et al.

European Journal of Obstetrics, Gynecology, and Reproductive Biology|October 1, 1983

Thrombosis of the right umbilical artery, presumably related to the shortness of the umbilical cord: an unusual cause of fetal distressH Devlieger, P Moerman, J Lauweryns, et al.

European Journal of Gynaecological Oncology|June 22, 1999

Malignant trophoblastic disease following a twin pregnancy consisting of a complete hydatiform mole and a normal fetus and placenta. A case reportS Vandeginste, I B Vergote, M Hanssens, et al.

Pageof 89

Showing results (771-780 of 883) with videos related to

Sort By:

Pageof 89

Liver|April 1, 1989

In situ localization of melanotransferrin (melanoma-associated antigen P97) in human liver. A light- and electronmicroscopic immunohistochemical studyR Sciot, R de Vos, P van Eyken, et al.

Journal of Medical Genetics|May 1, 1997

Trisomy 15 rescue with jumping translocation of distal 15q in Prader-Willi syndromeK Devriendt, P Petit, G Matthijs, et al.

Clinical Genetics|June 11, 1999

Partial DiGeorge syndrome in two patients with a 10p rearrangementH Van Esch, P Groenen, S Daw, et al.

Cytogenetics and Cell Genetics|January 1, 1996

Isolation of cosmids corresponding to the chromosome breakpoints of a de novo autosomal translocation, t(6;19)(p21;q13.1), in a patient with multicystic renal dysplasiaP M Groenen, E Garcia, R Thoelen, et al.

Genetic Counseling (Geneva, Switzerland)|November 6, 2001

Holoprosencephaly: the Maastricht experienceU Moog, C E De Die-Smulders, C T Schrander-Stumpel, et al.

European Journal of Human Genetics : EJHG|April 21, 2001

Parental mosaicism of JAG1 mutations in families with Alagille syndromeJ Giannakudis, A Röpke, A Kujat, et al.

American Journal of Medical Genetics|July 1, 1990

Restrictive dermopathy with distinct morphological abnormalitiesM Van Hoestenberghe, E Legius, W Vandevoorde, et al.

American Journal of Medical Genetics|March 3, 1998

Central nervous system malformations and early end-stage renal disease in oro-facio-digital syndrome type I: a reviewS Odent, B Le Marec, A Toutain, et al.

European Journal of Obstetrics, Gynecology, and Reproductive Biology|October 1, 1983

Thrombosis of the right umbilical artery, presumably related to the shortness of the umbilical cord: an unusual cause of fetal distressH Devlieger, P Moerman, J Lauweryns, et al.

European Journal of Gynaecological Oncology|June 22, 1999

Malignant trophoblastic disease following a twin pregnancy consisting of a complete hydatiform mole and a normal fetus and placenta. A case reportS Vandeginste, I B Vergote, M Hanssens, et al.

Pageof 89