D F Smeets|J M Scheres|T W Hustinx - JoVE Visualize

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Clinical Genetics|October 1, 1983

Congenital adrenal hypoplasia, progressive muscular dystrophy, and severe mental retardation, in association with glycerol kinase deficiency, in male sibsW O Renier, F A Nabben, T W Hustinx, et al.

Acta Neuropathologica|January 1, 1981

Connatal Pelizaeus-Merzbacher disease with congenital stridor in two maternal cousinsW O Renier, F J Gabreëls, T W Hustinx, et al.

Journal of Medical Genetics|October 1, 1992

Partial trisomy for 5q and monosomy for 12p in a liveborn child as a result of a complex five breakpoint chromosome rearrangement in a parentC J Van Der Burgt, G F Merkx, A H Janssen, et al.

American Journal of Medical Genetics|April 1, 1992

Penetrance of fra(X) gene: influence of grandparental origin of the gene, mental status of the carrier mother, and presence of a normal transmitting maleA P Smits, B A van Oost, A F de Haan, et al.

Journal of the American Academy of Dermatology|May 1, 1994

Congenital atrichia, palmoplantar hyperkeratosis, mental retardation, and early loss of teeth in four siblings: a new syndrome?P M Steijlen, H A Neumann, D J der Kinderen, et al.

Prenatal Diagnosis|April 1, 1997

Misinterpretation of trisomy 18 as a pseudomosaicism at third-trimester amniocentesis of a child with a mosaic 46,XY/47,XY, +3/48,XXY, +18 karyotypeC M van Ravenswaaij-Arts, J H Tuerlings, A F Van Heyst, et al.

Annales De Genetique|March 1, 1975

Trisomy 4p in a family with A t(4;15)W J Hustinx, J M Gabreëls, V G Kirkels, et al.

Cytogenetics and Cell Genetics|July 15, 2000

DNA hypomethylation and unusual chromosome instability in cell lines from ICF syndrome patientsC M Tuck-Muller, A Narayan, F Tsien, et al.

Cytogenetic and Genome Research|September 22, 2011

SNP array analysis in constitutional and cancer genome diagnostics--copy number variants, genotyping and quality controlN de Leeuw, J Y Hehir-Kwa, A Simons, et al.

International Journal of Cancer|July 15, 1988

Characterization of a human ovarian carcinoma cell line, OTN 14, derived from a mucinous cystadenocarcinomaC C van Niekerk, L G Poels, P H Jap, et al.

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Showing results (61-70 of 92) with videos related to

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Pageof 10

Clinical Genetics|October 1, 1983

Congenital adrenal hypoplasia, progressive muscular dystrophy, and severe mental retardation, in association with glycerol kinase deficiency, in male sibsW O Renier, F A Nabben, T W Hustinx, et al.

Acta Neuropathologica|January 1, 1981

Connatal Pelizaeus-Merzbacher disease with congenital stridor in two maternal cousinsW O Renier, F J Gabreëls, T W Hustinx, et al.

Journal of Medical Genetics|October 1, 1992

Partial trisomy for 5q and monosomy for 12p in a liveborn child as a result of a complex five breakpoint chromosome rearrangement in a parentC J Van Der Burgt, G F Merkx, A H Janssen, et al.

American Journal of Medical Genetics|April 1, 1992

Penetrance of fra(X) gene: influence of grandparental origin of the gene, mental status of the carrier mother, and presence of a normal transmitting maleA P Smits, B A van Oost, A F de Haan, et al.

Journal of the American Academy of Dermatology|May 1, 1994

Congenital atrichia, palmoplantar hyperkeratosis, mental retardation, and early loss of teeth in four siblings: a new syndrome?P M Steijlen, H A Neumann, D J der Kinderen, et al.

Prenatal Diagnosis|April 1, 1997

Misinterpretation of trisomy 18 as a pseudomosaicism at third-trimester amniocentesis of a child with a mosaic 46,XY/47,XY, +3/48,XXY, +18 karyotypeC M van Ravenswaaij-Arts, J H Tuerlings, A F Van Heyst, et al.

Annales De Genetique|March 1, 1975

Trisomy 4p in a family with A t(4;15)W J Hustinx, J M Gabreëls, V G Kirkels, et al.

Cytogenetics and Cell Genetics|July 15, 2000

DNA hypomethylation and unusual chromosome instability in cell lines from ICF syndrome patientsC M Tuck-Muller, A Narayan, F Tsien, et al.

Cytogenetic and Genome Research|September 22, 2011

SNP array analysis in constitutional and cancer genome diagnostics--copy number variants, genotyping and quality controlN de Leeuw, J Y Hehir-Kwa, A Simons, et al.

International Journal of Cancer|July 15, 1988

Characterization of a human ovarian carcinoma cell line, OTN 14, derived from a mucinous cystadenocarcinomaC C van Niekerk, L G Poels, P H Jap, et al.

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