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F Smeets

Showing results (61-70 of 104) with videos related to

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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.
The Journal of Physical Chemistry Letters|December 22, 2017
Anomalous Dependence of the Reactivity on the Presence of Steps: Dissociation of D<sub>2</sub> on Cu(211)Gernot Füchsel, Kun Cao, Süleyman Er, 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.
European Journal of Immunology|January 1, 1993
Phosphorylation of surface E-selectin and the effect of soluble ligand (sialyl Lewisx) on the half-life of E-selectinE F Smeets, T de Vries, J F Leeuwenberg, 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.
FEBS Letters|January 31, 2025
Characteristics of the Kelch domain containing (KLHDC) subfamily and relationships with diseasesCourtney Pilcher, Paula Armina V Buco, Jia Q Truong, 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.
The Journal of Investigative Dermatology|April 1, 1992
In situ detection of supernumerary aberrations of chromosome-specific repetitive DNA targets in interphase nuclei in human melanoma cell lines and tissue sectionsP E de Wit, A H Hopman, G N van Muijen, et al.
Clinical Dysmorphology|September 6, 2007
Tall stature and minor facial dysmorphisms in a patient with a 17.5 Mb interstitial deletion of chromosome 13 (q14.3q21.33): clinical report and reviewBregje W M van Bon, David A Koolen, Ilse Feenstra, et al.
Pageof 11

Showing results (61-70 of 104) with videos related to

Sort By:
Pageof 11
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.
The Journal of Physical Chemistry Letters|December 22, 2017
Anomalous Dependence of the Reactivity on the Presence of Steps: Dissociation of D<sub>2</sub> on Cu(211)Gernot Füchsel, Kun Cao, Süleyman Er, 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.
European Journal of Immunology|January 1, 1993
Phosphorylation of surface E-selectin and the effect of soluble ligand (sialyl Lewisx) on the half-life of E-selectinE F Smeets, T de Vries, J F Leeuwenberg, 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.
FEBS Letters|January 31, 2025
Characteristics of the Kelch domain containing (KLHDC) subfamily and relationships with diseasesCourtney Pilcher, Paula Armina V Buco, Jia Q Truong, 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.
The Journal of Investigative Dermatology|April 1, 1992
In situ detection of supernumerary aberrations of chromosome-specific repetitive DNA targets in interphase nuclei in human melanoma cell lines and tissue sectionsP E de Wit, A H Hopman, G N van Muijen, et al.
Clinical Dysmorphology|September 6, 2007
Tall stature and minor facial dysmorphisms in a patient with a 17.5 Mb interstitial deletion of chromosome 13 (q14.3q21.33): clinical report and reviewBregje W M van Bon, David A Koolen, Ilse Feenstra, et al.
Pageof 11