J. Knops

发表

Androgenetic/biparental mosaicism causes placental mesenchymal dysplasia

C. Livasy, L. Lefebvre, W. Robinson, 2005, Journal of Medical Genetics.

Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15 in a boy with a balanced 3;21 translocation.

A. Carroll, V. Proud, R. Michaelis, 2001, American journal of medical genetics.

Prospective study of 22q11 deletion analysis in fetuses with excess nuchal translucency.

A. Donnenfeld, D. Cutillo, J. Knops, 2006, American journal of obstetrics and gynecology.

Localization of human elav-like neuronal protein 1 (Hel-N1) on chromosome 9p21 by chromosome microdissection polymerase chain reaction and fluorescence in situ hybridization.

J. Longshore, P. King, J. Han, 1996, Genomics.

In situ analysis of the transcriptional activity of integrated viral DNA using tyramide-FISH.

B. V. Van Tine, L. Chow, J. Knops, 2001, Developments in biologicals.

Clonal Selection for Transcriptionally Active Viral Oncogenes during Progression to Cancer

J. Kappes, C. Meijer, P. Snijders, 2004, Journal of Virology.

Assignment1 of human MFNG, manic fringe Drosophila homolog, to 22q13.1 using tyramide fluorescence in situ hybridization (T-FISH)

G. Shaw, W. May, B. V. Van Tine, 1999, Cytogenetic and Genome Research.

Localization of HuC (ELAVL3) to chromosome 19p13.2 by fluorescence in situ hybridization utilizing a novel tyramide labeling technique.

A. Butler, P. Deloukas, G. Shaw, 1998, Genomics.

Chromosome abnormalities identified in 347 spontaneous abortions collected in Japan

Tatsuo Yamamoto, M. Nagaishi, K. Iinuma, 2004, The journal of obstetrics and gynaecology research.

Increased frequency of lymphocytic mitotic non-disjunction in recurrent spontaneous aborters.

R. C. Juberg, J. Knops, P. Mowrey, 1985, Journal of medical genetics.

Intra- and Intermolecular Triplex DNA Formation in the Murine c-myb Proto-Oncogene Promoter Are Inhibited by Mithramycin

V. Potaman, J. Trent, Donald M Miller, 2001, Biological chemistry.

Molecular and cytogenetic investigation of complex tissue-specific duplication and loss of chromosome 21 in a child with a monosomy 21 phenotype.

T. Hassold, N. Takaesu, P. Scarbrough, 1992, American journal of medical genetics.

Standardization of a PPD preparation in guinea-pigs and in man.

M. Uydebrouck, R. Dobbelaer, E. Meulepas, 1977, Journal of biological standardization.

Assignment of a Human Voltage-Dependent Sodium Channel α-Subunit Gene (SCN6A) to 2q21-q23

A. George, M. Tamkun, G. B. Brown, 1994 .

Assignment of the human heart tetrodotoxin-resistant voltage-gated Na+ channel alpha-subunit gene (SCN5A) to band 3p21.

D C Ward, D. Ward, H. Drabkin, 1995, Cytogenetics and cell genetics.