Molecular basis of choroideremia (CHM): Mutations involving the rab escort protein-1 (REP-1) gene von van den Hurk, JAJM, Schwartz, M, van Bokhoven, H, van de Pol, TJR, Bogerd, L, Pinckers, AJLG, Bleeker-Wagemakers, EM, Pawlowitzki, IH, Rüther, K, Ropers, H-H, Cremers, FPM

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Mutation spectrum in the CHM gene of Danish and Swedish choroideremia patients von Bokhoven, Hans van, Schwartz, Marianne, Andréasson, Sten, Hurk, José A. J. M. van den, Bogerd, Liesbeth, Jay, Marcelle, Rüther, Klaus, Jay, B., Pawlowitzki, Ivar H., Sankila, Eeva-Marja, Wright, Alan, Ropers, Hans-Hilger, Rosenberg, Thomas, Cremers, Frans P. M.

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Detection and characterization of point mutations in the choroideremia candidate gene by PCR-SSCP analysis and direct DNA sequencing von VAN DEN HURK, J. A. J. M, VAN DE POL, T. J. R, ROPERS, H.-H, CREMERS, F. P. M, MOLLOY, C. M, BRUNSMANN, F, RÜTHER, K, ZRENNER, E, PINCKERS, A. J. L. G, PAWLOWITZKI, I. H, BLEEKER-WAGEMAKERS, E. M, WIERINGA, B

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Trisomy 20 mosaicism von Miny, P., Pawlowitzki, I.-H.

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Inv dup (15): Prenatal diagnosis and postnatal follow-up von Miny, P., Basaran, S., Kuwertz, E., Holzgreve, W., Pawlowitzki, I.-H.

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False negative cytogenetic result in direct preparations after CVS von Miny, P., Basaran, S., Holzgreve, W., Horst, J., Pawlowitzki, I. H., Ngo, T. Kim Nhan

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Feto-maternal transfusion after chorionic villus sampling: evaluation by maternal serum alphafetoprotein measurement von FUHRMANN, W, ATLAND, K, KÖHLER, A, HOLZGREVE, W, JOVANOVIC, V, RAUSKOLB, R, PAWLOWITZKI, I. H, MINY, P

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C-band polymorphisms of chromosome 9: quantification by Ce-bands von WAHEDI, K, PAWLOWITZKI, I. H

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Choroideremia-locus maps between DXS3 and DXS11 on Xq von GAL, A, BRUNSMANN, F, HOGENKAMP, D, RÜTHER, K, AHLERT, D, WIENKER, T. F, HAMMERSTEIN, W, PAWLOWITZKI, I. H

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Elevated amniotic alpha fetoprotein in a fetus with Turner's syndrome due to puncture of a cystic hygroma von Pawlowitzki, I.H., Wörmann, B.

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Amniotic fluid acetylcholinesterase as a marker in prenatal diagnosis of esophageal atresia von Holzgreve, W., Beller, F.K., Pawlowitzki, I.H.

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A sex cord stromal tumour in a woman with XO/XX/XXX-mosaicism von Glaser, D, Nienhaus, H, Köhler, R, Walther, G, Pawlowitzki, I H

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Deletions in patients with classical choroideremia vary in size from 45 kb to several megabases von CREMERS, F. P. M, SANKILA, E.-M, DE LA CHAPELLE, A, PAWLOWITZKI, I. H, ROPERS, H.-H, BRUNSMANN, F, JAY, M, JAY, B, WRIGHT, A, PINCKERS, A. J. L. G, SCHWARTZ, M, VAN DE POL, D. J. R, WIERINGA, B

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The correspondence between quinacrine banding patterns and sites of secondary constrictions in human chromosomes von Pawlowitzki, I. H.

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Estimating frequency of Kallmann syndrome among hypogonadic and among anosmic patients von Pawlowitzki, I. Harry, Diekstall, Peter, Schadel, Alex, Miny, Peter, Reynolds, James F.

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Validity of cytogenetic analyses from trophoblast tissue throughout gestation von Miny, Peter, Basaran, Seher, Pawlowitzki, I. Harry, Horst, Jürgen, Westendorp, Andre, Niedner, Wolfram, Holzgreve, Wolfgang

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Rapid karyotyping for prenatal diagnosis in the second and third trimesters of pregnancy von Basaran, Seher, Miny, Peter, Pawlowitzki, Ivar-Harry, Horst, Jürgen, Holzgreve, Wolfgang

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Hae III restriction of DNA from three cases with nonfluorescent Y chromosomes (45XO/46XYnf) von GÄNSHIRT, D, PAWLOWITZKI, I. H

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Prenatal exclusion of choroideremia von van den Hurk, J. A. J. M., van Zandvoort, P. M., Brunsmann, F., Pawlowitzki, I. H., Holzgreve, W., Szabo, P., Cremers, F. P. M., van Oost, B. A.

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The effect of isoniazid (INH) on Chinese hamster and mouse spermatogonia von Miltenburger, H G, Träger, H, Adler, I D, Schmaltz, A, Rathenberg, R, Schwegler, H, Pawlowitzki, I H, Nautsch, C, Müller, D

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