Parental Origin of the Extra Chromosome in Trisomy 21 as Indicated by Analysis of DNA Polymorphisms von Antonarakis, Stylianos E

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A dominantly inherited cytogenetic anomaly: a possible cell division mutant von RUDD, N. L, TESHIMA, I. E, MARTIN, R. H, SISKEN, J. E, WEKSBERG, R

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The meiotic stage of nondisjunction in trisomy 21 : determination by using DNA polymorphisms von ANTONARAKIS, S. E, PETERSEN, M. B, COHEN, M. M, ROULSON, D, SCHWARTZ, S, MIKKELSEN, M, TRANEBJAERG, L, GREENBERG, F, HOAR, D. I, RUDD, N. L, WARREN, A. C, METAXOTOU, C, MCINNIS, M. G, BARTSOCAS, C, CHAKRAVARTI, A, ADELSBERGER, P. A, SCHINZEL, A. A, BINKERT, F, PANGALOS, C, RAOUL, O, SLAUGENHAUPT, S. A, HAFEZ, M

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Ultrasound and Amniotic Fluid Alpha-Fetoprotein in the Prenatal Diagnosis of Spina Bifida von ALLEN, LYNN C, DORAN, TERENCE A, MISKIN, MURRAY, RUDD, NOREEN L, BENZIE, RONALD J, SHEFFIELD, LESLIE J

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PREGNANCY COMPLICATIONS IN TYPE IV EHLERS-DANLOS SYNDROME von Rudd, NoreenL, Holbrook, KarenA, Nimrod, Carl, Byers, PeterH

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Craniosynostosis. II. Coronal synostosis: Its familial characteristics and associated clinical findings in 109 patients lacking bilateral polysyndactyly or syndactyly von Hunter, Alasdair G. W., Rudd, Noreen L.

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The use of DNA probes to establish parental origin in Down syndrome von RUDD, N. L, DIMNIK, L. S, GREENTREE, C, MENDES-CRABB, K, HOAR, D. I

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A possible primidone embryopathy von Rudd, Noreen L., Freedom, Robert M.

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Micronucleus assay in human fibroblasts: A measure of spontaneous chromosomal instability and mutagen hypersensitivity von Rudd, Noreen L., Hoar, David I., Greentree, Carol L., Dimnik, Leo S., Hennig, Ursula G. G.

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The meiotic stage of nondisjunction in trisomy 21: determination by using DNA polymorphisms von Antonarakis, Stylianos E, Petersen, Michael B, McInnis, Melvin G, Adelsberger, Patricia A, Schinzel, Albert A, Binkert, Franz, Pangalos, Constantine, Raoul, Odile, Slaugenhaupt, Susan A, Hafez, Mohamed, Cohen, Maimon M, Roulson, Diane, Hoar, David I, Rudd, Noreen L, Warren, Andrew C, Metaxotou, Caterina, Bartsocas, Christos, Chakravarti, Aravinda

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Infant outcome following mid‐trimester amniocentesis: development and physical status at age six months von FINEGAN, JO‐ANNE K., QUARRINGTON, BRUCE J., HUGHES, HELEN E., RUDD, NOREEN L., STEVENS, LINDA J., WEKSBERG, ROSANNA, DORAN, TERENCE A.

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PRENATAL DIAGNOSIS OF HYPOPHOSPHATASIA von Hoar, DavidI, Rudd, NoreenL

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Thymic-renal-anal-lung dysplasia in sibs: A new autosomal recessive error of early morphogenesis von Rudd, Noreen L., Curry, Cynthia, Chen, Karl T. K., Capusten, Bernice, Trevenen, Cynthia L.

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Midtrimester amniocentesis: Obstetric outcome and neonatal neurobehavioral status von Finegan, Jo-Anne K., Quarrington, Bruce J., Hughes, Helen E., Rudd, Noreen L., Stevens, Linda J., Weksberg, Rosanna, Doran, Terence A.

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Maxillonasal dysplasia (Binder's syndrome) von Munro, I R, Sinclair, W J, Rudd, N L

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Arthrogryposis multiplex congenita-prenatal assessment with diagnostic ultrasound and fetoscopy von Miskin, Murray, Rothberg, Randy, Rudd, Noreen L., Benzie, Ronald J., Shime, Jerry

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PRENATAL DIAGNOSIS OF HYPOPHOSPHATASIA von Blau, Karl, Hoar, DavidI, Rattenbury, J.M, Rudd, NoreenL

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Craniosynostosis. I. Sagittal synostosis; Its genetics and associated clinical findings in 214 patients who lacked involvement of the coronal suture(s) von Hunter, Alasdair G. W., Rudd, Noreen L.

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A case of ring (9)/del(9p) mosaicism associated with gastroesophageal reflux von Leung, Alexander K. C., Rudd, Noreen L., Optiz, John M., Reynolds, James F.

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Prenatal diagnosis by fetoscopy with subsequent normal delivery: Report of a case von Benzie, Ronald J., Malone, Ralph M., Miskin, Murray, Rudd, Noreen L., Schofield, Philip A.

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