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Table of contents of journal: *American journal of medical genetics

Results: 1-25/992

Authors: Pelias, MK
Citation: Mk. Pelias, Emmanuel Shapira, MD, PhD 1933-1998 - In memoriam, AM J MED G, 80(5), 1998, pp. 441-442

Authors: Meschede, D Exeler, R Wittwer, B Horst, J
Citation: D. Meschede et al., Submicroscopic deletion in 14q32.3 through a de novo tandem translocation between 14q and 21p, AM J MED G, 80(5), 1998, pp. 443-447

Authors: Groen, SE Drewes, JG de Boer, EG Hoovers, JMN Hennekam, RCM
Citation: Se. Groen et al., Repeated unbalanced offspring due to a familial translocation involving chromosomes 5 and 6, AM J MED G, 80(5), 1998, pp. 448-453

Authors: Lukusa, T Fryns, JP
Citation: T. Lukusa et Jp. Fryns, Syndrome of facial, oral, and digital anomalies due to 7q21.2 -> q22.1 duplication, AM J MED G, 80(5), 1998, pp. 454-458

Authors: Castilla, EE Lugarinho, R Dutra, MD Salgado, LJ
Citation: Ee. Castilla et al., Associated anomalies in individuals with polydactyly, AM J MED G, 80(5), 1998, pp. 459-465

Authors: Feitosa, MF Castilla, EE Dutra, MD Krieger, H
Citation: Mf. Feitosa et al., Lack of evidence of a major gene acting on postaxial polydactyly in South America, AM J MED G, 80(5), 1998, pp. 466-472

Authors: Hsu, WT Shchepin, DA Mao, R Berry-Kravis, E Garber, AP Fischel-Ghodsian, N Falk, RE Carlson, DE Roeder, ER Leeth, EA Hajianpour, MJ Wang, JCC Rosenblum-Vos, LS Bhatt, SD Karson, EM Hux, CH Trunca, C Bialer, MG Linn, SK Schreck, RR
Citation: Wt. Hsu et al., Mosaic trisomy 16 ascertained through amniocentesis: Evaluation of 11 new cases, AM J MED G, 80(5), 1998, pp. 473-480

Authors: Attie-Bitach, T Abitbol, M Gerard, M Delezoide, AL Auge, J Pelet, A Amiel, J Pachnis, V Munnich, A Lyonnet, S Vekemans, M
Citation: T. Attie-bitach et al., Expression of the RET proto-oncogene in human embryos, AM J MED G, 80(5), 1998, pp. 481-486

Authors: Li, SB Tuck-Muller, CM Martinez, JE Rowley, ER Chen, H Wertelecki, W
Citation: Sb. Li et al., Prenatal detection of de novo duplication of the short arm of chromosome 18 confirmed by fluorescence in situ hybridization (FISH), AM J MED G, 80(5), 1998, pp. 487-490

Authors: Ounap, K Laidre, P Bartsch, O Rein, R Lipping-Sitska, M
Citation: K. Ounap et al., Familial Williams-Beuren syndrome, AM J MED G, 80(5), 1998, pp. 491-493

Authors: Kjaer, I Keeling, JW Reintoft, I Nolting, D Hansen, BF
Citation: I. Kjaer et al., Pituitary gland and Sella turcica in human trisomy 21 fetuses related to axial skeletal development, AM J MED G, 80(5), 1998, pp. 494-500

Authors: Atchaneeyasakul, LO Linck, LM Connor, WE Weleber, RG Steiner, RD
Citation: Lo. Atchaneeyasakul et al., Eye findings in 8 children and a spontaneously aborted fetus with RSH/Smith-Lemli-Opitz syndrome, AM J MED G, 80(5), 1998, pp. 501-505

Authors: Strenge, S Froster, UG
Citation: S. Strenge et Ug. Froster, Microcephaly-lymphedema syndrome: Report of a family with short stature asadditional manifestation, AM J MED G, 80(5), 1998, pp. 506-509

Authors: Deere, M Sanford, T Ferguson, HL Daniels, K Hecht, JT
Citation: M. Deere et al., Identification of twelve mutations in cartilage oligomeric matrix protein (COMP) in patients with pseudoachondroplasia, AM J MED G, 80(5), 1998, pp. 510-513

Authors: Daikha-Dahmane, F Huten, Y Morvan, J Szpiro-Tapia, S Nessmann, C Eydoux, P
Citation: F. Daikha-dahmane et al., Fetus with Casamassima-Morton-Nance syndrome and an inherited (6;9) balanced translocation, AM J MED G, 80(5), 1998, pp. 514-517

Authors: Mathew, A
Citation: A. Mathew, Anencephaly-associated aganglionosis, AM J MED G, 80(5), 1998, pp. 518-520

Authors: Erdmann, J Hegemann, N Weidemann, A Kallisch, H Hummel, M Hetzer, R Fleck, E Regitz-Zagrosek, V
Citation: J. Erdmann et al., Screening the human bradykinin B-2 receptor gene in patients with cardiovascular diseases: Identification of a functional mutation in the promoter and a new coding variant (T21M), AM J MED G, 80(5), 1998, pp. 521-525

Authors: Udler, Y Halpern, GJ Shohat, M Cohen, D
Citation: Y. Udler et al., Tsukahara syndrome of radioulnar synostosis, short stature, microcephaly, scoliosis, and mental retardation, AM J MED G, 80(5), 1998, pp. 526-528

Authors: Endo, A Watanabe, K Shimada, M Minato, M Takada, M Takahashi, S Harada, K
Citation: A. Endo et al., Bilateral involvement of hands and legs in the Gollop-Wolfgang complex, AM J MED G, 80(5), 1998, pp. 529-530

Authors: Swillen, A Devriendt, K Vantrappen, G Vogels, A Rommel, N Fryns, JP Eyskens, B Gewillig, M Dumoulin, M
Citation: A. Swillen et al., Familial deletions of chromosome 22q11: The Leuven experience, AM J MED G, 80(5), 1998, pp. 531-532

Authors: Schimke, RN Collins, DL Rothberg, PG
Citation: Rn. Schimke et al., Functioning carotid paraganglioma in the von Hippel-Lindau syndrome, AM J MED G, 80(5), 1998, pp. 533-534

Authors: de Silva, DC Verloes, A
Citation: Dc. De Silva et A. Verloes, Further delineation of the Verloes-Koulischer-Oro-Acral syndrome, AM J MED G, 80(5), 1998, pp. 535-537

Authors: Maroteaux, P Le Merrer, M
Citation: P. Maroteaux et M. Le Merrer, Bilateral Poland anomaly versus thoracic dysplasia, AM J MED G, 80(5), 1998, pp. 538-538

Authors: Karnak, I Tanyel, FC
Citation: I. Karnak et Fc. Tanyel, Reply to "Bilateral Poland anomaly versus thoracic dysplasia" by Maroteauxand Le Merrer, AM J MED G, 80(5), 1998, pp. 539-539

Authors: Danesino, C Pasquali, F Dellavecchia, C Maserati, E Minelli, A Seghezzi, L
Citation: C. Danesino et al., Constitutional trisomy 8 mosaicism: Mechanism of origin, phenotype variability, and risk of malignancies, AM J MED G, 80(5), 1998, pp. 540-540
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