Results: 1-25 | 26-50 | 51-75 | 76-100 | >>

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

Results: 1-25/705

Authors: Lin, AE Pierpont, MEM
Citation: Ae. Lin et Mem. Pierpont, Heart development and the genetic aspects of cardiovascular malformations, AM J MED G, 97(4), 2000, pp. 235-237

Authors: Opitz, JM Clark, EB
Citation: Jm. Opitz et Eb. Clark, Heart development: An introduction, AM J MED G, 97(4), 2000, pp. 238-247

Authors: Lohr, JL Yost, J
Citation: Jl. Lohr et J. Yost, Vertebrate model systems in the study of early heart development: Xenopus and zebrafish, AM J MED G, 97(4), 2000, pp. 248-257

Authors: Schneider, H Brueckner, M
Citation: H. Schneider et M. Brueckner, Of mice and men: Dissecting the genetic pathway that controls left-right asymmetry in mice and humans, AM J MED G, 97(4), 2000, pp. 258-270

Authors: Kathiriya, IS Srivastava, D
Citation: Is. Kathiriya et D. Srivastava, Left-right asymmetry and cardiac looping: Implications for cardiac development and congenital heart disease, AM J MED G, 97(4), 2000, pp. 271-279

Authors: Maschhoff, KL Baldwin, HS
Citation: Kl. Maschhoff et Hs. Baldwin, Molecular determinants of neural crest migration, AM J MED G, 97(4), 2000, pp. 280-288

Authors: Pierpont, MEM Markwald, RR Lin, AE
Citation: Mem. Pierpont et al., Genetic aspects of atrioventricular septal defects, AM J MED G, 97(4), 2000, pp. 289-296

Authors: Towbin, JA Belmont, J
Citation: Ja. Towbin et J. Belmont, Molecular determinants of left and right outflow tract obstruction, AM J MED G, 97(4), 2000, pp. 297-303

Authors: Vaughan, CJ Basson, CT
Citation: Cj. Vaughan et Ct. Basson, Molecular determinants of atrial and ventricular septal defects and patentductus arteriosus, AM J MED G, 97(4), 2000, pp. 304-309

Authors: Roberts, R Brugada, R
Citation: R. Roberts et R. Brugada, Genetic aspects of arrhythmias, AM J MED G, 97(4), 2000, pp. 310-318

Authors: Loffredo, CA
Citation: Ca. Loffredo, Epidemiology of cardiovascular malformations: Prevalence and risk factors, AM J MED G, 97(4), 2000, pp. 319-325

Authors: Neri, G Chiurazzi, P
Citation: G. Neri et P. Chiurazzi, X-linked mental retardation, AM J MED G, 97(3), 2000, pp. 173-173

Authors: Stevenson, RE
Citation: Re. Stevenson, Splitting and lumping in the nosology of XLMR, AM J MED G, 97(3), 2000, pp. 174-182

Authors: Willemsen, R Oostra, BA
Citation: R. Willemsen et Ba. Oostra, FMRP detection assay for the diagnosis of the fragile X syndrome, AM J MED G, 97(3), 2000, pp. 183-188

Authors: Sherman, SL
Citation: Sl. Sherman, Premature ovarian failure in the fragile X syndrome, AM J MED G, 97(3), 2000, pp. 189-194

Authors: Tassone, F Hagerman, RJ Chamberlain, WD Hagerman, PJ
Citation: F. Tassone et al., Transcription of the FMR1 gene in individuals with fragile X syndrome, AM J MED G, 97(3), 2000, pp. 195-203

Authors: Gibbons, RJ Higgs, DR
Citation: Rj. Gibbons et Dr. Higgs, Molecular-clinical spectrum of the ATR-X syndrome, AM J MED G, 97(3), 2000, pp. 204-212

Authors: Leventer, RJ Mills, PL Dobyns, WB
Citation: Rj. Leventer et al., X-linked malformations of cortical development, AM J MED G, 97(3), 2000, pp. 213-220

Authors: Toniolo, D
Citation: D. Toniolo, In search of the MRX genes, AM J MED G, 97(3), 2000, pp. 221-227

Authors: Neri, G Opitz, JM
Citation: G. Neri et Jm. Opitz, Sixty years of X-linked mental retardation: A historical footnote, AM J MED G, 97(3), 2000, pp. 228-233

Authors: Fisch, GS
Citation: Gs. Fisch, Psychology genetics, AM J MED G, 97(2), 2000, pp. 109-111

Authors: Ozonoff, S Williams, BJ Rauch, AM Opitz, JM
Citation: S. Ozonoff et al., Behavior phenotype of FG syndrome: Cognition, personality, and behavior ineleven affected boys, AM J MED G, 97(2), 2000, pp. 112-118

Authors: North, K
Citation: K. North, Neurofibromatosis type 1, AM J MED G, 97(2), 2000, pp. 119-127

Authors: Swillen, A Vogels, A Devriendt, K Fryns, JP
Citation: A. Swillen et al., Chromosome 22q11 deletion syndrome: Update and review of the clinical features, cognitive-behavioral spectrum, and psychiatric complications, AM J MED G, 97(2), 2000, pp. 128-135

Authors: Cassidy, SB Dykens, E Williams, CA
Citation: Sb. Cassidy et al., Prader-Willi and Angelman Syndromes: Sister imprinted disorders, AM J MED G, 97(2), 2000, pp. 136-146
Risultati: 1-25 | 26-50 | 51-75 | 76-100 | >>