Rational usage of therapeutic drug monitoring in antiepileptic treatment H. Bartels Review Pages: 193 - 199
Monodactylous splithand-splitfoot Györgyi BujdosoWidukind Lenz Original Investigations Pages: 207 - 215
The ECP syndrome, another autosomal dominant cause of monodactylous ectrodactyly John M. OpitzJ. L. FriasM. M. Cohen Jr. Original Investigations Pages: 217 - 220
Tetraectrodactyly and other skeletal manifestations in the fetal alcohol syndrome Jürgen HerrmannPhilip D. PallisterJohn M. Opitz Original Investigations Pages: 221 - 226
The mild form of pseudoachondroplasia P. MaroteauxR. StanescuG. Fontaine Original Investigations Pages: 227 - 231
Moderate alcohol consumption during pregnancy and child development G. Mau Original Investigations Pages: 233 - 237
Autosomal dominant inheritance of hypercalciuria K. MéhesZs. Szelid Original Investigations Pages: 239 - 242
Minor craniofacial anomalies in children G. NeuhäuserJ. Vogl Original Investigations Pages: 243 - 250
Prolactin secretion in 70 patients with growth hormone deficiency Abraham RoitmanSara AssaZvi Laron Original Investigations Pages: 251 - 258
17-Hydroxyprogesterone, androstenedione, and testosterone in normal children and in prepubertal patients with congenital adrenal hyperplasia K. v. SchnakenburgF. BidlingmaierD. Knorr Original Investigations Pages: 259 - 267
Urinary oligosaccharide screening in patients with β-galactosidase deficiency A. C. SewellJ. GehlerJ. Spranger Original Investigations Pages: 269 - 271
Serum concentrations of vitamin E in healthy infants fed commercial milks C. SimonD. KioszI. Hoffmann Original Investigations Pages: 273 - 276
Anthropometric measurements in patients with growth hormone deficiency before treatment with human growth hormone M. ZachmannF. FernandezA. Prader Original Investigations Pages: 277 - 282
Congenital adrenal hyperplasia associated with a balanced 13–18 translocation Frank PetersenFinn Ursin KnudsenMargareta Mikkelsen Case Reports Pages: 283 - 285
Goldenhar syndrome and hemifacial microsomia: Observations on three patients Peter Thomas Case Reports Pages: 287 - 292
Male infant with cat cry syndrome and apparent absence of the Y chromosome M. TolksdorfJ. KunzeH. Chiyo Case Reports Pages: 293 - 296
Phenylketonuria and neonatal hypothyroidism in Spain. Priority of screening for neonatal hypothyroidism P. Frontera-Izquierdo Letter to the Editor Pages: 297 - 297