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Results: 1-8 |
Results: 8

Authors: KRESS W MELCHER R HALLIGERKELLER B COLLMANN H
Citation: W. Kress et al., MUTATIONS IN SAETHRE-CHOTZEN-SYNDROME, European journal of human genetics, 6, 1998, pp. 1138-1138

Authors: ELSNER HA HORWITZ EA KELLNER MW COLLMANN H HAHN D
Citation: Ha. Elsner et al., ABDOMINAL ULTRASOUND IN CHILDREN WITH VENTRICULOPERITONEAL SHUNT - A DECISION HELP FOR SHUNT REVISION, Radiology, 209P, 1998, pp. 650-650

Authors: STEINBERGER D COLLMANN H SCHMALENBERGER B MULLER U
Citation: D. Steinberger et al., A NOVEL MUTATION (A886G) IN EXON-5 OF FGFR2 IN MEMBERS OF A FAMILY WITH CROUZON PHENOTYPE AND PLAGIOCEPHALY, Journal of Medical Genetics, 34(5), 1997, pp. 420-422

Authors: LIEB G KRAUSS J COLLMANN H SCHROD L SORENSEN N
Citation: G. Lieb et al., RECURRENT BACTERIAL-MENINGITIS, European journal of pediatrics, 155(1), 1996, pp. 26-30

Authors: COLLMANN H SORENSEN N KRAUSS J
Citation: H. Collmann et al., CONSENSUS - TRIGONOCEPHALY, Child's nervous system, 12(11), 1996, pp. 664-668

Authors: REINHART E MUHLING J MICHEL C COLLMANN H PISTNER H REUTHER J
Citation: E. Reinhart et al., CRANIOFACIAL GROWTH-CHARACTERISTICS AFTER BILATERAL FRONTO-ORBITAL ADVANCEMENT IN CHILDREN WITH PREMATURE CRANIOSYNOSTOSIS, Child's nervous system, 12(11), 1996, pp. 690-694

Authors: COLLMANN H
Citation: H. Collmann, READERS ASK - EXPERTS ANSWER - CURRENT TR EATMENT FOR CEREBRAL HEMORRHAGES WITH VENTRICULAR DILATION IN PRETERM NEONATES, Monatsschrift fur Kinderheilkunde, 143(6), 1995, pp. 618-619

Authors: STRASSBURG HM FECH M COLLMANN H BUESSE M
Citation: Hm. Strassburg et al., EEG IN PEDIATRIC-PATIENTS WITH CRANIOSYNOSTOSIS SYNDROMES, Epilepsia, 36, 1995, pp. 78-79
Risultati: 1-8 |