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Authors: MORELLI SH PYSHER TJ GILBERTBARNESS EF OPITZ JM VISKOCHIL DH
Citation: Sh. Morelli et al., PATHOGENESIS OF SIRENOMELIA WITH ANENCEPHALY AND OTHER MIDLINE DEFECTS, Journal of investigative medicine, 46(1), 1998, pp. 119-119

Authors: OSEBOLD WR POZNANSKI AK OPITZ JM LANGER LO SPRANGER JW UNNI KK
Citation: Wr. Osebold et al., PREVIOUSLY UNDESCRIBED SYNDROME OF SPONDYLOMETAPHYSEAL DYSPLASIA, OSTEOCARTILAGINOUS METAPLASIA OF LONG BONES, AND PROGRESSIVE OSTEOLYSIS OF DISTAL PHALANGES, American journal of medical genetics, 80(3), 1998, pp. 187-195

Authors: OPITZ JM WEAVER DW REYNOLDS JF
Citation: Jm. Opitz et al., THE SYNDROMES OF SOTOS AND WEAVER - REPORTS AND REVIEW, American journal of medical genetics, 79(4), 1998, pp. 294-304

Authors: RAUCH A OPITZ JM WALKER D
Citation: A. Rauch et al., SYNDROMAL FORAMINA PARIETALIA PERMAGNA - NEW OR FG SYNDROME - COMMENTS ON THE PAPER BY CHRZANOWSKA ET-AL. [1998], American journal of medical genetics, 78(5), 1998, pp. 406-407

Authors: OPITZ JM MULLEN P
Citation: Jm. Opitz et P. Mullen, TIMEO DANAOS, American journal of medical genetics, 78(5), 1998, pp. 487-488

Authors: MARTINEZFRIAS ML FRIAS JL OPITZ JM
Citation: Ml. Martinezfrias et al., ERRORS OF MORPHOGENESIS AND DEVELOPMENTAL FIELD-THEORY, American journal of medical genetics, 76(4), 1998, pp. 291-296

Authors: CARRANZA A GILBERTBARNESS E MADRIGAL F OPITZ JM
Citation: A. Carranza et al., COMPLETE ABSENCE OR DEFICIENCY OF ONE HALF OF THE BODY, American journal of medical genetics, 76(3), 1998, pp. 197-201

Authors: TSUKAHARA M FUJISAWA K YAMAMOTO K YAMAMAKA T HASUI M HONDA A HONDA M TINT GS SALEN G SAITO C OPITZ JM
Citation: M. Tsukahara et al., SMITH-LEMLI-OPITZ-SYNDROME IN JAPAN, American journal of medical genetics, 75(1), 1998, pp. 118-119

Authors: GAUDENZ K ROESSLER E QUADERI N FRANCO B FELDMAN G GASSER DL WITTWER B HORST J MONTINI E OPITZ JM BALLABIO A MUENKE M
Citation: K. Gaudenz et al., OPITZ G BBB SYNDROME IN XP22 - MUTATIONS IN THE MID1 GENE-CLUSTER IN THE CARBOXY-TERMINAL DOMAIN (VOL 63, PG 703, 1998)/, American journal of human genetics, 63(5), 1998, pp. 1571-1571

Authors: GAUDENZ K ROESSLER E QUADERI N FRANCO B FELDMAN G GASSER DL WITTWER B MONTINI E OPITZ JM BALLABIO A MUENKE M
Citation: K. Gaudenz et al., OPITZ G BBB SYNDROME IN XP22 - MUTATIONS IN THE MID1 GENE-CLUSTER IN THE CARBOXY-TERMINAL DOMAIN/, American journal of human genetics, 63(3), 1998, pp. 703-710

Authors: QUADERI NA SCHWEIGER S GAUDENZ K FRANCO B RUGARLI EI BERGER W FELDMAN GJ VOLTA M ANDOLFI G GILGENKRANTZ S MARION RW HENNEKAM RCM OPITZ JM MUENKE M ROPERS HH BALLABIO A
Citation: Na. Quaderi et al., OPITZ G BBB SYNDROME, A DEFECT OF MIDLINE DEVELOPMENT, IS DUE TO MUTATIONS IN A NEW RING FINGER GENE ON XP22/, Nature genetics, 17(3), 1997, pp. 285-291

Authors: BELOUSSOV LV OPITZ JM GILBERT SF
Citation: Lv. Beloussov et al., LIFE OF GURWITSCH,ALEXANDER,G. AND HIS RELEVANT CONTRIBUTION TO THE THEORY OF MORPHOGENETIC FIELDS, The International journal of developmental biology, 41(6), 1997, pp. 771-777

Authors: OPITZ JM GILBERT SF
Citation: Jm. Opitz et Sf. Gilbert, LIFE OF GURWITSCH,ALEXANDER,G. AND HIS RELEVANT CONTRIBUTION TO THE THEORY OF MORPHOGENETIC FIELDS - COMMENTARY, The International journal of developmental biology, 41(6), 1997, pp. 778-779

Authors: PAVONE L SORGE G PAVONE V RIZZO R RUGGIERI M POLIZZI A OPITZ JM
Citation: L. Pavone et al., FAMILIAL BROAD TERMINAL PHALANGES WITH ONE INDIVIDUAL SHOWING ADDITIONAL ANOMALIES, American journal of medical genetics, 71(3), 1997, pp. 271-274

Authors: SORGE G PAVONE L POLIZZI A MAUCERI L LEONARDI RM TRIPI T OPITZ JM
Citation: G. Sorge et al., ANOTHER NEW FORM, THE PALAGONIA TYPE OF ACROFACIAL DYSOSTOSIS IN A SICILIAN FAMILY, American journal of medical genetics, 69(4), 1997, pp. 388-394

Authors: OPITZ JM
Citation: Jm. Opitz, MOVING FORWARD, American journal of medical genetics, 69(2), 1997, pp. 3-4

Authors: OPITZ JM
Citation: Jm. Opitz, NEUROLOGIC ABNORMALITIES IN THE SKELETAL DYSPLASIAS - A CLINICAL AND RADIOLOGICAL PERSPECTIVE - COMMENT, American journal of medical genetics, 69(1), 1997, pp. 44-44

Authors: OPITZ JM
Citation: Jm. Opitz, REPLY TO DR ALLANSON AND CO-AUTHORS REGARDING CLINICAL ILLUSTRATIONS IN THE AMERICAN-JOURNAL-OF-MEDICAL-GENETICS, American journal of medical genetics, 68(4), 1997, pp. 488-488

Authors: RIZZO R PAVONE V CORSELLO G SORGE G NERI G OPITZ JM
Citation: R. Rizzo et al., AUTOSOMAL-DOMINANT AND SPORADIC RADIOULNAR SYNOSTOSIS, American journal of medical genetics, 68(2), 1997, pp. 127-134

Authors: OPITZ JM JOHNSON JP NERI G NIIKAWA N
Citation: Jm. Opitz et al., WITH GRATITUDE TO THE ANONYMOUS REVIEWERS, American journal of medical genetics, 66(4), 1996, pp. 485-492

Authors: CORSELLO G ALBANESE A PICCIONE M GIUFFRE M OPITZ JM
Citation: G. Corsello et al., AUTOSOMAL RECESSIVE SEVERE DWARFISM IN A SICILIAN GIRL - A NEW FORM OF OSTEODYSPLASTIC PRIMORDIAL DWARFISM, American journal of medical genetics, 66(3), 1996, pp. 265-268

Authors: OPITZ JM WIEDEMANN HR
Citation: Jm. Opitz et Hr. Wiedemann, IN-MEMORIAM - LENZ,WIDUKIND, 1919-1995, American journal of medical genetics, 65(2), 1996, pp. 142-145

Authors: VIANNAMORGANTE AM AZEVEDO ES OTTO PA OPITZ JM
Citation: Am. Viannamorgante et al., ENCOMIUM - FROTAPESSOA,OSWALDO, American journal of medical genetics, 63(4), 1996, pp. 581-584

Authors: OPITZ JM
Citation: Jm. Opitz, IN HONOR OF SPRANGER,JURGEN AT 65, American journal of medical genetics, 63(1), 1996, pp. 1-2

Authors: GILBERTBARNES E LANGER LO OPITZ JM LAXOVA R SOTELOARILA C
Citation: E. Gilbertbarnes et al., KNIEST DYSPLASIA - RADIOLOGIC, HISTOPATHOLOGICAL, AND SCANNING ELECTRON-MICROSCOPIC FINDINGS, American journal of medical genetics, 63(1), 1996, pp. 34-45
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