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Results: 1-6 |
Results: 6

Authors: GUILLENNAVARRO E WALLERSTEIN R REICH E ZAJAC L OSTRER H
Citation: E. Guillennavarro et al., ACRO-RENAL-OCULAR SYNDROME - EXPANSION OF THE PHENOTYPE, Clinical dysmorphology, 7(4), 1998, pp. 243-248

Authors: GUILLENNAVARRO E WALLERSTEIN R MORAN E CHU ML GRANT A
Citation: E. Guillennavarro et al., A NEW FORM OF COMPLICATED HEREDITARY SPASTIC PARAPLEGIA WITH CATARACTS, ATRETIC EAR CANALS AND HYPOPIGMENTATION, Clinical neurology and neurosurgery, 100(1), 1998, pp. 64-67

Authors: GUILLENNAVARRO E WALLERSTEIN R REICH E ZAJAC L OSTRER H
Citation: E. Guillennavarro et al., ROBINOW-SYNDROME WITH DEVELOPMENTAL BRAIN DYSPLASIA, American journal of medical genetics, 73(1), 1997, pp. 98-99

Authors: GUILLENNAVARRO E CHAN WC RAGOUSSIS J DAVIES AF OSTRER H PERLE MA
Citation: E. Guillennavarro et al., A RARE DE-NOVO MICRODELETION OF DISTAL CHROMOSOME 6P - CLINICAL PHENOTYPE AND MOLECULAR CYTOGENETIC CHARACTERIZATION, American journal of human genetics, 61(4), 1997, pp. 719-719

Authors: HANLEY NA HAGAN DM OSTRER H GUILLENNAVARRO E WILSON DI BULLEN P LINDSAY S ROBSON S CLEMENTJONES M STRACHAN T
Citation: Na. Hanley et al., SPATIOTEMPORAL EXPRESSION PATTERNS OF THE SEX-DETERMINING GENES, SRY,SOX9, AND WT1, DURING EARLY HUMAN-DEVELOPMENT, American journal of human genetics, 61(4), 1997, pp. 878-878

Authors: ODDOUX C GUILLENNAVARRO E CLAYTON CM NELSON H PERETZ H SELIGSOHN U LUZZATTO L NARDI M KARPATKIN M DITIVOLI C DICAVE E AXELROD F OSTRER H
Citation: C. Oddoux et al., GENETIC-EVIDENCE FOR A COMMON ORIGIN AMONG ROMAN JEWS AND ASHKENAZI JEWS, American journal of human genetics, 61(4), 1997, pp. 1200-1200
Risultati: 1-6 |