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Results: 1-12 |
Results: 12
FURTHER EVIDENCE THAT THE HAJDU-CHENEY-SYNDROME AND THE SERPENTINE FIBULA POLYCYSTIC KIDNEY SYNDROME ARE A SINGLE ENTITY
Authors: RAMOS FJ KAPLAN BS BELLAH RD ZACKAI EH KAPLAN P
Citation: Fj. Ramos et al., FURTHER EVIDENCE THAT THE HAJDU-CHENEY-SYNDROME AND THE SERPENTINE FIBULA POLYCYSTIC KIDNEY SYNDROME ARE A SINGLE ENTITY, American journal of medical genetics, 78(5), 1998, pp. 474-481
SEVERE MALFORMATIONS IN MALES FROM FAMILIES WITH OSTEOPATHIA STRIATA WITH CRANIAL SCLEROSIS
Authors: BUENO AL RAMOS FJ BUENO O OLIVARES JL BELLO ML BUENO M
Citation: Al. Bueno et al., SEVERE MALFORMATIONS IN MALES FROM FAMILIES WITH OSTEOPATHIA STRIATA WITH CRANIAL SCLEROSIS, Clinical genetics, 54(5), 1998, pp. 400-405
SEASONALITY OF CRYPTOSPORIDIOSIS IN CHILDREN
Authors: CLAVEL A OLIVARES JL FLETA J CASTILLO J VAREA M RAMOS FJ ARNAL AC QUILEZ J
Citation: A. Clavel et al., SEASONALITY OF CRYPTOSPORIDIOSIS IN CHILDREN, European journal of clinical microbiology & infectious diseases, 15(1), 1996, pp. 77-79
ON THE TIME OF SIGNS - SPANISH - FORASTIE RIBRASCHI,E
Authors: RAMOS FJ
Citation: Fj. Ramos, ON THE TIME OF SIGNS - SPANISH - FORASTIE RIBRASCHI,E, Confluencia, 11(2), 1996, pp. 275-280
A GIRL WITH BRANCHIOOTORENAL SYNDROME (BOR) AND SEVERE MENTAL-RETARDATION
Authors: RAMOS FJ LOPEZ MJ BUENO I OLIVARES JL LOPEZPISON J BUENO M
Citation: Fj. Ramos et al., A GIRL WITH BRANCHIOOTORENAL SYNDROME (BOR) AND SEVERE MENTAL-RETARDATION, American journal of human genetics, 57(4), 1995, pp. 1780-1780
THE PARADOX OF THE G-CSF
Authors: RAMOS FJ SANDOVAL V RODRIGUEZ JA MORO MJ
Citation: Fj. Ramos et al., THE PARADOX OF THE G-CSF, Medicina Clinica, 102(18), 1994, pp. 718-719
SCLEROSTEOSIS IN A SPANISH MALE - FIRST REPORT IN A PERSON OF MEDITERRANEAN ORIGIN
Authors: BUENO M OLIVAN G JIMENEZ A GARAGORRI JM SARRIA A BUENO AL BUENO M RAMOS FJ
Citation: M. Bueno et al., SCLEROSTEOSIS IN A SPANISH MALE - FIRST REPORT IN A PERSON OF MEDITERRANEAN ORIGIN, Journal of Medical Genetics, 31(12), 1994, pp. 976-977
SAETHRE-CHOTZEN SYNDROME WITH FAMILIAL TRANSLOCATION AT CHROMOSOME 7P22
Authors: REID CS MCMORROW LE MCDONALDMCGINN DM GRACE KJ RAMOS FJ ZACKAI EH COHEN MM JABS EW
Citation: Cs. Reid et al., SAETHRE-CHOTZEN SYNDROME WITH FAMILIAL TRANSLOCATION AT CHROMOSOME 7P22, American journal of medical genetics, 47(5), 1993, pp. 637-639
NAIL-PATELLA SYNDROME WITH CRANIOSYNOSTOSIS AND MYOPATHY - A NEW ASSOCIATION
Authors: RAMOS FJ NICHOLSON L MARKS HG SCOTT CI
Citation: Fj. Ramos et al., NAIL-PATELLA SYNDROME WITH CRANIOSYNOSTOSIS AND MYOPATHY - A NEW ASSOCIATION, American journal of human genetics, 53(3), 1993, pp. 491-491
INFORMATIVE, FLANKING CA-REPEAT POLYMORPHISMS FOR LINKAGE ANALYSIS OFFAMILIES WITH AUTOSOMAL SPINAL MUSCULAR-ATROPHY
Authors: KANT JA BUENO M RAMOS FJ
Citation: Ja. Kant et al., INFORMATIVE, FLANKING CA-REPEAT POLYMORPHISMS FOR LINKAGE ANALYSIS OFFAMILIES WITH AUTOSOMAL SPINAL MUSCULAR-ATROPHY, American journal of human genetics, 53(3), 1993, pp. 1180-1180
FEATURES MOST COMMONLY ASSOCIATED WITH X-LINKED SPINAL BULBAR MUSCULAR-ATROPHY - DELINEATION BY MOLECULAR ANALYSIS
Authors: HOSHI N RAMOS FJ LASPADA AR FISCHBECK KH KANT JA
Citation: N. Hoshi et al., FEATURES MOST COMMONLY ASSOCIATED WITH X-LINKED SPINAL BULBAR MUSCULAR-ATROPHY - DELINEATION BY MOLECULAR ANALYSIS, American journal of human genetics, 53(3), 1993, pp. 1731-1731
DIRECT DNA TESTING FOR FRAGILE-X SYNDROME
Authors: RAMOS FJ EUNPU DL FINUCANE B PFENDNER EG
Citation: Fj. Ramos et al., DIRECT DNA TESTING FOR FRAGILE-X SYNDROME, American journal of diseases of children [1960], 147(11), 1993, pp. 1231-1235
Risultati: 1-12 |