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Results: 1-7 |
Results: 7
A NOVEL MISSENSE MUTATION (S18N) IN THE 5'-NON-HMG BOX REGION OF THE SRY GENE IN A PATIENT WITH PARTIAL GONADAL-DYSGENESIS AND HIS NORMAL-MALE RELATIVES
Authors: DOMENICE S NISHI MY BILLERBECK AEC LATRONICO AC MEDEIROS MA RUSSELL AJ VASS K CARVALHO FM FRADE EMC ARNHOLD IJP MENDONCA BB
Citation: S. Domenice et al., A NOVEL MISSENSE MUTATION (S18N) IN THE 5'-NON-HMG BOX REGION OF THE SRY GENE IN A PATIENT WITH PARTIAL GONADAL-DYSGENESIS AND HIS NORMAL-MALE RELATIVES, Human genetics, 102(2), 1998, pp. 213-215
DETECTION OF LEPTOSPIRA DNA IN PATIENTS WITH ASEPTIC-MENINGITIS BY PCR
Authors: ROMERO EC BILLERBECK AEC LANDO VS CAMARGO ED SOUZA CC YASUDA PH
Citation: Ec. Romero et al., DETECTION OF LEPTOSPIRA DNA IN PATIENTS WITH ASEPTIC-MENINGITIS BY PCR, Journal of clinical microbiology, 36(5), 1998, pp. 1453-1455
CLINICAL, PATHOLOGICAL, AND MOLECULAR STUDIES OF 2 FAMILIES WITH IODIDE ORGANIFICATION DEFECT
Authors: REGO KGM BILLERBECK AEC TARGOVNIK HM SANTOS CLS ALKMIN MG BARBOSA S CAMARGO R MEDEIROSNETO G
Citation: Kgm. Rego et al., CLINICAL, PATHOLOGICAL, AND MOLECULAR STUDIES OF 2 FAMILIES WITH IODIDE ORGANIFICATION DEFECT, Endocrine pathology, 8(1), 1997, pp. 37-47
MOLECULAR ANALYSIS OF SEX DETERMINATION IN SEX-REVERSED AND TRUE HERMAPHRODITISM
Authors: COPELLI SB BERGADA C BILLERBECK AEC GOLDBERG AC KALIL J DAMIANI D TARGOVNIK HM
Citation: Sb. Copelli et al., MOLECULAR ANALYSIS OF SEX DETERMINATION IN SEX-REVERSED AND TRUE HERMAPHRODITISM, Brazilian journal of medical and biological research, 29(6), 1996, pp. 743-748
A 138-NUCLEOTIDE DELETION IN THE THYROGLOBULIN RIBONUCLEIC-ACID MESSENGER IN A CONGENITAL GOITER WITH DEFECTIVE THYROGLOBULIN SYNTHESIS
Authors: TARGOVNIK HM VONO J BILLERBECK AEC CERRONE GE VARELA V MENDIVE F WAJCHENBERG BL MEDEIROSNETO G
Citation: Hm. Targovnik et al., A 138-NUCLEOTIDE DELETION IN THE THYROGLOBULIN RIBONUCLEIC-ACID MESSENGER IN A CONGENITAL GOITER WITH DEFECTIVE THYROGLOBULIN SYNTHESIS, The Journal of clinical endocrinology and metabolism, 80(11), 1995, pp. 3356-3360
CLINICAL AND MOLECULAR-GENETICS STUDIES IN PENDREDS-SYNDROME
Authors: BILLERBECK AEC CAVALIERE H GOLDBERG AC KALIL J MEDEIROSNETO G
Citation: Aec. Billerbeck et al., CLINICAL AND MOLECULAR-GENETICS STUDIES IN PENDREDS-SYNDROME, Thyroid, 4(3), 1994, pp. 279-284
DEFECTIVE ORGANIFICATION OF IODIDE CAUSING HEREDITARY GOITROUS HYPOTHYROIDISM
Authors: MEDEIROSNETO GA BILLERBECK AEC WAJCHENBERG BL TARGOVNIK HM
Citation: Ga. Medeirosneto et al., DEFECTIVE ORGANIFICATION OF IODIDE CAUSING HEREDITARY GOITROUS HYPOTHYROIDISM, Thyroid, 3(2), 1993, pp. 143-159
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