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Results: 1-11 |
Results: 11
SPECTRUM OF MALIGNANCY AND PREMALIGNANCY IN CARNEY-SYNDROME
Authors: NWOKORO NA KORYTKOWSKI MT ROSE S GORIN MB STADLER MP WITCHEL SF MULVIHILL JJ
Citation: Na. Nwokoro et al., SPECTRUM OF MALIGNANCY AND PREMALIGNANCY IN CARNEY-SYNDROME, American journal of medical genetics, 73(4), 1997, pp. 369-377
CHOLESTEROL AND BILE-ACID REPLACEMENT THERAPY IN CHILDREN AND ADULTS WITH SMITH-LEMLI-OPITZ (SLO RSH) SYNDROME/
Authors: NWOKORO NA MULVIHILL JJ
Citation: Na. Nwokoro et Jj. Mulvihill, CHOLESTEROL AND BILE-ACID REPLACEMENT THERAPY IN CHILDREN AND ADULTS WITH SMITH-LEMLI-OPITZ (SLO RSH) SYNDROME/, American journal of medical genetics, 68(3), 1997, pp. 315-321
CROUZON SYNDROME - MUTATIONS IN 2 SPLICEOFORMS OF FGFR2 AND A COMMON POINT MUTATION SHARED WITH JACKSON-WEISS SYNDROME
Authors: GORRY MC PRESTON RA WHITE GJ ZHANG YZ SINGHAL VK LOSKEN HW PARKER MG NWOKORO NA POST JC EHRLICH GD
Citation: Mc. Gorry et al., CROUZON SYNDROME - MUTATIONS IN 2 SPLICEOFORMS OF FGFR2 AND A COMMON POINT MUTATION SHARED WITH JACKSON-WEISS SYNDROME, Human molecular genetics, 4(8), 1995, pp. 1387-1390
10Q26 - CONSISTENT CHROMOSOMAL BREAKPOINT IN 2 CARDIAC MYXOMAS FROM APATIENT WITH CARNEY-SYNDROME
Authors: GOLLIN SM JENKINS RB SWANEY WP MULVIHILL JJ BARTELT D NWOKORO NA
Citation: Sm. Gollin et al., 10Q26 - CONSISTENT CHROMOSOMAL BREAKPOINT IN 2 CARDIAC MYXOMAS FROM APATIENT WITH CARNEY-SYNDROME, American journal of human genetics, 57(4), 1995, pp. 343-343
CONCORDANCE OF CLINICAL FINDINGS IN SIBLINGS WITH THE SMITH-LEMLI-OPITZ SYNDROME
Authors: CUNNIFF CM ABUELO DN ARN PH BARNSHAD MJ CAREY JC NWOKORO NA MULVIHILL JJ ZACKAI EH KELLEY RI
Citation: Cm. Cunniff et al., CONCORDANCE OF CLINICAL FINDINGS IN SIBLINGS WITH THE SMITH-LEMLI-OPITZ SYNDROME, American journal of human genetics, 57(4), 1995, pp. 471-471
SMITH-LEMLI-OPITZ SYNDROME - BIOCHEMICAL BEFORE CLINICAL-DIAGNOSIS - EARLY DIETARY-MANAGEMENT
Authors: NWOKORO NA HYDE B MULVIHILL JJ
Citation: Na. Nwokoro et al., SMITH-LEMLI-OPITZ SYNDROME - BIOCHEMICAL BEFORE CLINICAL-DIAGNOSIS - EARLY DIETARY-MANAGEMENT, American journal of medical genetics, 50(4), 1994, pp. 375-376
CYTOGENETIC CHARACTERIZATION OF CAT EYE SYNDROME MARKER CHROMOSOME
Authors: WENGER SL SURTI U NWOKORO NA STEELE MW
Citation: Sl. Wenger et al., CYTOGENETIC CHARACTERIZATION OF CAT EYE SYNDROME MARKER CHROMOSOME, Annales de genetique, 37(1), 1994, pp. 33-36
BALLER-GEROLD SYNDROME - A POSTMORTEM EXAMINATION
Authors: NWOKORO NA JAFFE R BARMADA M
Citation: Na. Nwokoro et al., BALLER-GEROLD SYNDROME - A POSTMORTEM EXAMINATION, American journal of medical genetics, 47(8), 1993, pp. 1233-1233
THE BROADENED SPECTRUM OF MALIGNANCY AND PREMALIGNANCY IN THE CARNEY COMPLEX
Authors: STADLER MP NWOKORO NA KORYTKOWSKI MT ROSE S BANSAL V MULVIHILL JJ
Citation: Mp. Stadler et al., THE BROADENED SPECTRUM OF MALIGNANCY AND PREMALIGNANCY IN THE CARNEY COMPLEX, American journal of human genetics, 53(3), 1993, pp. 369-369
A GENE FOR SAETHRE-CHOTZEN SYNDROME ON CHROMOSOME 10P
Authors: MULVIHILL JJ OWEN J LOSKEN HW SURTI U JUDA SA ELSTER B NWOKORO NA
Citation: Jj. Mulvihill et al., A GENE FOR SAETHRE-CHOTZEN SYNDROME ON CHROMOSOME 10P, American journal of human genetics, 53(3), 1993, pp. 477-477
CLINICAL, CYTOGENETIC AND MOLECULAR CHARACTERIZATION OF FAMILIAL CAT-EYE SYNDROME WITH BILIARY ATRESIA AND OTHER ANEUPLOIDY
Authors: NWOKORO NA SCOTT J CALLIFDALEY F WENGER SL MULVIHILL JJ CHAKRAVARTI A
Citation: Na. Nwokoro et al., CLINICAL, CYTOGENETIC AND MOLECULAR CHARACTERIZATION OF FAMILIAL CAT-EYE SYNDROME WITH BILIARY ATRESIA AND OTHER ANEUPLOIDY, American journal of human genetics, 53(3), 1993, pp. 585-585
Risultati: 1-11 |