AAAAAA

   
Results: 1-13 |
Results: 13
THE AFRICAN ORIGIN OF THE COMMON MUTATION IN AFRICAN-AMERICAN PATIENTS WITH GLYCOGEN-STORAGE-DISEASE TYPE-II
Authors: BECKER JA VLACH J RABEN N NAGARAJU K ADAMS EM HERMANS MM REUSER AJJ BROOKS SS TIFFT CJ HIRSCHHORN R HUIE ML NICOLINO M PLOTZ PH
Citation: Ja. Becker et al., THE AFRICAN ORIGIN OF THE COMMON MUTATION IN AFRICAN-AMERICAN PATIENTS WITH GLYCOGEN-STORAGE-DISEASE TYPE-II, American journal of human genetics, 62(4), 1998, pp. 991-994
BONE-MARROW TRANSPLANTATION PROLONGS LIFE-SPAN AND AMELIORATES NEUROLOGIC MANIFESTATIONS IN SANDHOFF DISEASE MICE
Authors: NORFLUS F TIFFT CJ MCDONALD MP GOLDSTEIN G CRAWLEY JN HOFFMANN A SANDHOFF K SUZUKI K PROIA RL
Citation: F. Norflus et al., BONE-MARROW TRANSPLANTATION PROLONGS LIFE-SPAN AND AMELIORATES NEUROLOGIC MANIFESTATIONS IN SANDHOFF DISEASE MICE, The Journal of clinical investigation, 101(9), 1998, pp. 1881-1888
TESTING FOR INTERACTION BETWEEN MATERNAL SMOKING AND TGFA GENOTYPE AMONG ORAL CLEFT CASES BORN IN MARYLAND 1992-1996
Authors: BEATY TH MAESTRI NE HETMANSKI JB WYSZYNSKI DF VANDERKOLK CA SIMPSON JC MCINTOSH I SMITH EA ZEIGER JS RAYMOND GV PANNY SR TIFFT CJ LEWANDA AF CRISTION CA WULFSBERG EA
Citation: Th. Beaty et al., TESTING FOR INTERACTION BETWEEN MATERNAL SMOKING AND TGFA GENOTYPE AMONG ORAL CLEFT CASES BORN IN MARYLAND 1992-1996, The Cleft palate-craniofacial journal, 34(5), 1997, pp. 447-454
THE BETA-HEXOSAMINIDASE DEFICIENCY DISORDERS - DEVELOPMENT OF A CLINICAL PARADIGM IN THE MOUSE
Authors: TIFFT CJ PROIA RL
Citation: Cj. Tifft et Rl. Proia, THE BETA-HEXOSAMINIDASE DEFICIENCY DISORDERS - DEVELOPMENT OF A CLINICAL PARADIGM IN THE MOUSE, Annals of medicine, 29(6), 1997, pp. 557-561
CRANIAL MAGNETIC-RESONANCE FINDINGS AND THE NEURODEVELOPMENTAL PERFORMANCE IN THE YOUNG-CHILD WITH NEUROFIBROMATOSIS TYPE-1
Authors: SAMANGOSPROUSE C VEZINA LG BRASSEUX C TILLMAN S TIFFT CJ
Citation: C. Samangosprouse et al., CRANIAL MAGNETIC-RESONANCE FINDINGS AND THE NEURODEVELOPMENTAL PERFORMANCE IN THE YOUNG-CHILD WITH NEUROFIBROMATOSIS TYPE-1, American journal of human genetics, 61(4), 1997, pp. 178-178
CONGENITAL BILATERAL PERISYLVIAN SYNDROME (CBPS) IN A CHILD WITH 47,XYY KARYOTYPE
Authors: GROPMAN AL SAMANGOSPROUSE C VEZINA LG TIFFT CJ
Citation: Al. Gropman et al., CONGENITAL BILATERAL PERISYLVIAN SYNDROME (CBPS) IN A CHILD WITH 47,XYY KARYOTYPE, American journal of human genetics, 61(4), 1997, pp. 2156-2156
MICE LACKING BOTH SUBUNITS OF LYSOSOMAL BETA-HEXOSAMINIDASE DISPLAY GANGLIOSIDOSIS AND MUCOPOLYSACCHARIDOSIS
Authors: SANGO K MCDONALD MP CRAWLEY JN MACK ML TIFFT CJ SKOP E STARR CM HOFFMANN A SANDHOFF K SUZUKI K PROIA RL
Citation: K. Sango et al., MICE LACKING BOTH SUBUNITS OF LYSOSOMAL BETA-HEXOSAMINIDASE DISPLAY GANGLIOSIDOSIS AND MUCOPOLYSACCHARIDOSIS, Nature genetics, 14(3), 1996, pp. 348-352
IDENTIFICATION OF DOMAINS IN HUMAN BETA-HEXOSAMINIDASE THAT DETERMINESUBSTRATE-SPECIFICITY
Authors: PENNYBACKER M LIESSEM B MOCZALL H TIFFT CJ SANDHOFF K PROIA RL
Citation: M. Pennybacker et al., IDENTIFICATION OF DOMAINS IN HUMAN BETA-HEXOSAMINIDASE THAT DETERMINESUBSTRATE-SPECIFICITY, The Journal of biological chemistry, 271(29), 1996, pp. 17377-17382
NEURODEVELOPMENTAL PROFILE OF INFANTS AND TODDLERS WITH OCULO-AURICULO-VERTEBRAL SPECTRUM AND THE CORRELATION OF PROGNOSIS WITH PHYSICAL FINDINGS
Authors: COHEN MS SAMANGOSPROUSE C STERN HJ CUSTER DA VAUGHT DR SAAL HM TIFFT CJ ROSENBAUM KN
Citation: Ms. Cohen et al., NEURODEVELOPMENTAL PROFILE OF INFANTS AND TODDLERS WITH OCULO-AURICULO-VERTEBRAL SPECTRUM AND THE CORRELATION OF PROGNOSIS WITH PHYSICAL FINDINGS, American journal of medical genetics, 60(6), 1995, pp. 535-540
RACIAL-DIFFERENCES IN THE PREVALENCE OF OPTIC-NERVE GLIOMAS IN NEUROFIBROMATOSIS TYPE
Authors: SAAL HM SCHORRY EK LOVELL AM BALL W EGELHOFF J KOCH B SAMANGOSPROUSE A ROSENBAUM KN STERN HJ TIFFT CJ VEZINA LG
Citation: Hm. Saal et al., RACIAL-DIFFERENCES IN THE PREVALENCE OF OPTIC-NERVE GLIOMAS IN NEUROFIBROMATOSIS TYPE, American journal of human genetics, 57(4), 1995, pp. 280-280
MACROCEPHALY IN NEUROFIBROMATOSIS TYPE-1
Authors: COHEN MS SAMANGOSPROUSE CA STERN HJ ROSENBAUM KN TIFFT CJ
Citation: Ms. Cohen et al., MACROCEPHALY IN NEUROFIBROMATOSIS TYPE-1, American journal of human genetics, 57(4), 1995, pp. 465-465
THE NATURAL-HISTORY OF CAFE-AU-LAIT SPOTS IN YOUNG-CHILDREN WITH NEUROFIBROMATOSIS-1
Authors: MCLEAN SD STERN HJ ROSENBAUM KN TIFFT CJ SAAL HM
Citation: Sd. Mclean et al., THE NATURAL-HISTORY OF CAFE-AU-LAIT SPOTS IN YOUNG-CHILDREN WITH NEUROFIBROMATOSIS-1, American journal of human genetics, 53(3), 1993, pp. 474-474
A DE-NOVO PARACENTRIC INVERSION, INV(11)(P13P15.5) IN A CHILD WITH ISOLATED ANIRIDIA
Authors: JOHNSON RC TIFFT CJ STANLEY W
Citation: Rc. Johnson et al., A DE-NOVO PARACENTRIC INVERSION, INV(11)(P13P15.5) IN A CHILD WITH ISOLATED ANIRIDIA, American journal of human genetics, 53(3), 1993, pp. 566-566
Risultati: 1-13 |