AAAAAA

   
Results: 1-11 |
Results: 11
CONGENITAL AUTOSOMAL-DOMINANT DISTAL SPINAL MUSCULAR-ATROPHY
Authors: ADAMS C SUCHOWERSKY O LOWRY RB
Citation: C. Adams et al., CONGENITAL AUTOSOMAL-DOMINANT DISTAL SPINAL MUSCULAR-ATROPHY, Neuromuscular disorders, 8(6), 1998, pp. 405-408
A FURTHER CASE OF HUTTERITE CEREBRO-OSTEO-NEPHRODYSPLASIA
Authors: LOWRY RB
Citation: Rb. Lowry, A FURTHER CASE OF HUTTERITE CEREBRO-OSTEO-NEPHRODYSPLASIA, American journal of medical genetics, 72(4), 1997, pp. 386-386
LOCALIZATION OF THE USHER-SYNDROME TYPE IF (USH1F) TO CHROMOSOME-10
Authors: WAYNE S LOWRY RB MCLEOD DR KNAUS R FARR C SMITH RJH
Citation: S. Wayne et al., LOCALIZATION OF THE USHER-SYNDROME TYPE IF (USH1F) TO CHROMOSOME-10, American journal of human genetics, 61(4), 1997, pp. 1752-1752
MUTATION AND EXPRESSION ANALYSIS OF THE ENDOGLIN GENE IN HEREDITARY HEMORRHAGIC TELANGIECTASIA REVEALS NULL ALLELES - A NEW MODEL FOR PATHOGENESIS
Authors: STENZEL TT GALLIONE CJ KLAUS DJ YEH EY LUX A XUE Y ANTHONY KB MCALLISTER KA BALDWIN MA BERG JN SMITH JD VARY CPH CRAIGEN WJ LOWRY RB WESTERMANN CJJ WARNER ML MILLER YE JACKSON CE GUTTMACHER AE MARCHUK DA
Citation: Tt. Stenzel et al., MUTATION AND EXPRESSION ANALYSIS OF THE ENDOGLIN GENE IN HEREDITARY HEMORRHAGIC TELANGIECTASIA REVEALS NULL ALLELES - A NEW MODEL FOR PATHOGENESIS, American journal of human genetics, 61(4), 1997, pp. 2037-2037
SYNDROME OF MULTIPLE EPIPHYSEAL DYSPLASIA (RIBBING TYPE) WITH RHIZOMELIC SHORTNESS, CLEFT-PALATE, AND MICROGNATHIA IN 2 UNRELATED PATIENTS
Authors: LOWRY RB WESENBERG RL HALL JG
Citation: Rb. Lowry et al., SYNDROME OF MULTIPLE EPIPHYSEAL DYSPLASIA (RIBBING TYPE) WITH RHIZOMELIC SHORTNESS, CLEFT-PALATE, AND MICROGNATHIA IN 2 UNRELATED PATIENTS, American journal of medical genetics, 63(1), 1996, pp. 55-61
SYNTHESIS AND CHARACTERIZATION OF A NOVEL RUTHENIUM ORGANOMETALLIC CIS-[RU(BPY)(2)(NPP)(CL)]CENTER-DOT-BF4 WHERE BPY=2,2'-BIPYRIDYL AND NPP=4-(N-PYRROLYL)PYRIDINE
Authors: ATKINS MJ HARWOOD DJ LOWRY RB
Citation: Mj. Atkins et al., SYNTHESIS AND CHARACTERIZATION OF A NOVEL RUTHENIUM ORGANOMETALLIC CIS-[RU(BPY)(2)(NPP)(CL)]CENTER-DOT-BF4 WHERE BPY=2,2'-BIPYRIDYL AND NPP=4-(N-PYRROLYL)PYRIDINE, Inorganica Chimica Acta, 244(2), 1996, pp. 277-280
ANALYSIS OF SPERM CHROMOSOME COMPLEMENTS FROM A MAN HETEROZYGOUS FOR A PERICENTRIC-INVERSION OF CHROMOSOME-1
Authors: MARTIN RH CHERNOS JE LOWRY RB PATTINSON HA BARCLAY L KO E
Citation: Rh. Martin et al., ANALYSIS OF SPERM CHROMOSOME COMPLEMENTS FROM A MAN HETEROZYGOUS FOR A PERICENTRIC-INVERSION OF CHROMOSOME-1, Human genetics, 93(2), 1994, pp. 135-138
AUTOSOMAL RECESSIVE, FATAL INFANTILE HYPERTONIC MUSCULAR-DYSTROPHY AMONG CANADIAN NATIVES
Authors: LACSON AG SESHIA SS SARNAT HB ANDERSON J DEGROOT WR CHUDLEY A ADAMS C DARWISH HZ LOWRY RB KUHN S LOWRY NJ ANG LC GIBBINGS E TREVENEN CL JOHNSON ES HOOGSTRATEN J
Citation: Ag. Lacson et al., AUTOSOMAL RECESSIVE, FATAL INFANTILE HYPERTONIC MUSCULAR-DYSTROPHY AMONG CANADIAN NATIVES, Canadian journal of neurological sciences, 21(3), 1994, pp. 203-212
X-LINKED RECESSIVE NEPHRITIS WITH MENTAL-RETARDATION, SENSORINEURAL HEARING-LOSS, AND MACROCEPHALY
Authors: ROBSON WLM LOWRY RB LEUNG AKC
Citation: Wlm. Robson et al., X-LINKED RECESSIVE NEPHRITIS WITH MENTAL-RETARDATION, SENSORINEURAL HEARING-LOSS, AND MACROCEPHALY, Clinical genetics, 45(6), 1994, pp. 314-317
FOURIER-TRANSFORM SERS STUDIES OF THE CHEMISORPTION OF FERRICYANIDE ON GOLD ELECTRODE SURFACES
Authors: LOWRY RB
Citation: Rb. Lowry, FOURIER-TRANSFORM SERS STUDIES OF THE CHEMISORPTION OF FERRICYANIDE ON GOLD ELECTRODE SURFACES, Spectrochimica acta. Part A: Molecular spectroscopy, 49(5-6), 1993, pp. 831-836
ABSENT FIBULA AND CRANIOSYNOSTOSIS - A 25-YEAR FOLLOW-UP
Authors: LOWRY RB
Citation: Rb. Lowry, ABSENT FIBULA AND CRANIOSYNOSTOSIS - A 25-YEAR FOLLOW-UP, Journal of Medical Genetics, 30(5), 1993, pp. 445-446
Risultati: 1-11 |