AAAAAA

   
Results: 1-12 |
Results: 12
AUTISM AND MATERNALLY DERIVED ABERRATIONS OF CHROMOSOME 15Q
Authors: SCHROER RJ PHELAN MC MICHAELIS RC CRAWFORD EC SKINNER SA CUCCARO M SIMENSEN RJ BISHOP J SKINNER C FENDER D STEVENSON RE
Citation: Rj. Schroer et al., AUTISM AND MATERNALLY DERIVED ABERRATIONS OF CHROMOSOME 15Q, American journal of medical genetics, 76(4), 1998, pp. 327-336
AUTISM AND MACROCEPHALY
Authors: STEVENSON RE SCHROER RJ SKINNER C FENDER D SIMENSEN RJ
Citation: Re. Stevenson et al., AUTISM AND MACROCEPHALY, Lancet, 349(9067), 1997, pp. 1744-1745
TRINUCLEOTIDE REPEAT EXPANSIONS IN THE FMR1 AND FMR2 GENES ARE NOT COMMON ETIOLOGIC FACTORS IN AUTISTIC-CHILDREN
Authors: LONGSHORE JW TARLETON JC SCHWARTZ CE SKINNER C SKINNER SA SCHROER RJ STEVENSON RE
Citation: Jw. Longshore et al., TRINUCLEOTIDE REPEAT EXPANSIONS IN THE FMR1 AND FMR2 GENES ARE NOT COMMON ETIOLOGIC FACTORS IN AUTISTIC-CHILDREN, American journal of human genetics, 61(4), 1997, pp. 592-592
AN XLMR SYNDROME WITH SHORT STATURE, SMALL HANDS AND FEET, SEIZURES, CLEFT-PALATE, AND GLAUCOMA IS LINKED TO XQ28
Authors: ARMFIELD KB SCHWARTZ CE LUBS HA KRAUSE WL NELSON R HANE B SCHROER RJ ARENA F STEVENSON RE
Citation: Kb. Armfield et al., AN XLMR SYNDROME WITH SHORT STATURE, SMALL HANDS AND FEET, SEIZURES, CLEFT-PALATE, AND GLAUCOMA IS LINKED TO XQ28, American journal of human genetics, 61(4), 1997, pp. 2325-2325
PREVENTABLE FRACTION OF MENTAL-RETARDATION - ANALYSIS BASED ON INDIVIDUALS WITH SEVERE MENTAL-RETARDATION
Authors: STEVENSON RE MASSEY PS SCHROER RJ MCDERMOTT S RICHTER B
Citation: Re. Stevenson et al., PREVENTABLE FRACTION OF MENTAL-RETARDATION - ANALYSIS BASED ON INDIVIDUALS WITH SEVERE MENTAL-RETARDATION, MENTAL RETA, 34(3), 1996, pp. 182-188
NONSYNDROMIC X-LINKED MENTAL-RETARDATION - REVIEW AND MAPPING OF MRX29 TO XP21
Authors: HANE B SCHROER RJ ARENA JF LUBS HA SCHWARTZ CE STEVENSON RE
Citation: B. Hane et al., NONSYNDROMIC X-LINKED MENTAL-RETARDATION - REVIEW AND MAPPING OF MRX29 TO XP21, Clinical genetics, 50(4), 1996, pp. 176-183
CONGENITAL-ANOMALIES IN INDIVIDUALS WITH MENTAL-RETARDATION
Authors: STEVENSON RE SCHROER RJ
Citation: Re. Stevenson et Rj. Schroer, CONGENITAL-ANOMALIES IN INDIVIDUALS WITH MENTAL-RETARDATION, American journal of human genetics, 57(4), 1995, pp. 562-562
INTERSTITIAL DUPLICATION AND TRIPLICATION OF 15Q11-Q13 CONFIRMED BY FLUORESCENCE IN-SITU HYBRIDIZATION
Authors: CRAWFORD EC LETHCO BA BEALER D SCHROER RJ CLARKSON KB PHELAN MC
Citation: Ec. Crawford et al., INTERSTITIAL DUPLICATION AND TRIPLICATION OF 15Q11-Q13 CONFIRMED BY FLUORESCENCE IN-SITU HYBRIDIZATION, American journal of human genetics, 57(4), 1995, pp. 618-618
AARSKOG-SCOTT SYNDROME - CONFIRMATION OF LINKAGE TO THE PERICENTROMERIC REGION OF THE X-CHROMOSOME
Authors: STEVENSON RE MAY M ARENA JF MILLAR EA SCOTT CI SCHROER RJ SIMENSEN RJ LUBS HA SCHWARTZ CE
Citation: Re. Stevenson et al., AARSKOG-SCOTT SYNDROME - CONFIRMATION OF LINKAGE TO THE PERICENTROMERIC REGION OF THE X-CHROMOSOME, American journal of medical genetics, 52(3), 1994, pp. 339-345
LOCALIZATION OF BRANCHIOOTORENAL (BOR) SYNDROME TO A 3 MB REGION OF CHROMOSOME 8Q
Authors: WANG Y TREAT K SCHROER RJ OBRIEN JE STEVENSON RE SCHWARTZ CE
Citation: Y. Wang et al., LOCALIZATION OF BRANCHIOOTORENAL (BOR) SYNDROME TO A 3 MB REGION OF CHROMOSOME 8Q, American journal of medical genetics, 51(2), 1994, pp. 169-175
AARSKOG-SCOTT SYNDROME - LINKAGE ANALYSIS IN THE ORIGINAL SCOTT FAMILY CONFIRMS THE LOCATION OF THE GENE TO XP11.2-]Q12
Authors: SCHWARTZ CE MAY M SCHROER RJ ARENA JF LUBS HA STEVENSON RE
Citation: Ce. Schwartz et al., AARSKOG-SCOTT SYNDROME - LINKAGE ANALYSIS IN THE ORIGINAL SCOTT FAMILY CONFIRMS THE LOCATION OF THE GENE TO XP11.2-]Q12, Cytogenetics and cell genetics, 64(3-4), 1993, pp. 188-188
INVERTED DUPLICATION OF 8P - 10 NEW PATIENTS AND REVIEW OF THE LITERATURE
Authors: FELDMAN GL WEISS L PHELAN MC SCHROER RJ VANDYKE DL
Citation: Gl. Feldman et al., INVERTED DUPLICATION OF 8P - 10 NEW PATIENTS AND REVIEW OF THE LITERATURE, American journal of medical genetics, 47(4), 1993, pp. 482-486
Risultati: 1-12 |