Authors:
MCCONKIEROSELL A
SPIRIDIGLIOZZI GA
IAFOLLA T
TARLETON J
LACHIEWICZ AM
Citation: A. Mcconkierosell et al., CARRIER TESTING IN THE FRAGILE-X-SYNDROME - ATTITUDES AND OPINIONS OFOBLIGATE CARRIERS, American journal of medical genetics, 68(1), 1997, pp. 62-69
Authors:
LACHIEWICZ AM
SPIRIDIGLIOZZI GA
MCCONKIEROSELL A
BURGESS D
FENG Y
WARREN ST
TARLETON J
Citation: Am. Lachiewicz et al., A FRAGILE-X MALE WITH A BROAD SMEAR ON SOUTHERN BLOT ANALYSIS REPRESENTING 100-500 CGG REPEATS AND NO METHYLATION AT THE EAGI SITE OF THE FMR-1 GENE, American journal of medical genetics, 64(2), 1996, pp. 278-282
Authors:
VANHOVE JLK
KISHNANI P
MUENZER J
WENSTRUP RJ
SUMMAR ML
BRUMMOND MR
LACHIEWICZ AM
MILLINGTON DS
KAHLER SG
Citation: Jlk. Vanhove et al., BENZOATE THERAPY AND CARNITINE DEFICIENCY IN NONKETOTIC HYPERGLYCINEMIA, American journal of medical genetics, 59(4), 1995, pp. 444-453
Citation: Dv. Dawson et Am. Lachiewicz, BEHAVIORAL EPIDEMIOLOGY OF FRAGILE-X SYNDROME IN FEMALE PEDIATRIC POPULATIONS, American journal of epidemiology, 141(11), 1995, pp. 50-50
Authors:
LACHIEWICZ AM
SPIRIDIGLIOZZI GA
GULLION CM
RANSFORD SN
RAO K
Citation: Am. Lachiewicz et al., ABERRANT BEHAVIORS OF YOUNG BOYS WITH FRAGILE X-SYNDROME, American journal of mental retardation, 98(5), 1994, pp. 567-579
Authors:
ALBRIGHT SG
LACHIEWICZ AM
TARLETON JC
RAO KW
SCHWARTZ CE
RICHIE R
TENNISON MB
AYLSWORTH AS
Citation: Sg. Albright et al., FRAGILE-X PHENOTYPE IN A PATIENT WITH A LARGE DE-NOVO DELETION IN XQ27-Q28, American journal of medical genetics, 51(4), 1994, pp. 294-297
Citation: Am. Lachiewicz et Dv. Dawson, BEHAVIOR PROBLEMS OF YOUNG GIRLS WITH FRAGILE-X-SYNDROME - FACTOR SCORES ON THE CONNERS PARENTS QUESTIONNAIRE, American journal of medical genetics, 51(4), 1994, pp. 364-369
Citation: Am. Lachiewicz et Dv. Dawson, AUTISTIC BEHAVIORS OF YOUNG GIRLS WITH FRAGILE X-SYNDROME, Pediatric research, 35(4), 1994, pp. 10000023-10000023
Authors:
MCCONKIEROSELL A
LACHIEWICZ AM
SPIRIDIGLIOZZI GA
TARLETON J
SCHOENWALD S
PHELAN MC
GOONEWARDENA P
DING XH
BROWN WT
Citation: A. Mcconkierosell et al., EVIDENCE THAT METHYLATION OF THE FMR-I LOCUS IS RESPONSIBLE FOR VARIABLE PHENOTYPIC-EXPRESSION OF THE FRAGILE-X SYNDROME, American journal of human genetics, 53(4), 1993, pp. 800-809