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Citation: Wt. Brown et al., REVERSE MUTATIONS IN THE FRAGILE-X SYNDROME, American journal of medical genetics, 64(2), 1996, pp. 287-292

Authors: BROWN WT NOLIN S HOUCK G DING XH GLICKSMAN A LI SY STARKHOUCK S BROPHY P DUNCAN C DOBKIN C JENKINS E

Citation: Wt. Brown et al., PRENATAL-DIAGNOSIS AND CARRIER SCREENING FOR FRAGILE-X BY PCR, American journal of medical genetics, 64(1), 1996, pp. 191-195

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Citation: N. Zhong et al., FRAGILE-X FOUNDER EFFECTS AND NEW MUTATIONS IN FINLAND, American journal of medical genetics, 64(1), 1996, pp. 226-233

Authors: BROWN WT ZHONG N KAJANOJA E SMITS B CURLEY D WANG D JU W HOUCK G NOLIN S RYYNANEN M

Citation: Wt. Brown et al., FRAGILE-X FOUNDER CHROMOSOME EFFECTS AND NEW MUTATIONS, American journal of human genetics, 57(4), 1995, pp. 913-913

Authors: SHERMAN SL MADDALENA A HOWARDPEEBLES PN BROWN WT NOLIN S JENKINS E SCHWARTZ C TARRELTON J SHAPIRO LR SMITS APT VANOOST BA YOUINGS S JACOBS PA MARTINEZ F BARNICOAT A HOCKEY A STALEY L HAGERMAN R KENNERKNECHT I STEINBACH P BARBI G FILIPPI G GRASSO M TAYLOR SAM ROBINSON H WEBB T BROOME D DIXON J FERREIRA P GUSTAVSON KH MEYER JL PAI GS

Citation: Sl. Sherman et al., CHARACTERISTICS OF THE TRANSMISSION OF THE FMR1 GENE FROM CARRIER FEMALES IN A PROSPECTIVE SAMPLE OF CONCEPTUSES, American journal of medical genetics, 51(4), 1994, pp. 503-506