Authors:
CASSIDY SB
FORSYTHE M
HEEGER S
NICHOLLS RD
SCHORK N
BENN P
SCHWARTZ S
Citation: Sb. Cassidy et al., COMPARISON OF PHENOTYPE BETWEEN PATIENTS WITH PRADER-WILLI-SYNDROME DUE TO DELETION 15Q AND UNIPARENTAL DISOMY-15, American journal of medical genetics, 68(4), 1997, pp. 433-440
Citation: P. Benn, AGING CHROMOSOME TELOMERES - PARALLEL STUDIES WITH TERMINAL REPEAT AND TELOMERE-ASSOCIATED DNA PROBES, Mechanism of ageing and development, 99(2), 1997, pp. 153-166
Authors:
CANAVERO S
BONICALZI V
FERROLI P
ZEME S
MONTALENTI E
BENN P
Citation: S. Canavero et al., LAMOTRIGINE CONTROL OF IDIOPATHIC TRIGEMINAL NEURALGIA, Journal of Neurology, Neurosurgery and Psychiatry, 59(6), 1995, pp. 646-646
Authors:
BENN P
CRAFFEY A
HORNE D
CUSICK W
SMELTZER J
Citation: P. Benn et al., AN ASSOCIATION BETWEEN TRISOMY-16 (AND OTHER FETAL ANEUPLOIDY) IN WOMEN WITH GROSSLY ELEVATED 2ND-TRIMESTER MATERNAL SERUM HUMAN CHORIONIC-GONADOTROPIN (MSHCG), American journal of human genetics, 57(4), 1995, pp. 1597-1597
Authors:
DEVI AS
VELINOV M
KAMATH MV
EISENFELD L
NEU R
CIARLEGLIO L
GREENSTEIN R
BENN P
Citation: As. Devi et al., VARIABLE CLINICAL EXPRESSION OF MOSAIC TRISOMY-16 IN THE NEWBORN-INFANT, American journal of medical genetics, 47(2), 1993, pp. 294-298