Authors:
BAHUAU M
FLINTOFF W
ASSOULINE B
LYONNET S
LEMERRER M
PRIEUR M
GUILLOUDBATAILLE M
FEINGOLD N
MUNNICH A
VIDAUD M
VIDAUD D
Citation: M. Bahuau et al., EXCLUSION OF ALLELISM OF NOONAN-SYNDROME AND NEUROFIBROMATOSIS-TYPE-1IN A LARGE FAMILY WITH NOONAN-SYNDROME NEUROFIBROMATOSIS ASSOCIATION, American journal of medical genetics, 66(3), 1996, pp. 347-355
Authors:
EDERY P
PELET A
MULLIGAN LM
ABEL L
ATTIE T
DOW E
BONNEAU D
DAVID A
FLINTOFF W
JAN D
JOURNEL H
LACOMBE D
LEMERRER M
MEIJERS C
PARENT P
PHILIP N
PLAUCHU H
SARDA P
VERLOES A
NIHOULFEKETE C
WILLIAMSON R
PONDER BAJ
MUNNICH A
LYONNET S
Citation: P. Edery et al., LONG-SEGMENT AND SHORT SEGMENT FAMILIAL HIRSCHSPRUNGS-DISEASE - VARIABLE CLINICAL EXPRESSION AT THE RET LOCUS, Journal of Medical Genetics, 31(8), 1994, pp. 602-606
Authors:
EDERY P
LYONNET S
ABEL L
LEMERRER M
PELET A
FLINTOFF W
NIHOULFEKETE C
WEISSENBACH J
MUNNICH A
Citation: P. Edery et al., HIRSCHSPRUNG DISEASE - MAPPING OF A DOMINANT GENE CLOSELY LINKED TO THE RET LOCUS ON THE PROXIMAL LONG ARM OF CHROMOSOME-10, American journal of human genetics, 53(3), 1993, pp. 996-996