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Results: 3

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
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