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Results: 1-25 | 26-30 |
Results: 26-30/30
APPARENT GENETIC HOMOGENEITY OF THE TREACHER COLLINS-FRANCESCHETTI SYNDROME
Authors: EDERY P MANACH Y LEMERRER M TILL M VIGNAL A LYONNET S MUNNICH A
Citation: P. Edery et al., APPARENT GENETIC HOMOGENEITY OF THE TREACHER COLLINS-FRANCESCHETTI SYNDROME, American journal of medical genetics, 52(2), 1994, pp. 174-177
MUTATIONS OF THE RET PROTOONCOGENE IN HIRSCHSPRUNGS-DISEASE
Authors: EDERY P LYONNET S MULLIGAN LM PELET A DOW E ABEL L HOLDER S NIHOULFEKETE C PONDER BAJ MUNNICH A
Citation: P. Edery et al., MUTATIONS OF THE RET PROTOONCOGENE IN HIRSCHSPRUNGS-DISEASE, Nature, 367(6461), 1994, pp. 378-380
LONG-SEGMENT AND SHORT SEGMENT FAMILIAL HIRSCHSPRUNGS-DISEASE - VARIABLE CLINICAL EXPRESSION AT THE RET LOCUS
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
MUSCLE ADENOSINE-MONOPHOSPHATE DEAMINASE DEFICIENCY (AMPD1)
Authors: BELDJORD C BORNENS M BURSAUX E DREYFUS JC EDERY P FISCHER A GILGENKRANTZ H GRUNFELD JP KAHN A LABIE D LOTTEAU V LYONNET S MUNNICH A NIHOULFEKETE C DEROUFFIGNAC C
Citation: C. Beldjord et al., MUSCLE ADENOSINE-MONOPHOSPHATE DEAMINASE DEFICIENCY (AMPD1), MS. Medecine sciences, 9(8-9), 1993, pp. 983-984
HIRSCHSPRUNG DISEASE - MAPPING OF A DOMINANT GENE CLOSELY LINKED TO THE RET LOCUS ON THE PROXIMAL LONG ARM OF CHROMOSOME-10
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
Risultati: 1-25 | 26-30 |