AAAAAA
Results:
1-16
|
Results: 16
Authors:
PUEL A
MEVEL JC
BOUTHILLIER Y
DECREUSEFOND C
FRIDMAN WH
FEINGOLD N
MOUTON D
Citation: A. Puel et al., IDENTIFICATION OF 2 QUANTITATIVE TRAIT LOCI INVOLVED IN ANTIBODY-PRODUCTION ON MOUSE-CHROMOSOME-8, Immunogenetics, 47(4), 1998, pp. 326-331
Authors:
MERGHOUB T
PERICHON B
MAIERREDELSPERGER M
DIBENEDETTO SP
SAMPERI P
DUCROCQ R
FEINGOLD N
ELION J
SCHILIRO G
LABIE D
KRISHNAMOORTHY R
Citation: T. Merghoub et al., DISSECTION OF THE ASSOCIATION STATUS OF 2 POLYMORPHISMS IN THE BETA-GLOBIN GENE-CLUSTER WITH VARIATIONS IN F-CELL NUMBER IN NONANEMIC INDIVIDUALS, American journal of hematology, 56(4), 1997, pp. 239-243
Authors:
BRIOLLAIS L
CHOMPRET A
GUILLOUDBATAILLE M
FEINGOLD N
AVRIL MF
DEMENAIS F
Citation: L. Briollais et al., GENETIC AND EPIDEMIOLOGIC RISK-FACTORS FOR A MALIGNANT MELANOMA-PREDISPOSING PHENOTYPE - THE GREAT NUMBER OF NEVI, Genetic epidemiology, 13(4), 1996, pp. 385-402
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:
PUEL A
MEVEL JC
BOUTHILLIER Y
FEINGOLD N
FRIDMAN WH
MOUTON D
Citation: A. Puel et al., TOWARD GENETIC DISSECTION OF HIGH AND LOW ANTIBODY RESPONSIVENESS IN BIOZZI MICE, Proceedings of the National Academy of Sciences of the United Statesof America, 93(25), 1996, pp. 14742-14746
Authors:
FARDEAU M
HILLAIRE D
MIGNARD C
FEINGOLD N
FEINGOLD J
MIGNARD D
DEUBEDA B
COLLIN H
TOME FMS
RICHARD I
BECKMANN J
Citation: M. Fardeau et al., JUVENILE LIMB-GIRDLE MUSCULAR-DYSTROPHY CLINICAL, HISTOPATHOLOGICAL AND GENETIC DATA FROM A SMALL COMMUNITY LIVING IN THE REUNION-ISLAND, Brain, 119, 1996, pp. 295-308
Authors:
MERGHOUB T
MAIERREDELSPERGER M
LABIE D
FEINGOLD N
DIBENEDETTO SP
SAMPERI P
SCHILIRO G
DUCROCQ R
ELION J
KRISHNAMOORTHY R
Citation: T. Merghoub et al., VARIATION OF FETAL HEMOGLOBIN AND F-CELL NUMBER WITH THE LCR-HS2 POLYMORPHISM IN NONANEMIC INDIVIDUALS, Blood, 87(6), 1996, pp. 2607-2609
Authors:
KERMARREC N
BLANPIED C
PELLETIER L
FEINGOLD N
MANDET C
DRUET P
HIRSCH F
Citation: N. Kermarrec et al., GENETIC-STUDY OF GOLD-SALT-INDUCED IMMUNE DISORDERS IN THE RAT, Nephrology, dialysis, transplantation, 10(12), 1995, pp. 2187-2191
KERATODERMA WITH SCLEROATROPHY OF THE EXTREMITIES OR SCLEROTYLOSIS (HURIEZ SYNDROME) - A REAPPRAISAL
Authors:
DELAPORTE E
NGUYENMAILFER C
JANIN A
SAVARY JB
VASSEUR F
FEINGOLD N
PIETTE F
BERGOEND H
Citation: E. Delaporte et al., KERATODERMA WITH SCLEROATROPHY OF THE EXTREMITIES OR SCLEROTYLOSIS (HURIEZ SYNDROME) - A REAPPRAISAL, British journal of dermatology, 133(3), 1995, pp. 409-416
Authors:
SAMSON F
MESNARD L
HEIMBURGER M
HANAUER A
CHEVALLAY M
MERCADIER JJ
PELISSIER JF
FEINGOLD N
JUNIEN C
MANDEL JL
FARDEAU M
Citation: F. Samson et al., GENETIC-LINKAGE HETEROGENEITY IN MYOTUBULAR MYOPATHY, American journal of human genetics, 57(1), 1995, pp. 120-126
Authors:
ELBAZ A
VALESANTOS J
JURKATROTT K
LAPIE P
OPHOFF RA
BADY B
LINKS TP
PIUSSAN C
VILA A
MONNIER N
PADBERG GW
ABE K
FEINGOLD N
GUIMARAES J
WINTZEN AR
VANDERHOEVEN JH
SAUDUBRAY JM
GRUNFELD JP
LENOIR G
NIVET H
ECHENNE B
FRANTS RR
FARDEAU M
LEHMANNHORN F
FONTAINE B
Citation: A. Elbaz et al., HYPOKALEMIC PERIODIC PARALYSIS AND THE DIHYDROPYRIDINE RECEPTOR (CACNLIA3) - GENOTYPE-PHENOTYPE CORRELATIONS FOR 2 PREDOMINANT MUTATIONS AND EVIDENCE FOR THE ABSENCE OF A FOUNDER EFFECT IN 16 CAUCASIAN FAMILIES, American journal of human genetics, 56(2), 1995, pp. 374-380
Authors:
HILLAIRE D
LECLERC A
FAURE S
TOPALOGLU H
CHIANNILKULCHAI N
GUICHENEY P
GRINAS L
LEGOS P
PHILPOT J
EVANGELISTA T
ROUTON MC
MAYER M
PELLISSIER JF
ESTOURNET B
BAROIS A
HENTATI F
FEINGOLD N
BECKMANN JS
DUBOWITZ V
TOME FMS
FARDEAU M
Citation: D. Hillaire et al., LOCALIZATION OF MEROSIN-NEGATIVE CONGENITAL MUSCULAR-DYSTROPHY TO CHROMOSOME 6Q2 BY HOMOZYGOSITY MAPPING, Human molecular genetics, 3(9), 1994, pp. 1657-1661
Authors:
FARDEAU M
JACKSON CE
RICHARD H
TISHFIELD J
MIGNARD C
FEINGOLD N
TOME FMS
BECKMANN JS
HILLAIRE D
Citation: M. Fardeau et al., LIMB-GIRDLE MUSCULAR-DYSTROPHY - PHENOTYPIC AND GENOTYPIC COMPARISON BETWEEN AFFECTED FAMILIES IN AMISH AND REUNION-ISLAND COMMUNITIES, Neurology, 44(4), 1994, pp. 10000268-10000269
Authors:
GALACTEROS F
AMAUDRIC F
PREHU C
FEINGOLD N
DOUCETPOPULAIRE F
SOBEL A
ROSA J
Citation: F. Galacteros et al., ACQUIRED UNBALANCED HEMOGLOBIN CHAIN SYNTHESIS DURING HIV-INFECTION, Comptes rendus de l'Academie des sciences. Serie 3, Sciences de la vie, 316(4), 1993, pp. 437-440
Authors:
CASANOVA S
ROSENBERGBOURGIN M
FARKAS D
CALMETTES C
FEINGOLD N
HESHMATI HM
COHEN R
CONTEDEVOLX B
GUILLAUSSEAU PJ
HOUDENT C
BIGORGNE JC
BOITEAU V
CARON J
MODIGLIANI E
Citation: S. Casanova et al., PHEOCHROMOCYTOMA IN MULTIPLE ENDOCRINE NEOPLASIA TYPE-2A - SURVEY OF 100 CASES, Clinical endocrinology, 38(5), 1993, pp. 531-537
Authors:
SAMSON F
HEIMBURGER M
MESNARD L
MERCADIER JJ
HANAUER A
FEINGOLD N
MANDEL JL
FARDEAU M
Citation: F. Samson et al., GENETIC-LINKAGE HETEROGENEITY IN MYOTUBULAR MYOPATHY, American journal of human genetics, 53(3), 1993, pp. 1066-1066
Risultati:
1-16
|