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Results:
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Results: 13
Authors:
BURLET P
HUBER C
BERTRANDY S
LUDOSKY MA
ZWAENEPOEL I
CLERMONT O
ROUME J
DELEZOIDE AL
CARTAUD J
MUNNICH A
LEFEBVRE S
Citation: P. Burlet et al., THE DISTRIBUTION OF SMN PROTEIN COMPLEX IN HUMAN FETAL TISSUES AND ITS ALTERATION IN SPINAL MUSCULAR-ATROPHY, Human molecular genetics (Print), 7(12), 1998, pp. 1927-1933
Authors:
JOBERT AS
ZHANG P
COUVINEAU A
BONAVENTURE J
ROUME J
LEMERRER M
SILVE C
Citation: As. Jobert et al., ABSENCE OF FUNCTIONAL RECEPTORS FOR PARATHYROID-HORMONE AND PARATHYROID HORMONE-RELATED PEPTIDE IN BLOMSTRAND CHONDRODYSPLASIA, The Journal of clinical investigation, 102(1), 1998, pp. 34-40
Authors:
ROUME J
GENIN E
CORMIERDAIRE V
MA HW
MEHAYE B
ATTIE T
RAZAVIENCHA F
FALLETBIANCO C
BUENERD A
CLERGETDARPOUX F
MUNNICH A
LEMERRER M
Citation: J. Roume et al., A GENE FOR MECKEL SYNDROME MAPS TO CHROMOSOME 11Q13, American journal of human genetics, 63(4), 1998, pp. 1095-1101
Authors:
ROUME J
GONZALES M
MULLIEZ N
Citation: J. Roume et al., THE PATHOLOGIST IN PRENATAL-DIAGNOSIS AND GENETIC-COUNSELING, Annales de pathologie, 17(4), 1997, pp. 236-239
Authors:
LABRUNE P
TRIOCHE P
FALLETBIANCO C
ROUME J
NARCY F
LEMERRER M
Citation: P. Labrune et al., SEVERE BRAIN AND LIMB DEFECTS WITH POSSIBLE AUTOSOMAL RECESSIVE INHERITANCE - A SERIES OF 6 CASES AND REVIEW OF THE LITERATURE, American journal of medical genetics, 73(2), 1997, pp. 144-149
Authors:
LOSHKAJIAN A
ROUME J
STANESCU V
DELEZOIDE AL
STAMPF F
MAROTEAUX P
Citation: A. Loshkajian et al., FAMILIAL BLOMSTRAND CHONDRODYSPLASIA WITH ADVANCED SKELETAL MATURATION - FURTHER DELINEATION, American journal of medical genetics, 71(3), 1997, pp. 283-288
EXCESSIVE SPINAL CELL-DEATH IS RESPONSIBLE FOR NEURONAL DEPLETION IN TYPE-III LISSENCEPHALY SYNDROME
Authors:
ENCHARAZAVI F
MARTINOVIC Y
PORON F
MULLIEZ N
ROUME J
GONZALES M
LARROCHE JC
Citation: F. Encharazavi et al., EXCESSIVE SPINAL CELL-DEATH IS RESPONSIBLE FOR NEURONAL DEPLETION IN TYPE-III LISSENCEPHALY SYNDROME, Journal of neuropathology and experimental neurology, 56(5), 1997, pp. 127-127
Authors:
ROUME J
MA HW
LEMERRER M
CORMIERDAIRE V
GIRLICH D
GENIN E
MUNNICH A
Citation: J. Roume et al., GENETIC-HETEROGENEITY OF MECKEL-SYNDROME, Journal of Medical Genetics, 34(12), 1997, pp. 1003-1006
Authors:
RAZAVI FE
LARROCHE JC
ROUME J
GONZALES M
KONDO HC
MULLIEZ N
Citation: Fe. Razavi et al., LETHAL FAMILIAL FETAL AKINESIA SEQUENCE (FAS) WITH DISTINCT NEUROPATHOLOGICAL PATTERN - TYPE-III LISSENCEPHALY SYNDROME, American journal of medical genetics, 62(1), 1996, pp. 16-22
Authors:
DAMSIN JP
ZAMBELLI JY
MA R
ROUME J
COLONNA F
HANNOUN L
Citation: Jp. Damsin et al., STUDY OF THE ARTERIAL VASCULARIZATION OF THE MEDIAL TIBIAL CONDYLE INTHE FETUS, Surgical and radiologic anatomy, 17(1), 1995, pp. 13-17
Authors:
BROSSARD Y
AUBIN JT
MANDELBROT L
BIGNOZZI C
BRAND D
CHAPUT A
ROUME J
MULLIEZ N
MALLET F
AGUT H
BARIN F
BRECHOT C
GOUDEAU A
HURAUX JM
BARRAT J
BLOT P
CHAVINIE J
CIRARUVIGNERON N
ENGELMAN P
HERVE F
PAPIERNIK E
HENRION R
Citation: Y. Brossard et al., FREQUENCY OF EARLY IN-UTERO HIV-1 INFECTION - A BLIND DNA-POLYMERASE CHAIN-REACTION STUDY ON 100 FETAL THYMUSES, AIDS, 9(4), 1995, pp. 359-366
Authors:
SIFFROI JP
GOMES DM
ROUME J
Citation: Jp. Siffroi et al., THE FETAL PHENOTYPE OF PARTIAL 2Q TRISOMY, Prenatal diagnosis, 15(4), 1995, pp. 382-384
Authors:
ENCHARAZAVI F
ROUME J
KONDO H
GONZALES M
MULLIEZ N
LARROCHE JC
Citation: F. Encharazavi et al., NEUROPATHOLOGICAL CHANGES DISTINCTIVE OF A FAMILIAL FORM OF FETAL AKINESIA SEQUENCE (FAS) - PATHOGENETIC CONSIDERATIONS, Journal of neuropathology and experimental neurology, 54(3), 1995, pp. 469-469
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