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Results: 1-23 |
Results: 23
SMITH-MAGENIS-SYNDROME
Authors: LACOMBE D MONCLA A MALZAC P MATTEI MG BATTIN J
Citation: D. Lacombe et al., SMITH-MAGENIS-SYNDROME, Archives de pediatrie, 4(5), 1997, pp. 438-442
CHILDRENS HOSPITALS IN BORDEAUX - 3 CENTU RIES OF HISTORY
Authors: BATTIN J
Citation: J. Battin, CHILDRENS HOSPITALS IN BORDEAUX - 3 CENTU RIES OF HISTORY, Archives de pediatrie, 4, 1997, pp. 57-62
OSTEODENSITOMETRY IN TURNER SYNDROME AND GROWTH-HORMONE DEFICIENCY
Authors: BATTIN J BARTHE N BARAT P
Citation: J. Battin et al., OSTEODENSITOMETRY IN TURNER SYNDROME AND GROWTH-HORMONE DEFICIENCY, Archives de pediatrie, 4, 1997, pp. 95-101
PLENARY SESSION - GENES IN DEVELOPMENT AN D ANOMALIES - INTRODUCTION
Authors: STOLL C BATTIN J
Citation: C. Stoll et J. Battin, PLENARY SESSION - GENES IN DEVELOPMENT AN D ANOMALIES - INTRODUCTION, Archives de pediatrie, 4, 1997, pp. 106-106
PARENTAL GENOMIC IMPRINTING AND ITS CONSE QUENCES FOR GROWTH
Authors: BATTIN J
Citation: J. Battin, PARENTAL GENOMIC IMPRINTING AND ITS CONSE QUENCES FOR GROWTH, Archives de pediatrie, 4, 1997, pp. 125-130
18P MONOSOMY WITH MIDLINE DEFECTS AND A DE-NOVO SATELLITE IDENTIFIED BY FISH
Authors: TAINE L GOIZET C WEN ZQ CHATEIL JF BATTIN J SAURA R LACOMBE D
Citation: L. Taine et al., 18P MONOSOMY WITH MIDLINE DEFECTS AND A DE-NOVO SATELLITE IDENTIFIED BY FISH, Annales de genetique, 40(3), 1997, pp. 158-163
A 2ND CHOREA LOCUS ON CHROMOSOME-4
Authors: COUPRY I IMBERT G TAINE L BOISSEAU P BIANCALANA V SAURA R BATTIN J MANDEL JL LACOMBE D ARVEILER B
Citation: I. Coupry et al., A 2ND CHOREA LOCUS ON CHROMOSOME-4, American journal of human genetics, 61(4), 1997, pp. 685-685
ISOLATED MACRODACTYLY AND PROTEUS SYNDROME
Authors: LACOMBE D BATTIN J
Citation: D. Lacombe et J. Battin, ISOLATED MACRODACTYLY AND PROTEUS SYNDROME, Clinical dysmorphology, 5(3), 1996, pp. 255-257
TURNERS-SYNDROME - CURRENT KNOWLEDGE
Authors: BATTIN J
Citation: J. Battin, TURNERS-SYNDROME - CURRENT KNOWLEDGE, Archives de pediatrie, 3(6), 1996, pp. 588-597
X-LINKED DOMINANT CHARCOT-MARIE-TOOTH NEUROPATHY (CMTX) - NEW MUTATIONS IN THE CONNEXIN32 GENE
Authors: RESSOT C LATOUR P BLANQUETGROSSARD F STURTZ F DUTHEL S BATTIN J CORBILLON E OLLAGNON E SERVILLE F VANDENBERGHE A DAUTIGNY A PHAMDINH D
Citation: C. Ressot et al., X-LINKED DOMINANT CHARCOT-MARIE-TOOTH NEUROPATHY (CMTX) - NEW MUTATIONS IN THE CONNEXIN32 GENE, Human genetics, 98(2), 1996, pp. 172-175
DYSMORPHOLOGY AND SYNDROMOLOGY - A JOB FO R GENETIC AND PEDIATRICIAN SPECIALISTS
Authors: BATTIN J LACOMBE D
Citation: J. Battin et D. Lacombe, DYSMORPHOLOGY AND SYNDROMOLOGY - A JOB FO R GENETIC AND PEDIATRICIAN SPECIALISTS, Archives de pediatrie, 2(7), 1995, pp. 615-618
FLOATING-HARBOR SYNDROME - DESCRIPTION OF A FURTHER PATIENT, REVIEW OF THE LITERATURE, AND SUGGESTION OF AUTOSOMAL-DOMINANT INHERITANCE
Authors: LACOMBE D PATTON MA ELLEAU C BATTIN J
Citation: D. Lacombe et al., FLOATING-HARBOR SYNDROME - DESCRIPTION OF A FURTHER PATIENT, REVIEW OF THE LITERATURE, AND SUGGESTION OF AUTOSOMAL-DOMINANT INHERITANCE, European journal of pediatrics, 154(8), 1995, pp. 658-661
FINAL HEIGHT IN TURNER SYNDROME PATIENTS TREATED WITH GROWTH-HORMONE
Authors: ROCHICCIOLI P BATTIN J BERTRAND AM BOST M CABROL S LEBOUC Y CHAUSSAIN JL CHATELAIN P COLLE M CZERNICHOW P DAVID M JOB JC LECORNU M LEHEUP B PIERSON M LIMAL JM MARIANI R PONTE C RAPPAPORT R TAUBER M
Citation: P. Rochiccioli et al., FINAL HEIGHT IN TURNER SYNDROME PATIENTS TREATED WITH GROWTH-HORMONE, Hormone research, 44(4), 1995, pp. 172-176
FINAL HEIGHT OF TURNER SYNDROME CHILDREN AFTER GROWTH-HORMONE TREATMENT
Authors: ROCCHICCIOLI P BATTIN J BERTRAND AM BOST M CABROL S LEBOUC Y CHAUSSAIN JL CHATELAIN P JOB JC LEHEUP B PIERSON M MARIANI R PONTE C RAPPAPORT R
Citation: P. Rocchiccioli et al., FINAL HEIGHT OF TURNER SYNDROME CHILDREN AFTER GROWTH-HORMONE TREATMENT, Archives de pediatrie, 1(4), 1994, pp. 359-362
STUDY OF FINAL HEIGHT IN TURNERS-SYNDROME - ETHNIC AND GENETIC INFLUENCES
Authors: ROCHICCIOLI P DAVID M MALPUECH G COLLE M LIMAL JM BATTIN J MARIANI R SULTAN C NIVELON JL SIMONIN G BOST M CHATELAIN P BERTRAND AM FREYCON R BOUQUIER JJ PIERRON P
Citation: P. Rochiccioli et al., STUDY OF FINAL HEIGHT IN TURNERS-SYNDROME - ETHNIC AND GENETIC INFLUENCES, Acta paediatrica, 83(3), 1994, pp. 305-308
CLINICAL-IDENTIFICATION OF A HUMAN EQUIVALENT TO THE SHORT EAR (SE) MURINE PHENOTYPE
Authors: LACOMBE D TOUTAIN A GORLIN RJ OLEY CA BATTIN J
Citation: D. Lacombe et al., CLINICAL-IDENTIFICATION OF A HUMAN EQUIVALENT TO THE SHORT EAR (SE) MURINE PHENOTYPE, Annales de genetique, 37(4), 1994, pp. 184-191
ADVANCES IN TURNERS-SYNDROME
Authors: BATTIN J
Citation: J. Battin, ADVANCES IN TURNERS-SYNDROME, Contraception fertilite sexualite, 21(12), 1993, pp. 881-885
GERMINAL MOSAICISM IN OCULO-AURICULO-VERTEBRAL DYSPLASIA
Authors: LACOMBE D BATTIN J
Citation: D. Lacombe et J. Battin, GERMINAL MOSAICISM IN OCULO-AURICULO-VERTEBRAL DYSPLASIA, American journal of medical genetics, 46(5), 1993, pp. 609-610
KLINEFELTER SYNDROME IN 1993 - MULTICENTE R STUDY IN 58 PATIENTS AND REVIEW OF THE LITERATURE
Authors: BATTIN J MALPUECH G NIVELON JL GARANDEAU P FREYCON F SULTAN C BOST M SIMONIN G BOUQUIER J ROCHICCIOLI P COLLE M LACOMBE D
Citation: J. Battin et al., KLINEFELTER SYNDROME IN 1993 - MULTICENTE R STUDY IN 58 PATIENTS AND REVIEW OF THE LITERATURE, Annales de pediatrie, 40(7), 1993, pp. 432-437
SPLIT HAND SPLIT FOOT DEFORMITY AND LADD SYNDROME IN A FAMILY - OVERLAP BETWEEN THE EEC AND LADD SYNDROMES
Authors: LACOMBE D SERVILLE F MARCHAND D BATTIN J
Citation: D. Lacombe et al., SPLIT HAND SPLIT FOOT DEFORMITY AND LADD SYNDROME IN A FAMILY - OVERLAP BETWEEN THE EEC AND LADD SYNDROMES, Journal of Medical Genetics, 30(8), 1993, pp. 700-703
COFFIN-LOWRY SYNDROME AND HYPERPROLINEMIA
Authors: LACOMBE D PARROTROULAUD F CASTELL JF SERVILLE F HEHUNSTRE JP BATTIN J
Citation: D. Lacombe et al., COFFIN-LOWRY SYNDROME AND HYPERPROLINEMIA, Archives francaises de pediatrie, 50(6), 1993, pp. 489-492
XY GONADAL-DYSGENESIS AND SRY
Authors: BOUCEKKINE C VILAIN E MCELREAVEY K JAUBERT F BRAUNER R THIBAUD E BATTIN J TOUBLANC JE KUCHERIA K CHAABOUNI S ROBEL P GOMPEL A JOSEPH MG LAMBERT JC LORTATJACOB S NIHOULFEKETE C NIVELON JL SCHAISON G RAPPAPORT R VEKEMANS M VIDEAU M COSTA JM FELLOUS M
Citation: C. Boucekkine et al., XY GONADAL-DYSGENESIS AND SRY, Annales d'Endocrinologie, 54(5), 1993, pp. 315-321
SYNDROMIC FORM OF CONGENITAL CUTIS LAXA
Authors: LACOMBE D FERRANDO MF BIOULAC P SERVILLE F GIMENEZ M LLANAS B DEMARQUEZ JL TAIEB A BATTIN J
Citation: D. Lacombe et al., SYNDROMIC FORM OF CONGENITAL CUTIS LAXA, American journal of human genetics, 53(3), 1993, pp. 1550-1550
Risultati: 1-23 |