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Results: 26-50/77
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
Authors:
MATHIEU M
PIUSSAN C
THEPOT F
GOUGET A
LACOMBE D
PEDESPAN JM
SERVILLE F
FONTAN D
RUFFIE M
NIVELONCHEVALLIER A
AMBLARD F
CHAUVEAU P
MOIROT H
CHABROLLE JP
CROQUETTE MF
TEYSSIER M
PLAUCHU H
PELISSIER MC
GILGENKRANTZ S
TURCCAREL C
TURLEAU C
PRIEUR M
LEMERRER M
GONZALES M
JOYE N
TAILLEMITE JL
BOUILLIE J
ESCHARD C
MOTTE J
JOURNEL H
Citation: M. Mathieu et al., COLLABORATIVE STUDY OF MOSAIC TETRASOMY 12P OR PALLISTER-KILLIAN-SYNDROME (19 FETUSES OR CHILDREN), Annales de genetique, 40(1), 1997, pp. 45-54
Authors:
LACOMBE D
TAINE L
SAURA R
Citation: D. Lacombe et al., SECKEL-SYNDROME WITH GONADAL-DYSGENESIS, DYSMYELOPOIESIS, RADIAL RAY DEFECT, AND CHROMOSOME INSTABILITY, American journal of human genetics, 61(4), 1997, pp. 583-583
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
Authors:
KARADIMA G
BUGGE M
NICOLAIDIS P
VASSILOPOULOS D
VONBEUST G
PAJARES IL
ALBRECHT B
ANNEREN G
AVRAMOPOULOS D
BLENNOW E
BRONDUMNIELSEN K
CLAUSEN N
GALLAVOUMVOURAKI A
GRIGORIADOU M
HAHNEMANN JM
HERTZ JM
KITSIOUTZELI S
LACOMBE D
MILLER K
MONCLA A
PASSARGE E
PATSALIS PC
PRIEUR M
TSEZOU A
VEKEMANS M
PETERSEN MB
Citation: G. Karadima et al., ORIGIN OF NONDISJUNCTION IN TRISOMY-8 AND TRISOMY-8 MOSAICISM, American journal of human genetics, 61(4), 1997, pp. 732-732
Authors:
VILLARD L
LACOMBE D
FONTES M
Citation: L. Villard et al., A POINT MUTATION IN THE XNP GENE, ASSOCIATED WITH AN ATR-X PHONOTYPE WITHOUT ALPHA-THALASSEMIA, European journal of human genetics, 4(6), 1996, pp. 316-320
Authors:
DEKOK YJM
VOSSENAAR ER
CREMERS CWRJ
DAHL N
LAPORTE J
HU LJ
LACOMBE D
FISCHELGHODSIAN N
FRIEDMAN RA
PARNES LS
THORPE P
BITNERGLINDZICZ M
PANDER HJ
HEILBRONNER H
GRAVELINE J
DENDUNNEN JT
BRUNNER HG
ROPERS HH
CREMERS FPM
Citation: Yjm. Dekok et al., IDENTIFICATION OF A HOT-SPOT FOR MICRODELETIONS IN PATIENTS WITH X-LINKED DEAFNESS TYPE-3 (DFN3) 900 KB PROXIMAL TO THE DFN3 GENE POU3F4, Human molecular genetics, 5(9), 1996, pp. 1229-1235
Authors:
AMIEL J
ATTIE T
JAN D
PELET A
EDERY P
BIDAUD C
LACOMBE D
TAM P
SIMEONI J
FLORI E
NIHOULFEKETE C
MUNNICH A
LYONNET S
Citation: J. Amiel et al., HETEROZYGOUS ENDOTHELIN RECEPTOR-B (EDNRB) MUTATIONS IN ISOLATED HIRSCHSPRUNG DISEASE, Human molecular genetics, 5(3), 1996, pp. 355-357
Authors:
LACOMBE D
BATTIN J
Citation: D. Lacombe et J. Battin, ISOLATED MACRODACTYLY AND PROTEUS SYNDROME, Clinical dysmorphology, 5(3), 1996, pp. 255-257
Authors:
LEVYMOZZICONACCI A
LACOMBE D
LEHEUP B
WERNERT F
ROUAULT F
PHILIP N
Citation: A. Levymozziconacci et al., CHROMOSOME-22Q11 MICRODELETION - A SERIES OF 49 CHILDREN, Archives de pediatrie, 3(8), 1996, pp. 761-768
Authors:
LACOMBE D
Citation: D. Lacombe, CLINICAL DYSMORPHOLOGY AND HUMAN DEVELOPM ENTAL GENES, MS. Medecine sciences, 12(6-7), 1996, pp. 825-830
Authors:
GORRY P
LACOMBE D
CONCORDET JP
Citation: P. Gorry et al., NEVOID BASAL-CELL EPITHELIOMA AND PATCHED - A NEW LINK BETWEEN CANCERAND DEVELOPMENT, MS. Medecine sciences, 12(10), 1996, pp. 1105-1108
Authors:
CZARNECKI P
LACOMBE D
WEISS L
Citation: P. Czarnecki et al., TORIELLO-CAREY SYNDROME - EVIDENCE FOR X-LINKED INHERITANCE, American journal of medical genetics, 65(4), 1996, pp. 291-294
Authors:
TELLIER AL
LYONNET S
CORMIERDAIRE V
DELONLAY P
ABADIE V
BAUMANN C
BONNEAU D
LABRUNE P
LACOMBE D
LEMERRER M
NIVELON A
PHILIP N
BRIARD ML
MUNNICH A
Citation: Al. Tellier et al., INCREASED PATERNAL AGE IN CHARGE ASSOCIATION, Clinical genetics, 50(6), 1996, pp. 548-550
Authors:
LOFFLER P
LACOMBE D
ROSS A
WREDE E
SCHNIEDER L
WELGE KH
Citation: P. Loffler et al., PHOTOFRAGMENT ACTION SPECTROSCOPY OF THE ACETYLENE MOLECULE IN THE VACUUM-ULTRAVIOLET, Chemical physics letters, 252(5-6), 1996, pp. 304-310
Authors:
LACOMBE D
Citation: D. Lacombe, REFORMING FOUCAULT - A CRITIQUE OF THE SOCIAL-CONTROL THESIS, British journal of sociology, 47(2), 1996, pp. 332-352
Authors:
LONGY M
LACOMBE D
Citation: M. Longy et D. Lacombe, COWDEN DISEASE - REPORT A FAMILY AND REVIEW, Annales de genetique, 39(1), 1996, pp. 35-42
Authors:
BIANCALANA V
TAINE L
BOUIX JC
FINCK S
CHAUVIN A
DEVERNEUIL H
KNIGHT SJL
STOLL C
LACOMBE D
MANDEL JL
Citation: V. Biancalana et al., EXPANSION AND METHYLATION STATUS AT FRAXE CAN BE DETECTED ON ECORI BLOTS USED FOR FRAXA DIAGNOSIS - ANALYSIS OF 4 FRAXE FAMILIES WITH MILD MENTAL-RETARDATION IN MALES, American journal of human genetics, 59(4), 1996, pp. 847-854
Authors:
LACOMBE D
Citation: D. Lacombe, ETHICS IN CANCER CLINICAL-TRIALS - A EUROPEAN PERSPECTIVE, European journal of cancer, 31A, 1995, pp. 880-880
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
Authors:
LACOMBE D
ARVEILER B
Citation: D. Lacombe et B. Arveiler, SCHIZOPHRENIA AND DELETIONS IN CHROMOSOME 22Q11, MS. Medecine sciences, 11(12), 1995, pp. 1727-1731
Authors:
BASSE F
LACOMBE D
ABOUSLEIMAN J
PAULY P
DEMARTIN A
Citation: F. Basse et al., BRANCHIOOTORENAL SYNDROME - 4 FAMILIAL CA SES, La Presse medicale, 24(18), 1995, pp. 842-844
Authors:
LACOMBE D
Citation: D. Lacombe, CLINICAL DYSMORPHOLOGY BEYOND DEVELOPMENTAL GENETICS, Collegium antropologicum, 19(2), 1995, pp. 353-363
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
Authors:
LACOMBE D
TAIEB A
Citation: D. Lacombe et A. Taieb, OVERLAP BETWEEN THE BAZEX SYNDROME AND CONGENITAL HYPOTRICHOSIS AND MILIA, American journal of medical genetics, 56(4), 1995, pp. 423-424