AAAAAA

   
Results: 1-10 |
Results: 10
4 CASES OF AMELIA OF THE UPPER-LIMB ASSOCIATED WITH ANAL ATRESIA - ISTHIS VACTERL WITH EXTREME LIMB INVOLVEMENT
Authors: PRICE SM BERRY AC RAYMOND FL TURNPENNY P YOUNG ID
Citation: Sm. Price et al., 4 CASES OF AMELIA OF THE UPPER-LIMB ASSOCIATED WITH ANAL ATRESIA - ISTHIS VACTERL WITH EXTREME LIMB INVOLVEMENT, Clinical dysmorphology, 7(1), 1998, pp. 35-40
NEW THERAPIES FOR CHRONIC OBSTRUCTIVE PULMONARY-DISEASE - COMMENTARY
Authors: RAYMOND FL
Citation: Fl. Raymond, NEW THERAPIES FOR CHRONIC OBSTRUCTIVE PULMONARY-DISEASE - COMMENTARY, Thorax, 53(2), 1998, pp. 148-148
A NEW APPROACH TO THE ELUCIDATION OF COMPLEX CHROMOSOME REARRANGEMENTS ILLUSTRATED BY A CASE OF RIEGER-SYNDROME
Authors: OGILVIE CM RAYMOND FL HARRISON RH SCRIVEN PN DOCHERTY Z
Citation: Cm. Ogilvie et al., A NEW APPROACH TO THE ELUCIDATION OF COMPLEX CHROMOSOME REARRANGEMENTS ILLUSTRATED BY A CASE OF RIEGER-SYNDROME, Journal of Medical Genetics, 35(3), 1998, pp. 234-237
FETAL ECHOCARDIOGRAPHY AS A PREDICTOR OF CHROMOSOMAL ABNORMALITY
Authors: RAYMOND FL SIMPSON JM SHARLAND GK OGILVIE CMM
Citation: Fl. Raymond et al., FETAL ECHOCARDIOGRAPHY AS A PREDICTOR OF CHROMOSOMAL ABNORMALITY, Lancet, 350(9082), 1997, pp. 930-930
PRENATAL-DIAGNOSIS OF 22Q11 DELETIONS - A SERIES OF 5 CASES WITH CONGENITAL HEART-DEFECTS
Authors: RAYMOND FL SIMPSON JM MACKIE CM SHARLAND GK
Citation: Fl. Raymond et al., PRENATAL-DIAGNOSIS OF 22Q11 DELETIONS - A SERIES OF 5 CASES WITH CONGENITAL HEART-DEFECTS, Journal of Medical Genetics, 34(8), 1997, pp. 679-682
SPECTRUM OF CLINICAL-FEATURES ASSOCIATED WITH INTERSTITIAL CHROMOSOME22Q11 DELETIONS - A EUROPEAN COLLABORATIVE STUDY
Authors: RYAN AK GOODSHIP JA WILSON DI PHILIP N LEVY A SEIDEL H SCHUFFENHAUER S OECHSLER H BELOHRADSKY B PRIEUR M AURIAS A RAYMOND FL CLAYTONSMITH J HATCHWELL E MCKEOWN C BEEMER FA DALLAPICCOLA B NOVELLI G HURST JA IGNATIUS J GREEN AJ WINTER RM BRUETON L BRONDUMNIELSEN K STEWART F VANESSEN T PATTON M PATERSON J SCAMBLER PJ
Citation: Ak. Ryan et al., SPECTRUM OF CLINICAL-FEATURES ASSOCIATED WITH INTERSTITIAL CHROMOSOME22Q11 DELETIONS - A EUROPEAN COLLABORATIVE STUDY, Journal of Medical Genetics, 34(10), 1997, pp. 798-804
MYOTONIC-DYSTROPHY PRESENTING WITH A SEVERE SENSORY AND MOTOR NEUROPATHY
Authors: RAYMOND FL MALE AM ROBB S HADDEN RDM HUGHES RAC
Citation: Fl. Raymond et al., MYOTONIC-DYSTROPHY PRESENTING WITH A SEVERE SENSORY AND MOTOR NEUROPATHY, Journal of Medical Genetics, 34, 1997, pp. 524-524
LOCALIZATION OF THE FAMILIAL SHORT STATURE GENE ON XP22.3
Authors: RAYMOND FL ROSS BJ MACKIEOGILVIE CM
Citation: Fl. Raymond et al., LOCALIZATION OF THE FAMILIAL SHORT STATURE GENE ON XP22.3, Journal of Medical Genetics, 34, 1997, pp. 1205-1205
SPINAL MUSCULAR-ATROPHY OF CHILDHOOD - GENETICS
Authors: RAYMOND FL
Citation: Fl. Raymond, SPINAL MUSCULAR-ATROPHY OF CHILDHOOD - GENETICS, Developmental Medicine and Child Neurology, 39(6), 1997, pp. 419-420
ISOMERISM OF THE ATRIAL APPENDAGES ASSOCIATED WITH 22Q11 DELETION IN A FETUS
Authors: YATES RWM RAYMOND FL COOK A SHARLAND GK
Citation: Rwm. Yates et al., ISOMERISM OF THE ATRIAL APPENDAGES ASSOCIATED WITH 22Q11 DELETION IN A FETUS, HEART, 76(6), 1996, pp. 548-549
Risultati: 1-10 |