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Results:
1-24
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Results: 24
Authors:
GONZALEZ CH
MARQUESDIAS MJ
KIM CA
SUGAYAMA SMM
DAPAZ JA
HUSON SM
HOLMES LB
Citation: Ch. Gonzalez et al., CONGENITAL-ABNORMALITIES IN BRAZILIAN CHILDREN ASSOCIATED WITH MISOPROSTOL MISUSE IN FIRST-TRIMESTER OF PREGNANCY, Lancet, 351(9116), 1998, pp. 1624-1627
Authors:
EVANS DGR
MASON S
HUSON SM
PONDER M
HARDING AE
STRACHAN T
Citation: Dgr. Evans et al., SPINAL AND CUTANEOUS SCHWANNOMATOSIS IS A VARIANT FORM OF TYPE-2 NEUROFIBROMATOSIS - A CLINICAL AND MOLECULAR STUDY, Journal of Neurology, Neurosurgery and Psychiatry, 62(4), 1997, pp. 361-366
Authors:
SLAVOTINEK AM
HUSON SM
FITCHETT M
Citation: Am. Slavotinek et al., INTERSTITIAL DELETION OF BAND 3Q25, Journal of Medical Genetics, 34(5), 1997, pp. 430-432
Authors:
SLAVOTINEK A
MAHER E
GREGORY P
ROWLANDSON P
HUSON SM
Citation: A. Slavotinek et al., THE PHENOTYPIC EFFECTS OF CHROMOSOME REARRANGEMENT INVOLVING BANDS 7Q21.3 AND 22Q13.3, Journal of Medical Genetics, 34(10), 1997, pp. 857-861
Authors:
PIVNICK EK
SHAEFER GB
LIN AE
PARK VM
TOLLEY EA
LAWRENCE MD
HUSON SM
Citation: Ek. Pivnick et al., DELINEATION OF A COMMON FACIAL APPEARANCE IN NEUROFIBROMATOSIS TYPE-1(NF1), American journal of human genetics, 61(4), 1997, pp. 616-616
Authors:
SLAVOTINEK A
HELLEN E
GOULD S
COGHILL SB
HUSON SM
HURST JA
Citation: A. Slavotinek et al., 3 INFANTS OF DIABETIC MOTHERS WITH MALFORMATIONS OF LEFT-RIGHT ASYMMETRY - FURTHER EVIDENCE FOR THE ETIOLOGIC ROLE OF DIABETES IN THIS MALFORMATION SPECTRUM, Clinical dysmorphology, 5(3), 1996, pp. 241-247
Authors:
FIRTH H
BOYD PA
CHAMBERLAIN P
MACKENZIE IZ
HUSON SM
Citation: H. Firth et al., LIMB DEFECTS AND CHORIONIC VILLUS SAMPLING, Lancet, 347(9012), 1996, pp. 1406-1406
Authors:
POULTON J
HUSON SM
Citation: J. Poulton et Sm. Huson, HARDING,ANITA (1952-95) - IN-MEMORIAM, American journal of human genetics, 58(1), 1996, pp. 235-236
Authors:
BARNES PRJ
KANABAR DJ
BRUETON L
NEWSOMDAVIS J
HUSON SM
MANN NP
HILTONJONES D
Citation: Prj. Barnes et al., RECURRENT CONGENITAL ARTHROGRYPOSIS LEADING TO A DIAGNOSIS OF MYASTHENIA-GRAVIS IN AN INITIALLY ASYMPTOMATIC MOTHER, Neuromuscular disorders, 5(1), 1995, pp. 59-65
Authors:
VINCENT A
NEWLAND C
BRUETON L
BEESON D
RIEMERSMA S
HUSON SM
NEWSOMDAVIS J
Citation: A. Vincent et al., ARTHROGRYPOSIS MULTIPLEX CONGENITA WITH MATERNAL AUTOANTIBODIES SPECIFIC FOR A FETAL ANTIGEN, Lancet, 346(8966), 1995, pp. 24-25
Authors:
UPADHYAYA M
MAYNARD J
OSBORN M
HUSON SM
PONDER M
PONDER BAJ
HARPER PS
Citation: M. Upadhyaya et al., CHARACTERIZATION OF GERMLINE MUTATIONS IN THE NEUROFIBROMATOSIS TYPE-1 (NF1) GENE, Journal of Medical Genetics, 32(9), 1995, pp. 706-710
Authors:
ROSSER EM
NORBURY G
GLEW R
JONES L
HUSON SM
Citation: Em. Rosser et al., DIRECT MUTATION ANALYSIS FOR HUNTINGTONS-DISEASE (HD) - THE OXFORD EXPERIENCE, Journal of Medical Genetics, 32(2), 1995, pp. 148-148
Authors:
SLANEY SF
WILKIE AOM
HIRST MC
CHARLTON R
MCKINLEY M
POINTON J
CHRISTODOULOU Z
HUSON SM
DAVIES KE
Citation: Sf. Slaney et al., DNA TESTING FOR FRAGILE-X SYNDROME IN SCHOOLS FOR LEARNING-DIFFICULTIES, Archives of Disease in Childhood, 72(1), 1995, pp. 33-37
Authors:
HUSON SM
Citation: Sm. Huson, WHEN A WOMAN WHO HAS SUFFERED FROM VON RECKLINGHAUSENS DISEASE FOR OVER 20 YEARS WAS PRESCRIBED AMPICILLIN AND FLUCLOXACILLIN HER SKIN SWELLINGS BECAME SMALLER AND SOFTER - WHEN THE DRUG WAS STOPPED THE LUMPS STARTED TO ENLARGE AGAIN - IS THERE ANY EXPLANATION FOR THIS, BMJ. British medical journal, 308(6926), 1994, pp. 468-468
Authors:
FIRTH HV
BOYD P
CHAMBERLAIN P
MACKENZIE I
MORRISSKAY GM
HUSON SM
Citation: Hv. Firth et al., ANALYSIS OF LIMB REDUCTION DEFECTS IN BABIES EXPOSED TO CHRONIC VILLUS SAMPLING, Lancet, 343(8905), 1994, pp. 1069-1071
PRENATAL, PRESYMPTOMATIC, AND DIAGNOSTIC TESTING WITH DIRECT MUTATIONANALYSIS IN HUNTINGTONS-DISEASE
Authors:
ROSSER E
HUSON SM
NORBURY G
Citation: E. Rosser et al., PRENATAL, PRESYMPTOMATIC, AND DIAGNOSTIC TESTING WITH DIRECT MUTATIONANALYSIS IN HUNTINGTONS-DISEASE, Lancet, 343(8895), 1994, pp. 487-488
Authors:
BARNES PRJ
HILTONJONES D
NORBURY G
ROBERTS A
HUSON SM
Citation: Prj. Barnes et al., INCORRECT DIAGNOSIS OF MYOTONIC-DYSTROPHY AND ITS POTENTIAL CONSEQUENCES REVEALED BY SUBSEQUENT DIRECT GENETIC-ANALYSIS, Journal of Neurology, Neurosurgery and Psychiatry, 57(5), 1994, pp. 662-662
Authors:
FEWTRELL MS
TAM PKH
THOMSON AH
FITCHETT M
CURRIE J
HUSON SM
MULLIGAN LM
Citation: Ms. Fewtrell et al., HIRSCHSPRUNGS-DISEASE ASSOCIATED WITH A DELETION OF CHROMOSOME-10 (Q11.2Q21.2) - A FURTHER LINK WITH THE NEUROCRISTOPATHIES, Journal of Medical Genetics, 31(4), 1994, pp. 325-327
Authors:
CHARLTON R
SLANEY S
ROBERTS A
CHEETHAM CM
HUSON SM
SELLER A
Citation: R. Charlton et al., LINKAGE OF A NONSPECIFIC X-LINKED MENTAL-RETARDATION GENE TO XQ26.1, Journal of Medical Genetics, 31(2), 1994, pp. 172-172
Authors:
REARDON W
HALL CM
SLANEY S
HUSON SM
CONNELL J
ALHILALY N
FIXSEN J
BARAITSER M
WINTER RM
Citation: W. Reardon et al., MESOMELIC LIMB SHORTNESS - A PREVIOUSLY UNREPORTED AUTOSOMAL RECESSIVE TYPE, American journal of medical genetics, 47(5), 1993, pp. 788-792
Authors:
WILKIE AOM
CAMPBELL FM
DAUBENEY P
GRANT DB
DANIELS RJ
MULLARKEY M
AFFARA NA
FITCHETT M
HUSON SM
Citation: Aom. Wilkie et al., COMPLETE AND PARTIAL XY SEX REVERSAL ASSOCIATED WITH TERMINAL DELETION OF 10Q - REPORT OF 2 CASES AND LITERATURE-REVIEW, American journal of medical genetics, 46(5), 1993, pp. 597-600
Authors:
SUTHERS GK
DAVIES KE
HUSON SM
Citation: Gk. Suthers et al., MOLECULAR DIAGNOSIS OF MYOTONIC-DYSTROPHY - REPLY, Journal of Medical Genetics, 30(6), 1993, pp. 533-533
Authors:
EVANS DGR
RAMSDEN R
HUSON SM
HARRIS R
LYE R
KING TT
Citation: Dgr. Evans et al., TYPE-2 NEUROFIBROMATOSIS - THE NEED FOR SUPRAREGIONAL CARE, Journal of Laryngology and Otology, 107(5), 1993, pp. 401-406
Authors:
EASTON DF
PONDER MA
HUSON SM
PONDER BAJ
Citation: Df. Easton et al., AN ANALYSIS OF VARIATION IN EXPRESSION OF NEUROFIBROMATOSIS (NF) TYPE-1 (NF1) - EVIDENCE FOR MODIFYING GENES, American journal of human genetics, 53(2), 1993, pp. 305-313
Risultati:
1-24
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