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Results: 1-25/29
Authors:
PEREIRA E
GOLDBLATT J
RYE P
SANDERSON C
LESOUEF P
Citation: E. Pereira et al., MUTATION ANALYSIS OF INTERLEUKIN-5 IN AN ASTHMATIC COHORT, Human mutation, 11(1), 1998, pp. 51-54
Authors:
PEREIRA E
GOLDBLATT J
RYE P
SANDERSON C
LESOUEF P
Citation: E. Pereira et al., MUTATION ANALYSIS OF INTERLEUKIN-5 IN AN ASTHMATIC COHORT, Human mutation, 11(1), 1998, pp. 51-54
Authors:
GOLDBLATT J
KNOWLES S
Citation: J. Goldblatt et S. Knowles, A UNIQUE LETHAL SPONDYLOCOSTAL METAPHYSEAL DYSPLASIA - A CASE-REPORT, Clinical dysmorphology, 7(2), 1998, pp. 115-118
Authors:
ALBUQUERQUE RV
HAYDEN CM
PALMER LJ
LAING IA
RYE PJ
GIBSON NA
BURTON PR
GOLDBLATT J
LESOUEF PN
Citation: Rv. Albuquerque et al., ASSOCIATION OF POLYMORPHISMS WITHIN THE TUMOR-NECROSIS-FACTOR (TNF) GENES AND CHILDHOOD ASTHMA, Clinical and experimental allergy, 28(5), 1998, pp. 578-584
Authors:
CUMMINS JM
JEQUIER AM
MARTIN R
MEHMET D
GOLDBLATT J
Citation: Jm. Cummins et al., SEMEN LEVELS OF MITOCHONDRIAL-DNA DELETIONS IN MEN ATTENDING AN INFERTILITY CLINIC DO NOT CORRELATE WITH PHENOTYPE, International journal of andrology, 21(1), 1998, pp. 47-52
Authors:
LAING IA
GOLDBLATT J
EBER E
HAYDEN CM
RYE PJ
GIBSON NA
PALMER LJ
BURTON PR
LESOUEF PN
Citation: Ia. Laing et al., A POLYMORPHISM OF THE CC16 GENE IS ASSOCIATED WITH AN INCREASED RISK OF ASTHMA, Journal of Medical Genetics, 35(6), 1998, pp. 463-467
Authors:
CHELI CD
MORRIS DL
KISH L
GOLDBLATT J
NEAMAN I
ALLARD WJ
YEUNG KK
WU AHB
MOORE R
CHAN DW
FRITSCHE HA
SCHWARTZ MK
VERY DL
Citation: Cd. Cheli et al., MULTICENTER EVALUATION OF THE BAYER IMMUNO I(TM) CA 15-3(TM) ASSAY, Clinical chemistry, 44(4), 1998, pp. 765-772
Authors:
WILTON SD
DAVIS M
LIM L
HARKER N
FABIAN V
GOLDBLATT J
LAING NG
Citation: Sd. Wilton et al., AN INTERCHROMOSOMAL DUPLICATION WITHIN THE DYSTROPHIN GENE, Brain pathology, 7(4), 1997, pp. 1118-1118
Authors:
SLEE JJ
WALLMAN IS
GOLDBLATT J
Citation: Jj. Slee et al., A SYNDROME OF LEUKONYCHIA TOTALIS AND MULTIPLE SEBACEOUS CYSTS, Clinical dysmorphology, 6(3), 1997, pp. 229-231
Authors:
WORTHINGTON S
GOLDBLATT J
Citation: S. Worthington et J. Goldblatt, SMITH-LEMLI-OPITZ-SYNDROME - FURTHER DELINEATION OF THE PHENOTYPE, Clinical dysmorphology, 6(3), 1997, pp. 263-266
Authors:
HAYDEN C
PEREIRA E
RYE P
PALMER L
GIBSON N
PALENQUE M
HAGEL I
LYNCH N
GOLDBLATT J
LESOUEF P
Citation: C. Hayden et al., MUTATION SCREENING OF INTERFERON-GAMMA (IFN-GAMMA) AS A CANDIDATE GENE FOR ASTHMA, Clinical and experimental allergy, 27(12), 1997, pp. 1412-1416
Authors:
SINGER SL
WALPOLE I
BROGAN WF
GOLDBLATT J
Citation: Sl. Singer et al., DENTOFACIAL FEATURES OF A FAMILY WITH CROUZON SYNDROME - CASE-REPORTS, Australian dental journal, 42(1), 1997, pp. 11-17
Authors:
WALPOLE IR
WATSON C
MOORE D
GOLDBLATT J
BOWER C
Citation: Ir. Walpole et al., EVALUATION OF A PROJECT TO ENHANCE KNOWLEDGE OF HEREDITARY-DISEASES AND MANAGEMENT, Journal of Medical Genetics, 34(10), 1997, pp. 831-837
Authors:
VERY DL
KISH L
ARRIGO L
NEAMAN I
GOLDBLATT J
MORRIS DL
SORIANO T
AHMED MS
FRITSCHE HA
Citation: Dl. Very et al., VARIABILITY IN THE CONCENTRATION OF PROTEIN PRODUCTS OF THE MUC-1 GENE IN THE SERUM OF NORMAL WOMEN WITH AGE AND MENOPAUSAL STATUS, Clinical chemistry, 43, 1997, pp. 593-593
Authors:
MARTIN RL
WALPOLE I
GOLDBLATT J
Citation: Rl. Martin et al., IDENTIFICATION OF 2 SPORADICALLY DERIVED MUTATIONS IN THE VON HIPPEL-LINDAU GENE, Human mutation, 7(2), 1996, pp. 185-185
Authors:
SLEE J
GOLDBLATT J
Citation: J. Slee et J. Goldblatt, FURTHER EVIDENCE FOR A SYNDROME OF APPLE PEEL INTESTINAL ATRESIA, OCULAR ANOMALIES AND MICROCEPHALY, Clinical genetics, 50(4), 1996, pp. 260-262
Authors:
OLEARY P
BOWER C
MURCH A
CROWHURST J
GOLDBLATT J
Citation: P. Oleary et al., THE IMPACT OF ANTENATAL SCREENING FOR DOWN-SYNDROME IN WESTERN-AUSTRALIA - 1980-1994, Australian and New Zealand Journal of Obstetrics and Gynaecology, 36(4), 1996, pp. 385-388
Authors:
OLEARY PC
NEWNHAM JP
GOLDBLATT J
Citation: Pc. Oleary et al., MEASUREMENT OF FETAL URINARY SODIUM IN OBSTRUCTIVE UROPATHY - A QUESTION OF UNITS, American journal of obstetrics and gynecology, 175(1), 1996, pp. 229-230
Authors:
WALPOLE IR
KOOL DA
EDKINS T
CREEGAN R
LEVITT S
FRANCIS ST
GOLDBLATT J
Citation: Ir. Walpole et al., GENETIC-COUNSELING AND GENE MUTATION ANALYSIS IN FAMILIAL ADENOMATOUSPOLYPOSIS IN WESTERN-AUSTRALIA, Medical journal of Australia, 162(9), 1995, pp. 464-467
Authors:
GOLDBLATT J
CREEGAN R
EDKINS T
LANDAU LI
RYAN G
WALPOLE IR
Citation: J. Goldblatt et al., MUTATION ANALYSIS OF WESTERN-AUSTRALIAN FAMILIES AFFECTED BY CYSTIC-FIBROSIS, Medical journal of Australia, 162(1), 1995, pp. 12-15
Authors:
POULOS A
CHRISTODOULOU J
CHOW CW
GOLDBLATT J
PATON BC
ORII T
SUZUKI Y
SHIMOZAWA N
Citation: A. Poulos et al., PEROXISOMAL ASSEMBLY DEFECTS - CLINICAL, PATHOLOGICAL, AND BIOCHEMICAL FINDINGS IN 2 PATIENTS IN A NEWLY IDENTIFIED COMPLEMENTATION GROUP, The Journal of pediatrics, 127(4), 1995, pp. 596-599
Authors:
GOLDBLATT J
Citation: J. Goldblatt, RADIO SOLUTIONS, Down beat, 62(8), 1995, pp. 8-9
Authors:
SINGER SL
HAAN E
SLEE J
GOLDBLATT J
Citation: Sl. Singer et al., FAMILIAL HEMIFACIAL MICROSOMIA DUE TO AUTOSOMAL-DOMINANT INHERITANCE - CASE-REPORTS, Australian dental journal, 39(5), 1994, pp. 287-291
Authors:
BEILBY J
CHIN CY
PORTER I
WALPOLE IR
GOLDBLATT J
Citation: J. Beilby et al., IMPROVING DIAGNOSIS OF HUNTINGTONS-DISEASE BY ANALYSIS OF AN INTRAGENIC TRINUCLEOTIDE REPEAT EXPANSION, Medical journal of Australia, 161(6), 1994, pp. 356-360
Authors:
WALPOLE IR
PEMBERTON PJ
GOLDBLATT J
BOWER C
Citation: Ir. Walpole et al., SCREENING FOR NEURAL-TUBE DEFECTS, Medical journal of Australia, 160(6), 1994, pp. 384-384