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Results: 1-25/44
Authors:
KREMER H
CROSBY AH
VANREEN M
KENMOCHI N
ION A
JAMIESON CR
VANDERBURGT I
PATTON MA
MARIMAN ECM
JEFFERY S
Citation: H. Kremer et al., EXCLUSION OF THE MYOSIN LIGHT-CHAIN-2 GENE AND THE RIBOSOMAL-PROTEIN L6 GENE FROM A CAUSATIVE ROLE IN THE PATHOGENESIS OF NOONAN-SYNDROME, European journal of human genetics, 6, 1998, pp. 4184-4184
Authors:
RAJAB A
VAISHNAV A
FREEMAN NV
PATTON MA
Citation: A. Rajab et al., NEURAL-TUBE DEFECTS AND CONGENITAL HYDROCEPHALUS IN THE SULTANATE OF OMAN, Journal of tropical pediatrics, 44(5), 1998, pp. 300-303
Authors:
BRADY AF
PANDYA PP
YUKSEL B
GREENOUGH A
PATTON MA
NICOLAIDES KH
Citation: Af. Brady et al., OUTCOME OF CHROMOSOMALLY NORMAL LIVEBIRTHS WITH INCREASED FETAL NUCHAL TRANSLUCENCY AT 10-14 WEEKS GESTATION, Journal of Medical Genetics, 35(3), 1998, pp. 222-224
Authors:
BRADY AF
JAMIESON CR
VANDERBURGT I
CROSBY A
VANREEN M
KREMER H
MARIMAN E
PATTON MA
JEFFERY S
Citation: Af. Brady et al., FURTHER DELINEATION OF THE CRITICAL REGION FOR NOONAN-SYNDROME ON THELONG ARM OF CHROMOSOME-12, European journal of human genetics, 5(5), 1997, pp. 336-337
Authors:
BRADY AF
PATTON MA
Citation: Af. Brady et Ma. Patton, OSTEOGENESIS IMPERFECTA WITH ARTHROGRYPOSIS MULTIPLEX CONGENITA (BRUCK-SYNDROME) - EVIDENCE FOR POSSIBLE AUTOSOMAL RECESSIVE INHERITANCE, Clinical dysmorphology, 6(4), 1997, pp. 329-336
Authors:
SAGGARMALIK AK
PATTON MA
Citation: Ak. Saggarmalik et Ma. Patton, ORIGINAL CONTRIBUTIONS BY MEDICAL-STUDENTS - INCREASED FEES MAY DISCOURAGE RESEARCH, BMJ. British medical journal, 314(7087), 1997, pp. 1098-1098
Authors:
HATZIPOULIOU A
CHRISTOPOULOU S
JAMIESON CR
TAYLOR JW
MANSOUR S
PATTON MA
Citation: A. Hatzipouliou et al., CYTOGENETIC AND MOLECULAR STUDIES OF 2 PATIENTS WITH AN INTERSTITIAL 9Q DELETION, Cytogenetics and cell genetics, 77(1-2), 1997, pp. 230-230
Authors:
DARYANI YP
BARKER G
PATTON MA
Citation: Yp. Daryani et al., LIMB DEFECTS AS A CONSEQUENCE OF CVS OR UTERINE LAVAGE - A NEED FOR FURTHER DOCUMENTATION OF THE TECHNIQUE AND COMPLICATIONS, Prenatal diagnosis, 17(8), 1997, pp. 789-790
Authors:
DARYANI YP
PENNA LK
PATTON MA
Citation: Yp. Daryani et al., DETECTION OF CELLS OF FETAL ORIGIN FROM TRANSCERVICAL IRRIGATIONS, Prenatal diagnosis, 17(3), 1997, pp. 243-248
Authors:
RAJAB A
PATTON MA
Citation: A. Rajab et Ma. Patton, MAJOR FACTORS DETERMINING THE FREQUENCIES OF HEMOGLOBINOPATHIES IN OMAN, American journal of medical genetics, 71(2), 1997, pp. 240-242
Authors:
RAJAB A
FREEMAN NV
PATTON MA
Citation: A. Rajab et al., HIRSCHSPRUNGS-DISEASE IN OMAN, Journal of pediatric surgery, 32(5), 1997, pp. 724-727
Authors:
MANSOUR S
PATTON MA
Citation: S. Mansour et Ma. Patton, RUSSELL-SILVER-SYNDROME WITH LIMB ABNORMALITIES - 2 CASE-REPORTS, Journal of Medical Genetics, 34, 1997, pp. 538-538
Authors:
ELABD S
WILSON L
HOWLIN P
PATTON MA
WINTGENS AM
WILSON R
Citation: S. Elabd et al., AGENESIS OF THE CORPUS-CALLOSUM IN TURNER SYNDROME WITH RING-X, Developmental Medicine and Child Neurology, 39(2), 1997, pp. 119-124
Authors:
ELABD S
PATTON MA
ABRAMS M
TURK J
REISS A
WARSOFSY I
HOWLIN P
BRITTON J
Citation: S. Elabd et al., PSYCHOLOGICAL FUNCTIONING AND MRI FINDINGS IN RING X TURNER-SYNDROME, American journal of human genetics, 61(4), 1997, pp. 538-538
Authors:
DARYANI YP
BARKER G
PATTON MA
Citation: Yp. Daryani et al., THE RESULTS OF FETAL CELL DETECTION IN THE CERVICAL WASHINGS (CW) IN MORE THAN 100 PREGNANT-WOMEN IN THE FIRST-TRIMESTER OF PREGNANCY, American journal of human genetics, 61(4), 1997, pp. 860-860
Authors:
DADAMO P
FASSONE L
GEDEON A
JANSSEN EAM
BIONE S
BOLHUIS PA
BARTH PG
WILSON M
HAAN E
ORSTAVIK KH
PATTON MA
GREEN AJ
ZAMMARCHI E
DONATI MA
TONIOLO D
Citation: P. Dadamo et al., THE X-LINKED GENE G4.5 IS RESPONSIBLE FOR DIFFERENT INFANTILE DILATEDCARDIOMYOPATHIES, American journal of human genetics, 61(4), 1997, pp. 862-867
Authors:
DOBYNS WB
PATTON MA
STRATTON RF
MASTROBATTISTA JM
BLANTON SH
NORTHRUP H
Citation: Wb. Dobyns et al., COBBLESTONE LISSENCEPHALY WITH NORMAL EYES AND MUSCLE, Neuropediatrics, 27(2), 1996, pp. 70-75
Authors:
BRADY AF
PATTON MA
Citation: Af. Brady et Ma. Patton, WEB-NECK ANOMALY AND ITS ASSOCIATION WITH CONGENITAL HEART-DISEASE, American journal of medical genetics, 64(4), 1996, pp. 605-605
Authors:
SAGGARMALIK AK
PETTITT K
SAGNELLA GA
JEFFERY S
MORGAN S
EASTWOOD JB
PATTON MA
MACGREGOR GA
Citation: Ak. Saggarmalik et al., ADEQUACY OF BLOOD-PRESSURE CONTROL AND RENAL-FUNCTION IN AUTOSOMAL-DOMINANT POLYCYSTIC KIDNEY-DISEASE (APKD), Journal of the American Society of Nephrology, 6(3), 1995, pp. 726-726
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:
GUPTA A
PATTON MA
Citation: A. Gupta et Ma. Patton, FAMILIAL MICROTIA WITH MEATAL ATRESIA AND CONDUCTIVE DEAFNESS IN 5 GENERATIONS, American journal of medical genetics, 59(2), 1995, pp. 238-241
Authors:
WRIGHT AF
BRUFORD EA
THOMSON KL
RIISE R
JAY M
PATTON MA
JEFFERY S
SCHINZEL A
TOMMERUP N
TEAGUE PW
MANSFIELD DC
Citation: Af. Wright et al., GENETIC-LINKAGE ANALYSIS IN 26 FAMILIES WITH BARDET-BIEDL SYNDROME, Investigative ophthalmology & visual science, 36(4), 1995, pp. 774-774
Authors:
JAMIESON CR
VANDERBURG I
WADE AF
VANREEN M
ELSAWI M
HOLS F
JEFFERY S
PATTON MA
MARIMAN E
Citation: Cr. Jamieson et al., MAPPING A GENE FOR NOONAN-SYNDROME TO THE LONG ARM OF CHROMOSOME-12, Journal of Medical Genetics, 32(2), 1995, pp. 143-143
Authors:
SHARLAND M
ELSAWI M
KAMINSKI E
PATTON MA
DAVIES EG
Citation: M. Sharland et al., INCREASED INFECTIONS ASSOCIATED WITH IMMUNOLOGICAL ABNORMALITIES IN NOONAN SYNDROME, Journal of Medical Genetics, 32(2), 1995, pp. 147-147
Authors:
HARRAR H
JEFFREY S
PATTON MA
Citation: H. Harrar et al., LINKAGE STUDIES IN 2 FAMILIES WITH BLEPHAROPHIMOSIS PTOSIS CONFIRMS LINKAGE TO 3Q21-3Q23, Journal of Medical Genetics, 32(2), 1995, pp. 152-152