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Results:
1-16
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Results: 16
Authors:
ANGLE B
BURTON BK
Citation: B. Angle et Bk. Burton, FAMILIAL LEG ULCERS, Lancet, 351(9108), 1998, pp. 1031-1032
Authors:
WANG M
WANG JY
CISLER J
IMAIZUMI K
BURTON BK
JONES MC
LAMBERTI JJ
GODFREY M
Citation: M. Wang et al., 3 NOVEL FIBRILLIN MUTATIONS IN EXON-25 AND EXON-27 - CLASSIC VERSUS NEONATAL MARFAN-SYNDROME, Human mutation, 9(4), 1997, pp. 359-362
Authors:
WEINBERG GL
LAURITO CE
GELDNER P
PYGON BH
BURTON BK
Citation: Gl. Weinberg et al., MALIGNANT VENTRICULAR DYSRHYTHMIAS IN A PATIENT WITH ISOVALERIC ACIDEMIA RECEIVING GENERAL AND LOCAL-ANESTHESIA FOR SUCTION LIPECTOMY, Journal of clinical anesthesia, 9(8), 1997, pp. 668-670
Authors:
DIAZNAZARIO JR
FONTAINE M
MCCORQUODALE DJ
GOULD NS
NIEDERMEYER K
BURTON BK
MCCORQUODALE MM
Citation: Jr. Diaznazario et al., PARTIAL TRISOMY 7Q IN A 22 WEEK FETUS, American journal of human genetics, 61(4), 1997, pp. 692-692
Authors:
SANTOLAYAFORGAS J
JESSUP J
BURD LI
PRINS GS
BURTON BK
Citation: J. Santolayaforgas et al., PREGNANCY OUTCOME IN WOMEN WITH LOW MIDTRIMESTER MATERNAL SERUM UNCONJUGATED ESTRIOL, Journal of reproductive medicine, 41(2), 1996, pp. 87-90
Authors:
ROBIN NH
FELDMAN GJ
ARONSON AL
MITCHELL HF
WEKSBERG R
LEONARD CO
BURTON BK
JOSEPHSON KD
LAXOVA R
ALECK KA
ALLANSON JE
GUIONALMEIDA ML
MARTIN RA
LEICHTMAN LG
PRICE RA
OPITZ JM
MUENKE M
Citation: Nh. Robin et al., OPITZ-SYNDROME IS GENETICALLY HETEROGENEOUS, WITH ONE LOCUS ON XP22, AND A 2ND LOCUS ON 22Q11.2, Nature genetics, 11(4), 1995, pp. 459-461
Authors:
BURTON BK
SCHULZ CJ
ANGLE B
BURD LI
Citation: Bk. Burton et al., AN INCREASED INCIDENCE OF HEMANGIOMAS IN INFANTS BORN FOLLOWING CHORIONIC VILLUS SAMPLING (CVS), Prenatal diagnosis, 15(3), 1995, pp. 209-214
Authors:
NEWLIN AC
MCCORQUODALE MM
MILLER MM
BURTON BK
Citation: Ac. Newlin et al., MOSAIC TRISOMY-7 IN A MALE WITH HYPOMELANOSIS OF ITO AND MULTIPLE CONGENITAL-ANOMALIES, American journal of human genetics, 57(4), 1995, pp. 541-541
Authors:
BRENHOFER JK
BURTON BK
MCCORQUODALE M
Citation: Jk. Brenhofer et al., A CHILD WITH 46,XX,REC(4),DUP P,INV(4) (P15.2Q32) RESULTING FROM A LARGE PATERNAL PERICENTRIC-INVERSION, American journal of human genetics, 57(4), 1995, pp. 604-604
Authors:
SANTOLAYAFORGAS J
BURD LI
BURTON BK
Citation: J. Santolayaforgas et al., CLINICAL-SIGNIFICANCE OF LOW-LEVELS OF 2ND-TRIMESTER MATERNAL SERUM HUMAN CHORIONIC-GONADOTROPIN, Fetal diagnosis and therapy, 9(6), 1994, pp. 362-366
Authors:
GRUBER B
BURTON BK
Citation: B. Gruber et Bk. Burton, OROMANDIBULAR-LIMB HYPOGENESIS SYNDROME FOLLOWING CHORIONIC VILLUS SAMPLING, International journal of pediatric otorhinolaryngology, 29(1), 1994, pp. 59-63
Authors:
ANGLE B
HOLGADO S
BURTON BK
MILLER MT
SHAPIRO MJ
OPITZ JM
Citation: B. Angle et al., MICROCEPHALY, LYMPHEDEMA, AND CHORIORETINAL DYSPLASIA - REPORT OF 2 ADDITIONAL CASES, American journal of medical genetics, 53(2), 1994, pp. 99-101
Authors:
BURTON BK
SCHULZ CJ
BURD LI
Citation: Bk. Burton et al., SPECTRUM OF LIMB DISRUPTION DEFECTS ASSOCIATED WITH CHORIONIC VILLUS SAMPLING, Pediatrics, 91(5), 1993, pp. 989-993
Authors:
BURTON BK
PRINS GS
VERP MS
Citation: Bk. Burton et al., A PROSPECTIVE TRIAL OF PRENATAL SCREENING FOR DOWN-SYNDROME BY MEANS OF MATERNAL SERUM ALPHA-FETOPROTEIN, HUMAN CHORIONIC-GONADOTROPIN, ANDUNCONJUGATED ESTRIOL, American journal of obstetrics and gynecology, 169(3), 1993, pp. 526-530
Authors:
FIELD FM
BURTON BK
Citation: Fm. Field et Bk. Burton, DOMINANTLY INHERITED CLEFT-PALATE, MICROCEPHALY, MENTAL-RETARDATION AND SHORT STATURE, American journal of human genetics, 53(3), 1993, pp. 428-428
Authors:
SANTOLAVAFORGAS J
JESSUP J
KAHN D
PRINS GS
BURTON BK
Citation: J. Santolavaforgas et al., PATIENTS WITH LOW MIDTRIMESTER MATERNAL SERUM UNCONJUGATED ESTRIOL (MSUE3) HAVE AN INCREASED RISK OF PREGNANCY LOSS, American journal of human genetics, 53(3), 1993, pp. 1454-1454
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