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Authors: KELLY MA JOHNSON P SHAUL M BEALL S CAREY JC
Citation: Ma. Kelly et al., THE COMMUNICATION OF DIFFICULT NEWS TO PARENTS - A PROTOCOL BASED ON PARENT PREFERENCE, Journal of investigative medicine, 46(1), 1998, pp. 100-100

Authors: ROBERTSON J FELDKAMP M JENNINGS J LEENMITCHELL M MARTINEZ L CAREY JC
Citation: J. Robertson et al., MATERNAL ALCOHOL AND CAFFEINE CONSUMPTION AND SPONTANEOUS-ABORTION, Epidemiology, 9(5), 1998, pp. 583-584

Authors: GREALLY MT CAREY JC MILEWICZ DM HUDGINS L GOLDBERG RB SHPRINTZEN RJ COUSINEAU AJ SMITH WL JUDISCH GF HANSON JW
Citation: Mt. Greally et al., SHPRINTZEN-GOLDBERG-SYNDROME - A CLINICAL ANALYSIS, American journal of medical genetics, 76(3), 1998, pp. 202-212

Authors: KRAKOWIAK PA BOHNSACK JF CAREY JC BAMSHAD M
Citation: Pa. Krakowiak et al., CLINICAL ANALYSIS OF A VARIANT OF FREEMAN-SHELDON-SYNDROME (DA2B), American journal of medical genetics, 76(1), 1998, pp. 93-98

Authors: BATTAGLIA A CAREY JC
Citation: A. Battaglia et Jc. Carey, WOLF-HIRSCHHORN-SYNDROME AND PITT-ROGERS-DANKS-SYNDROME, American journal of medical genetics, 75(5), 1998, pp. 541-541

Authors: BAMSHAD M OQUINN JR CAREY JC
Citation: M. Bamshad et al., WOLF-HIRSCHKORN-SYNDROME AND A SPLIT-HAND MALFORMATION, American journal of medical genetics, 75(4), 1998, pp. 351-354

Authors: CAREY JC
Citation: Jc. Carey, NEUROFIBROMATOSIS-NOONAN-SYNDROME, American journal of medical genetics, 75(3), 1998, pp. 263-264

Authors: FLEJTER WL ISSA B SULLIVAN BA CAREY JC BROTHMAN AR
Citation: Wl. Flejter et al., VARIEGATED ANEUPLOIDY IN 2 SIBLINGS - PHENOTYPE, GENOTYPE, CENP-E ANALYSIS, AND LITERATURE-REVIEW, American journal of medical genetics, 75(1), 1998, pp. 45-51

Authors: CAREY JC
Citation: Jc. Carey, BRAVOS OF THE WEST - MYERS,JM, Journal of the West, 37(1), 1998, pp. 100-100

Authors: JOHNSON JP GOLABI M NORTON ME ROSENBLATT RM FELDMAN GM YANG SP HALL BD FRIES MH CAREY JC
Citation: Jp. Johnson et al., COSTELLO-SYNDROME - PHENOTYPE, NATURAL-HISTORY, DIFFERENTIAL-DIAGNOSIS, AND POSSIBLE CAUSE, The Journal of pediatrics, 133(3), 1998, pp. 441-448

Authors: BORGES WG HENSLEY T CAREY JC PETRAK BA HILL HR
Citation: Wg. Borges et al., THE FACE OF JOB, The Journal of pediatrics, 133(2), 1998, pp. 303-305

Authors: FELDMAN GJ WARD DE LAJEUNIERENIER E SAAVEDRA D ROBIN NH PROUD V ROBB LJ KALOUSTIAN VD CAREY JC COHEN MM CORMIER V MUNNICH A ZACKAI EH WILKIE AOM PRICE RA MUENKE M
Citation: Gj. Feldman et al., A NOVEL PHENOTYPIC PATTERN IN X-LINKED INHERITANCE - CRANIOFRONTONASAL SYNDROME MAPS TO XP22, Human molecular genetics, 6(11), 1997, pp. 1937-1941

Authors: TONG KA HARNSBERGER HR DAHLEN RT CAREY JC WARD K
Citation: Ka. Tong et al., LARGE VESTIBULAR AQUEDUCT SYNDROME - A GENETIC-DISEASE, American journal of roentgenology, 168(4), 1997, pp. 1097-1101

Authors: CURRY CJ STEVENSON RE AUGHTON D BYRNE J CAREY JC CASSIDY S CUNNIFF C GRAHAM JM JONES MC KABACK MM MOESCHLER J SCHAEFER GB SCHWARTZ S TARLETON J OPITZ J
Citation: Cj. Curry et al., EVALUATION OF MENTAL-RETARDATION - RECOMMENDATIONS OF A CONSENSUS CONFERENCE, American journal of medical genetics, 72(4), 1997, pp. 468-477

Authors: BLEYL SB MUMFORD BR BROWNHARRISON MC PAGOTTO LT CAREY JC PYSHER TJ WARD K CHIN TK
Citation: Sb. Bleyl et al., XQ28-LINKED NONCOMPACTION OF THE LEFT-VENTRICULAR MYOCARDIUM - PRENATAL-DIAGNOSIS AND PATHOLOGICAL ANALYSIS OF AFFECTED INDIVIDUALS, American journal of medical genetics, 72(3), 1997, pp. 257-265

Authors: CRAVEN CM CAREY JC WARD K
Citation: Cm. Craven et al., UMBILICAL-CORD AGENESIS IN LAMB BODY-WALL DEFECT, American journal of medical genetics, 71(1), 1997, pp. 97-105

Authors: TORIELLO HV CAREY JC SUSLAK E DESPOSITO FR LEONARD B LIPSON M FRIEDMAN BD HOYME HE
Citation: Hv. Toriello et al., 6 PATIENTS WITH ORAL-FACIAL-DIGITAL SYNDROME-IV - THE CASE FOR HETEROGENEITY, American journal of medical genetics, 69(3), 1997, pp. 250-260

Authors: COTCH MF PASTOREK JG NUGENT RP HILLIER SL GIBBS RS MARTIN DH ESCHENBACH DA EDELMAN R CAREY JC REGAN JA KROHN MA KLEBANOFF MA RAO AV RHOADS GG YAFFE SJ CATZ CS MCNELLIS D BERENDES HW BLACKWELDER WC KASLOW RA REED GF GREENBERG EM WILLIAMS S RETTIG PJ
Citation: Mf. Cotch et al., TRICHOMONAS-VAGINALIS ASSOCIATED WITH LOW-BIRTH-WEIGHT AND PRETERM DELIVERY, Sexually transmitted diseases, 24(6), 1997, pp. 353-360

Authors: GUTMANN DH AYLSWORTH A CAREY JC KORF B MARKS J PYERITZ RE RUBENSTEIN A VISKOCHIL D
Citation: Dh. Gutmann et al., THE DIAGNOSTIC EVALUATION AND MULTIDISCIPLINARY MANAGEMENT OF NEUROFIBROMATOSIS-1 AND NEUROFIBROMATOSIS-2, JAMA, the journal of the American Medical Association, 278(1), 1997, pp. 51-57

Authors: HILL HR AUGUSTINE NH ALEXANDER G CAREY JC OCHS HD WEDGWOOD RJ FAVILLE RJ QUIE PG LEPPERT MF
Citation: Hr. Hill et al., FAMILIAL OCCURRENCE OF JOBS SYNDROME OF HYPER-IGE AND RECURRENT INFECTIONS, Journal of allergy and clinical immunology, 99(1), 1997, pp. 1607-1607

Authors: FELDMAN GJ WARD DE ROBIN NH ARONSON AL ZACKAI UH SAAVEDRA D PROUD V ROBB LJ KALOUSTIAN V JABS E CAREY JC MUNNICH A COHEN MM PRICE RA MUENKE M
Citation: Gj. Feldman et al., NOVEL X-LINKED INHERITANCE PATTERN IN CRANIOFRONTONASAL SYNDROME, Journal of dental research, 76, 1997, pp. 3073-3073

Authors: CAREY JC
Citation: Jc. Carey, SETTING THE VIRGIN ON FIRE - CARDENAS,LAZARO, MICHOACAN PEASANTS, ANDTHE REDEMPTION OF THE MEXICAN-REVOLUTION - BECKER,M, The Hispanic American historical review, 77(2), 1997, pp. 327-328

Authors: BATTAGLIA A BIANCHINI E CAREY JC
Citation: A. Battaglia et al., DIAGNOSTIC YIELD OF THE COMPREHENSIVE ASSESSMENT OF DEVELOPMENTAL DELAY IN AN INSTITUTE OF CHILD NEUROPSYCHIATRY, American journal of human genetics, 61(4), 1997, pp. 176-176

Authors: STEVENSON DA BIRCH PH FRIEDMAN JM VISKOCHIL DH CAREY JC
Citation: Da. Stevenson et al., DESCRIPTIVE ANALYSIS OF TIBIAL PSEUDOARTHROSIS IN PATIENTS WITH NEUROFIBROMATOSIS-1, American journal of human genetics, 61(4), 1997, pp. 180-180

Authors: MUENKE M FELDMAN GJ WARD DE LAJEUNIERENIER E SAAVEDRA D ROBIN NH PROUD V ROBB LJ KALOUSTIAN VD CAREY JC COHEN MM CORMIER V MUNNICH A ZACKAI EH WILKIE AOM PRICE RA
Citation: M. Muenke et al., A NOVEL PHENOTYPIC PATTERN IN X-LINKED INHERITANCE - CRANIOFRONTONASAL SYNDROME MAPS TO XP22, American journal of human genetics, 61(4), 1997, pp. 255-255
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