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Results: 1-10 |
Results: 10
ISOLATED HEMIHYPERPLASIA (HEMIHYPERTROPHY) - REPORT OF A PROSPECTIVE MULTICENTER STUDY OF THE INCIDENCE OF NEOPLASIA AND REVIEW
Authors: HOYME HE SEAVER LH JONES KL PROCOPIO F CROOKS W FEINGOLD M
Citation: He. Hoyme et al., ISOLATED HEMIHYPERPLASIA (HEMIHYPERTROPHY) - REPORT OF A PROSPECTIVE MULTICENTER STUDY OF THE INCIDENCE OF NEOPLASIA AND REVIEW, American journal of medical genetics, 79(4), 1998, pp. 274-278
SPONDYLOCARPOTARSAL SYNOSTOSIS SYNDROME IN A 5-YEAR-OLD GIRL AND REVIEW OF 12 CASES
Authors: SEAVER LH BOYD E
Citation: Lh. Seaver et E. Boyd, SPONDYLOCARPOTARSAL SYNOSTOSIS SYNDROME IN A 5-YEAR-OLD GIRL AND REVIEW OF 12 CASES, American journal of human genetics, 61(4), 1997, pp. 633-633
CONGENITAL LYMPHOCYTIC CHORIOMENINGITIS VIRUS-INFECTION
Authors: BARTON LL PETERS CJ SEAVER LH CHARTRAND SA
Citation: Ll. Barton et al., CONGENITAL LYMPHOCYTIC CHORIOMENINGITIS VIRUS-INFECTION, Archives of pediatrics & adolescent medicine, 150(4), 1996, pp. 440-440
A FAMILY WITH UNUSUAL WAARDENBURG SYNDROME TYPE-I (WSI), CLEFT-LIP (PALATE), AND HIRSCHSPRUNG DISEASE IS NOT LINKED TO PAX3
Authors: PIERPONT JW STJACQUES D SEAVER LH ERICKSON RP
Citation: Jw. Pierpont et al., A FAMILY WITH UNUSUAL WAARDENBURG SYNDROME TYPE-I (WSI), CLEFT-LIP (PALATE), AND HIRSCHSPRUNG DISEASE IS NOT LINKED TO PAX3, Clinical genetics, 47(3), 1995, pp. 139-143
FEMALE PSEUDOHERMAPHRODITISM WITH MULTIPLE CAUDAL ANOMALIES - ABSENCEOF Y-SPECIFIC DNA-SEQUENCES AS PATHOGENETIC FACTORS
Authors: SEAVER LH GRIMES J ERICKSON RP
Citation: Lh. Seaver et al., FEMALE PSEUDOHERMAPHRODITISM WITH MULTIPLE CAUDAL ANOMALIES - ABSENCEOF Y-SPECIFIC DNA-SEQUENCES AS PATHOGENETIC FACTORS, American journal of medical genetics, 51(1), 1994, pp. 16-21
FATAL CARDIOMYOPATHY ASSOCIATED WITH 3-HYDROXY-3-METHYLGLUTARYL-COA LYASE DEFICIENCY
Authors: GIBSON KM CASSIDY SB SEAVER LH WANDERS RJA KENNAWAY NG MITCHELL GA SPARK RP
Citation: Km. Gibson et al., FATAL CARDIOMYOPATHY ASSOCIATED WITH 3-HYDROXY-3-METHYLGLUTARYL-COA LYASE DEFICIENCY, Journal of inherited metabolic disease, 17(3), 1994, pp. 291-294
TOLUENE EMBRYOPATHY - DELINEATION OF THE PHENOTYPE AND COMPARISON WITH FETAL ALCOHOL SYNDROME
Authors: PEARSON MA HOYME HE SEAVER LH RIMSZA ME
Citation: Ma. Pearson et al., TOLUENE EMBRYOPATHY - DELINEATION OF THE PHENOTYPE AND COMPARISON WITH FETAL ALCOHOL SYNDROME, Pediatrics, 93(2), 1994, pp. 211-215
PULMONARY ATRESIA ASSOCIATED WITH MATERNAL 22Q11.2 DELETION - POSSIBLE PARENT OF ORIGIN EFFECT IN THE CONOTRUNCAL ANOMALY FACE SYNDROME
Authors: SEAVER LH PIERPONT JW ERICKSON RP DONNERSTEIN RL CASSIDY SB
Citation: Lh. Seaver et al., PULMONARY ATRESIA ASSOCIATED WITH MATERNAL 22Q11.2 DELETION - POSSIBLE PARENT OF ORIGIN EFFECT IN THE CONOTRUNCAL ANOMALY FACE SYNDROME, Journal of Medical Genetics, 31(11), 1994, pp. 830-834
FAMILIAL HYPERPHOSPHATASEMIA - EVIDENCE OF PROGRESSIVE BONY DEFORMITYDESPITE LONG-TERM HUMAN THYROCALCITONIN THERAPY
Authors: HOYME HE SEAVER LH BYERS PH
Citation: He. Hoyme et al., FAMILIAL HYPERPHOSPHATASEMIA - EVIDENCE OF PROGRESSIVE BONY DEFORMITYDESPITE LONG-TERM HUMAN THYROCALCITONIN THERAPY, American journal of human genetics, 53(3), 1993, pp. 452-452
CHROMOSOME 22Q11.2 DELETION IN PATIENTS WITH A NEW FACIAL-CARDIAC SYNDROME
Authors: PIERPONT JW SEAVER LH CASSIDY SB DONNERSTEIN RL ERICKSON RP
Citation: Jw. Pierpont et al., CHROMOSOME 22Q11.2 DELETION IN PATIENTS WITH A NEW FACIAL-CARDIAC SYNDROME, American journal of human genetics, 53(3), 1993, pp. 1212-1212
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