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AARSKOG SYNDROME: NEW FINDINGS AND GENETIC ANALYSISESCOBAR V; WEAVER DD.1978; J.A.M.A.; USA; DA. 1978; VOL. 240; NO 24; PP. 2638-2641; BIBL. 13 REF.Article

THE FACIO-GENITO-POPLITEAL SYNDROMEESCOBAR V; WEAVER DD.1978; BIRTH DEFECTS ORIGIN. ARTICLE SER.; USA; DA. 1978; VOL. 14; NO 6B; PP. 185-192; BIBL. 34 REF.Article

A SYNDROME OF MICROCEPHALY, MENTAL RETARDATION, UNUSUAL FACIES, CLEFT PALATE, AND WEIGHT DEFICIENCY.WEAVER DD; WILLIAMS CPS.1977; BIRTH DEFECTS ORIGIN. ARTICLE SER.; U.S.A.; DA. 1977; VOL. 13; NO 3B; PP. 69-84; BIBL. 10 REF.Article

PRENATAL DIAGNOSIS, A COMPILATION OF DIAGNOSED CONDITIONSSTEPHENSON SR; WEAVER DD.1981; AM. J. OBSTET. GYNECOL.; ISSN 0002-9378; USA; DA. 1981; VOL. 141; NO 3; PP. 319-343; BIBL. 301 REF.Article

PERICENTRIC X INVERSION IN DIZYGOTIC TWINS WHO DIFFER IN X CHROMOSOME INACTIVATION AND MENSTRUAL CYCLE FUNCTIONKEITGES EA; PALMER CG; WEAVER DD et al.1982; HUMAN GENETICS; ISSN 0340-6717; DEU; DA. 1982; VOL. 62; NO 3; PP. 210-213; BIBL. 23 REF.Article

THE FETAL TRIMETHADIONE SYNDROME. REPORT OF AN ADDITIONAL FAMILY AND FURTHER DELINEATION OF THIS SYNDROME.FELDMAN GL; WEAVER DD; LOVRIEN EW et al.1977; AMER. J. DIS. CHILD.; U.S.A.; DA. 1977; VOL. 131; NO 12; PP. 1389-1392; BIBL. 31 REF.Article

STUDY OF TWO CASES OF RING 13 CHROMOSOME USING HIGH-RESOLUTION BANDINGJONES IM; PALMER CG; WEAVER DD et al.1981; AM. J. HUM. GENET.; ISSN 0002-9297; USA; DA. 1981; VOL. 33; NO 2; PP. 254-261; BIBL. 27 REF.Article

PRADER-WILLI SYNDROME: ARE THERE POPULATION DIFFERENCES.BUTLER MG; WEAVER DD; MEANEY FJ et al.1982; CLINICAL GENETICS; ISSN 0009-9163; DNK; DA. 1982; VOL. 22; NO 5; PP. 292-294; BIBL. 8 REF.Article

PHENOTYPIC AND GENETIC ANALYSIS OF THE SILVER-RUSSELL SYNDROME.ESCOBAR V; GLEISER S; WEAVER DD et al.1978; CLIN. GENET.; DENM.; DA. 1978; VOL. 13; NO 3; PP. 278-288; BIBL. 2 P.Article

MICROCEPHALY, MICROPHTHALMIA, FALCIFORM RETINAL FOLDS, AND BLINDNESSJARMAS AL; WEAVER DD; ELLIS FD et al.1981; AM. J. DIS. CHILD. (1960); ISSN 0002-922X; USA; DA. 1981; VOL. 135; NO 10; PP. 930-933; BIBL. 21 REF.Article

DICENTRIC CHROMOSOME 13 AND CENTROMERE INACTIVATIONSCHWARTZ S; PALMER CG; WEAVER DD et al.1983; HUMAN GENETICS; ISSN 0340-6717; DEU; DA. 1983; VOL. 63; NO 4; PP. 332-337; BIBL. 1 P.Article

EPIDERMOLYSIS BULLOSA-PYLORIC ATRESIA: AN AUTOSOMAL RECESSIVE SYNDROMEBULL MJ; NORINS AL; WEAVER DD et al.1983; AMERICAN JOURNAL OF DISEASES OF CHILDREN; ISSN 0002-922X; USA; DA. 1983; VOL. 137; NO 5; PP. 449-451; BIBL. 15 REF.Article

CARTILAGE-HAIR HYPOPLASIA, DEFECTIVE T-CELL FUNCTION, AND DIAMOND-BLACKFAN ANEMIA IN AN AMISH CHILDHARRIS RE; BAEHNER RL; GLEISER S et al.1981; AM. J. MED. GENET.; ISSN 0148-7299; USA; DA. 1981; VOL. 8; NO 3; PP. 291-297; BIBL. 23 REF.Article

HYPEREXPLEXIA: AN INHERITED DISORDER OF THE STARTLE RESPONSEMORLEY DJ; WEAVER DD; GARG BP et al.1982; CLINICAL GENETICS; ISSN 0009-9163; DNK; DA. 1982; VOL. 21; NO 6; PP. 388-396; BIBL. 13 REF.Article

FAILURE OF XINACTIVATION IN THE AUTOSOMAL SEGMENT OF AN XIA TRANSLOCATIONPALMER CG; HUBBARD TW; HENRY GW et al.1980; AMER. J. HUM. GENET.; USA; DA. 1980; VOL. 32; NO 2; PP. 179-187; BIBL. 18 REF.Article

JUVENILE CHRONIC GRANULOCYTIC LEUKEMIA IN A PATIENT WITH TRISOMY 8, NEUROFIBROMATOSIS, AND PROLONGED EPSTEIN-BARR VIRUS INFECTIONPALMER CG; PROVISOR AJ; WEAVER DD et al.1983; JOURNAL OF PEDIATRICS; ISSN 0022-3476; USA; DA. 1983; VOL. 102; NO 6; PP. 888-892; BIBL. 16 REF.Article

BRIEF CYTOGENETIC CASE REPORT: A 4.5-YEAR-OLD GIRL WITH DELETION 4Q SYNDROME-DE NOVO, 46,XX,DEL(4) (PTER->Q31:)YOUNG RS; PALMER CG; BENDER HA et al.1982; AM. J. MED. GENET.; ISSN 0148-7299; USA; DA. 1982; VOL. 12; NO 1; PP. 103-107; BIBL. 1 REF.Article

MULTIPLE PTERYGIUM SYNDROMEESCOBAR V; BIXLER D; GLEISER S et al.1978; AMER. J. DIS. CHILD.; USA; DA. 1978; VOL. 132; NO 6; PP. 609-611; BIBL. 20 REF.Article

FEMORAL HYPOPLASIA-UNUSUAL FACIES SYNDROME, FROM ANOTHER VIEWPOINT.GLEISER S; WEAVER DD; ESCOBAR V et al.1978; EUROP. J. PEDIATR.; DEU; DA. 1978; VOL. 128; NO 1; PP. 1-5; BIBL. 15 REF.Article

EVIDENCE FOR TWO ACTIVE X CHROMOSOMES IN A HUMAN XXY TRIPLOID = MISE EN EVIDENCE DE DEUX CHROMOSOMES X ACTIFS DANS UN TRIPLOIDE XXY HUMAINWEAVER DD; GARTER SM; BOUE A et al.1975; HUMANGENETIK; DTSCH.; DA. 1975; VOL. 28; NO 1; PP. 39-42Article

INTERSTITIAL DELETION OF THE LONG ARM OF CHROMOSOME NO 7 (7Q-) IN AN INFANT WITH MULTIPLE ANOMALIES.HIGGINSON G; WEAVER DD; MAGENIS RE et al.1976; CLIN. GENET.; DENM.; DA. 1976; VOL. 10; NO 5; PP. 307-312; BIBL. 1 P.Article

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