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Results: 1-14 |
Results: 14
TESTING FOR INTERACTION BETWEEN MATERNAL SMOKING AND TGFA GENOTYPE AMONG ORAL CLEFT CASES BORN IN MARYLAND 1992-1996
Authors: BEATY TH MAESTRI NE HETMANSKI JB WYSZYNSKI DF VANDERKOLK CA SIMPSON JC MCINTOSH I SMITH EA ZEIGER JS RAYMOND GV PANNY SR TIFFT CJ LEWANDA AF CRISTION CA WULFSBERG EA
Citation: Th. Beaty et al., TESTING FOR INTERACTION BETWEEN MATERNAL SMOKING AND TGFA GENOTYPE AMONG ORAL CLEFT CASES BORN IN MARYLAND 1992-1996, The Cleft palate-craniofacial journal, 34(5), 1997, pp. 447-454
EVIDENCE FOR AN ASSOCIATION BETWEEN MARKERS ON CHROMOSOME 19Q AND NON-SYNDROMIC CLEFT-LIP WITH OR WITHOUT DEFT PALATE IN 2 GROUPS OF MULTIPLEX FAMILIES
Authors: WYSZYNSKI DF MAESTRI N MCINTOSH I SMITH EA LEWANDA AF GARCIADELGADO C VINAGERASGUARNEROS E WULFSBERG E BEATY TH
Citation: Df. Wyszynski et al., EVIDENCE FOR AN ASSOCIATION BETWEEN MARKERS ON CHROMOSOME 19Q AND NON-SYNDROMIC CLEFT-LIP WITH OR WITHOUT DEFT PALATE IN 2 GROUPS OF MULTIPLEX FAMILIES, Human genetics, 99(1), 1997, pp. 22-26
PARTIAL TRISOMY 10P FROM MATERNAL PERICENTRIC-INVERSION WITH SEVERE NEUROLOGIC SEQUELAE
Authors: ANIKSTER Y GROPMAN A LEWANDA AF TIFFT C SCHONBERG S KRASNEWICH D
Citation: Y. Anikster et al., PARTIAL TRISOMY 10P FROM MATERNAL PERICENTRIC-INVERSION WITH SEVERE NEUROLOGIC SEQUELAE, American journal of human genetics, 61(4), 1997, pp. 500-500
MUTATIONAL ANALYSIS OF FGFR3 IN THANATOPHORIC DYSPLASIA, TYPE-I
Authors: BELLUS GA BAKER A SPECTOR EB HUNTER AGW HECHT J LEWANDA AF SZABO J FRANCOMANO CA
Citation: Ga. Bellus et al., MUTATIONAL ANALYSIS OF FGFR3 IN THANATOPHORIC DYSPLASIA, TYPE-I, American journal of human genetics, 61(4), 1997, pp. 1908-1908
DEFORMATIONS IN INFANTS BORN TO MOTHERS WITH UTERINE MALFORMATIONS - REPORT OF 4 NEW CASES
Authors: LEWANDA AF
Citation: Af. Lewanda, DEFORMATIONS IN INFANTS BORN TO MOTHERS WITH UTERINE MALFORMATIONS - REPORT OF 4 NEW CASES, American journal of human genetics, 61(4), 1997, pp. 2159-2159
NO EVIDENCE OF LINKAGE FOR CLEFT-LIP WITH OR WITHOUT CLEFT-PALATE TO A MARKER NEAR THE TRANSFORMING GROWTH-FACTOR-ALPHA LOCUS IN 2 POPULATIONS
Authors: WYSZYNSKI DF MAESTRI N LEWANDA AF MCINTOSH I SMITH EA GARCIADELGADO C VINAGERASGUARNEROS E WULFSBERG E BEATY TH
Citation: Df. Wyszynski et al., NO EVIDENCE OF LINKAGE FOR CLEFT-LIP WITH OR WITHOUT CLEFT-PALATE TO A MARKER NEAR THE TRANSFORMING GROWTH-FACTOR-ALPHA LOCUS IN 2 POPULATIONS, Human heredity, 47(2), 1997, pp. 101-109
CRANIOSYNOSTOSIS AND SKELETAL DYSPLASIAS - FIBROBLAST GROWTH-FACTOR RECEPTOR DEFECTS
Authors: LEWANDA AF MEYER GA JABS EW
Citation: Af. Lewanda et al., CRANIOSYNOSTOSIS AND SKELETAL DYSPLASIAS - FIBROBLAST GROWTH-FACTOR RECEPTOR DEFECTS, Proceedings of the Association of American Physicians, 108(1), 1996, pp. 19-24
PHENOTYPIC DISCORDANCE IN A FAMILY WITH MONOZYGOTIC TWINS AND NON-SYNDROMIC CLEFT-LIP AND PALATE
Authors: WYSZYNSKI DF LEWANDA AF BEATY TH
Citation: Df. Wyszynski et al., PHENOTYPIC DISCORDANCE IN A FAMILY WITH MONOZYGOTIC TWINS AND NON-SYNDROMIC CLEFT-LIP AND PALATE, American journal of medical genetics, 66(4), 1996, pp. 468-470
2 CRANIOSYNOSTOTIC PATIENTS WITH 11Q DELETIONS, AND REVIEW OF 48 CASES
Authors: LEWANDA AF MORSEY S REID CS JABS EW
Citation: Af. Lewanda et al., 2 CRANIOSYNOSTOTIC PATIENTS WITH 11Q DELETIONS, AND REVIEW OF 48 CASES, American journal of medical genetics, 59(2), 1995, pp. 193-198
MOLECULAR CYTOGENETIC ANALYSIS OF CHROMOSOME 7P ANOMALIES AND CLINICAL CORRELATION WITH SAETHRE-CHOTZEN SYNDROME
Authors: GOODMAN BK GREEN ED LEWANDA AF ROSENGREN S JABS EW
Citation: Bk. Goodman et al., MOLECULAR CYTOGENETIC ANALYSIS OF CHROMOSOME 7P ANOMALIES AND CLINICAL CORRELATION WITH SAETHRE-CHOTZEN SYNDROME, American journal of human genetics, 57(4), 1995, pp. 636-636
2 CRANIOSYNOSTOTIC SYNDROME LOCI, CROUZON AND JACKSON-WEISS, MAP TO CHROMOSOME-10Q23-Q26
Authors: LI XA LEWANDA AF ELUMA F JERALD H CHOI H ALOZIE I PROUKAKIS C TALBOT CC VANDERKOLK C BIRD LM JONES MC CUNNINGHAM M CLARREN SK PYERITZ RE WEISSENBACH J JACKSON CE JABS EW
Citation: Xa. Li et al., 2 CRANIOSYNOSTOTIC SYNDROME LOCI, CROUZON AND JACKSON-WEISS, MAP TO CHROMOSOME-10Q23-Q26, Genomics, 22(2), 1994, pp. 418-424
GENETIC-HETEROGENEITY AMONG CRANIOSYNOSTOSIS SYNDROMES - MAPPING THE SAETHRE-CHOTZEN SYNDROME LOCUS BETWEEN D7S513 AND D7S516 AND EXCLUSIONOF JACKSON-WEISS AND CROUZON SYNDROME LOCI FROM 7P
Authors: LEWANDA AF COHEN MM JACKSON CE TAYLOR EW LI X BELOFF M DAY D CLARREN SK ORTIZ R GARCIA C HAUSELMAN E FIGUEROA A WULFSBERG E WILSON M WARMAN ML PADWA BL WHITEMAN DAH MULLIKEN JB JABS EW
Citation: Af. Lewanda et al., GENETIC-HETEROGENEITY AMONG CRANIOSYNOSTOSIS SYNDROMES - MAPPING THE SAETHRE-CHOTZEN SYNDROME LOCUS BETWEEN D7S513 AND D7S516 AND EXCLUSIONOF JACKSON-WEISS AND CROUZON SYNDROME LOCI FROM 7P, Genomics, 19(1), 1994, pp. 115-119
EVIDENCE THAT THE SAETHRE-CHOTZEN SYNDROME LOCUS LIES BETWEEN D7S664 AND D7S507, BY GENETIC-ANALYSIS AND DETECTION OF A MICRODELETION IN A PATIENT
Authors: LEWANDA AF GREEN ED WEISSENBACH J JERALD H TAYLOR E SUMMAR ML PHILLIPS JA COHEN M FEINGOLD M MOURADIAN W CLARREN SK JABS EW
Citation: Af. Lewanda et al., EVIDENCE THAT THE SAETHRE-CHOTZEN SYNDROME LOCUS LIES BETWEEN D7S664 AND D7S507, BY GENETIC-ANALYSIS AND DETECTION OF A MICRODELETION IN A PATIENT, American journal of human genetics, 55(6), 1994, pp. 1195-1201
CYTOGENETIC SURVEY OF APERT SYNDROME - REEVALUATION OF A TRANSLOCATION (29)(P11.2Q34.2) IN A PATIENT SUGGESTS THE BREAKPOINTS ARE NOT RELATED TO THE DISORDER
Authors: LEWANDA AF COHEN MM HOOD J MORSEY S WALTERS M KENNEDY JL JABS EW
Citation: Af. Lewanda et al., CYTOGENETIC SURVEY OF APERT SYNDROME - REEVALUATION OF A TRANSLOCATION (29)(P11.2Q34.2) IN A PATIENT SUGGESTS THE BREAKPOINTS ARE NOT RELATED TO THE DISORDER, American journal of diseases of children [1960], 147(12), 1993, pp. 1306-1308
Risultati: 1-14 |