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Results: 1-25 | 26-50 |
Results: 26-50/50
MOLECULAR CYTOGENETIC CHARACTERIZATION OF BREAKPOINTS INVOLVING PERICENTRIC INVERSIONS OF HUMAN-CHROMOSOME-9
Authors: SAMONTE RV CONTE RA RAMESH KH VERMA RS
Citation: Rv. Samonte et al., MOLECULAR CYTOGENETIC CHARACTERIZATION OF BREAKPOINTS INVOLVING PERICENTRIC INVERSIONS OF HUMAN-CHROMOSOME-9, Human genetics, 98(5), 1996, pp. 576-580
TO RULE OUT CHROMOSOMAL-ABNORMALITIES - A SAGACIOUS VIEW
Authors: VERMA RS KLEYMAN SM AZAR GM CONTE RA
Citation: Rs. Verma et al., TO RULE OUT CHROMOSOMAL-ABNORMALITIES - A SAGACIOUS VIEW, Lancet, 348(9035), 1996, pp. 1173-1174
A UNIQUE GENOMIC SEQUENCE IN THE WOLF-HIRSCHHORN SYNDROME [WHS] REGION OF HUMANS IS CONSERVED IN THE GREAT APES
Authors: TARZAMI ST KRINGSTEIN AM CONTE RA VERMA RS
Citation: St. Tarzami et al., A UNIQUE GENOMIC SEQUENCE IN THE WOLF-HIRSCHHORN SYNDROME [WHS] REGION OF HUMANS IS CONSERVED IN THE GREAT APES, Genetica, 98(2), 1996, pp. 217-219
MOLECULAR CHARACTERIZATION OF 21P-VARIANT CHROMOSOME
Authors: CONTE RA MATHEWS T KLEYMAN SM VERMA RS
Citation: Ra. Conte et al., MOLECULAR CHARACTERIZATION OF 21P-VARIANT CHROMOSOME, Clinical genetics, 50(2), 1996, pp. 103-105
CENTROMERIC ALPHOID SEQUENCES ARE BREAKAGE PRONE RESULTING IN PERICENTROMERIC INVERSION HETEROMORPHISM OF QH REGION OF CHROMOSOME-1
Authors: VERMA RS RAMESH KH MATHEWS T KLEYMAN SM CONTE RA
Citation: Rs. Verma et al., CENTROMERIC ALPHOID SEQUENCES ARE BREAKAGE PRONE RESULTING IN PERICENTROMERIC INVERSION HETEROMORPHISM OF QH REGION OF CHROMOSOME-1, Annales de genetique, 39(4), 1996, pp. 205-208
CHARACTERIZATION OF A DE-NOVO T(Y-9)(Q11.2-Q22) BY FISH TECHNIQUE
Authors: CONTE RA KLEYMAN SM KLEIN V BIALER MG VERMA RS
Citation: Ra. Conte et al., CHARACTERIZATION OF A DE-NOVO T(Y-9)(Q11.2-Q22) BY FISH TECHNIQUE, Annales de genetique, 39(1), 1996, pp. 10-15
ENUMERATION OF SEMEN LEUKOCYTES BY FLUORESCENCE IN-SITU HYBRIDIZATIONTECHNIQUE
Authors: CONTE RA LUKE S VERMA RS
Citation: Ra. Conte et al., ENUMERATION OF SEMEN LEUKOCYTES BY FLUORESCENCE IN-SITU HYBRIDIZATIONTECHNIQUE, JCP. Clinical molecular pathology, 48(6), 1995, pp. 319-321
CLINICAL MANIFESTATIONS OF TRISOMY 4P SYNDROME
Authors: PATEL SV DAGNEW H PAREKH AJ KOENIG E CONTE RA MACERA MJ VERMA RS
Citation: Sv. Patel et al., CLINICAL MANIFESTATIONS OF TRISOMY 4P SYNDROME, European journal of pediatrics, 154(6), 1995, pp. 425-431
MECHANISMS OF THE ORIGIN OF A G-POSITIVE BAND WITHIN THE SECONDARY CONSTRICTION REGION OF HUMAN-CHROMOSOME-9
Authors: MACERA MJ VERMA RS CONTE RA BIALER MG KLEIN VR
Citation: Mj. Macera et al., MECHANISMS OF THE ORIGIN OF A G-POSITIVE BAND WITHIN THE SECONDARY CONSTRICTION REGION OF HUMAN-CHROMOSOME-9, Cytogenetics and cell genetics, 69(3-4), 1995, pp. 235-239
RARE VARIANTS OF CHROMOSOME-9 WITH EXTRA G-POSITIVE BAND WITHIN THE QH REGION ARE NOT ALIKE
Authors: CONTE RA GUPTA S BRENNAN JP VERMA RS
Citation: Ra. Conte et al., RARE VARIANTS OF CHROMOSOME-9 WITH EXTRA G-POSITIVE BAND WITHIN THE QH REGION ARE NOT ALIKE, Journal of Medical Genetics, 32(5), 1995, pp. 405-406
CHARACTERIZATION OF A RING CHROMOSOME-21 BY FISH-TECHNIQUE
Authors: CONTE RA LUKE S VERMA RS
Citation: Ra. Conte et al., CHARACTERIZATION OF A RING CHROMOSOME-21 BY FISH-TECHNIQUE, Clinical genetics, 48(4), 1995, pp. 188-191
MOLECULAR CHARACTERIZATION OF TRISOMIC SEGMENT 3P24.1-]PTER - A CASE WITH REVIEW OF THE LITERATURE
Authors: CONTE RA PITTER JH VERMA RS
Citation: Ra. Conte et al., MOLECULAR CHARACTERIZATION OF TRISOMIC SEGMENT 3P24.1-]PTER - A CASE WITH REVIEW OF THE LITERATURE, Clinical genetics, 48(1), 1995, pp. 49-53
CORRELATION BETWEEN SPERMATOZOA AND CHROMOSOMAL SELECTION USING A SUPRAVITAL STAIN AND FISH
Authors: CONTE RA VERMA RS
Citation: Ra. Conte et Rs. Verma, CORRELATION BETWEEN SPERMATOZOA AND CHROMOSOMAL SELECTION USING A SUPRAVITAL STAIN AND FISH, American journal of human genetics, 57(4), 1995, pp. 748-748
MOLECULAR CHARACTERIZATION OF A DE-NOVO T(Y-9)(Q11.2-Q22) BY FISH TECHNIQUE
Authors: KLEIN V CONTE RA BIALER MG KLEYMAN S VERMA RS
Citation: V. Klein et al., MOLECULAR CHARACTERIZATION OF A DE-NOVO T(Y-9)(Q11.2-Q22) BY FISH TECHNIQUE, American journal of human genetics, 57(4), 1995, pp. 1799-1799
TANDEM DUPLICATION OF BETA-SATELLITE, SATELLITE-III AND RDNA RESULTING IN AN EXTREME VARIANT OF CHROMOSOME 22P
Authors: KLEYMAN S CONTE RA VERMA RS
Citation: S. Kleyman et al., TANDEM DUPLICATION OF BETA-SATELLITE, SATELLITE-III AND RDNA RESULTING IN AN EXTREME VARIANT OF CHROMOSOME 22P, American journal of human genetics, 57(4), 1995, pp. 1800-1800
COMPLETE DELETION OF SHORT ARM OF CHROMOSOME-21
Authors: MATHEWS T CONTE RA KLEYMAN S VERMA RS
Citation: T. Mathews et al., COMPLETE DELETION OF SHORT ARM OF CHROMOSOME-21, American journal of human genetics, 57(4), 1995, pp. 1804-1804
AN UNUSUAL EUCHROMATIC BAND WITHIN THE SECONDARY CONSTRICTION (QH) REGION OF HUMAN-CHROMOSOME-1
Authors: VERMA RS KLEYMAN S CONTE RA
Citation: Rs. Verma et al., AN UNUSUAL EUCHROMATIC BAND WITHIN THE SECONDARY CONSTRICTION (QH) REGION OF HUMAN-CHROMOSOME-1, American journal of human genetics, 57(4), 1995, pp. 1809-1809
FISH TECHNIQUE - WHATS ALL THE FUSS ABOUT
Authors: VERMA RS LUKE S CONTE RA
Citation: Rs. Verma et al., FISH TECHNIQUE - WHATS ALL THE FUSS ABOUT, GENET A-BIO, 11(4), 1994, pp. 106-109
AN APPARENT BALANCED TRANSLOCATION BETWEEN CHROMOSOME-7 AND CHROMOSOME-13 [T(7-13) (P15-Q32)] IN A 47,XYY INDIVIDUAL
Authors: VERMA RS GIRIDHARAN R CONTE RA LUKE S
Citation: Rs. Verma et al., AN APPARENT BALANCED TRANSLOCATION BETWEEN CHROMOSOME-7 AND CHROMOSOME-13 [T(7-13) (P15-Q32)] IN A 47,XYY INDIVIDUAL, JPN J HUM G, 39(4), 1994, pp. 451-452
MONOZYGOTIC TWINNING IN A FEMALE WITH TRIPLE X[47,XXX]
Authors: VERMA RS CONTE RA MATHEWS T LUKE S
Citation: Rs. Verma et al., MONOZYGOTIC TWINNING IN A FEMALE WITH TRIPLE X[47,XXX], Gynecologic and obstetric investigation, 37(4), 1994, pp. 279-280
COUNTERSTAINED ENHANCEMENT OF TAQI RESISTANT SITES AFTER DISTAMYCIN ADIAMIDINOPHENYLINDOLE TREATMENT
Authors: CONTE RA VERMA RS
Citation: Ra. Conte et Rs. Verma, COUNTERSTAINED ENHANCEMENT OF TAQI RESISTANT SITES AFTER DISTAMYCIN ADIAMIDINOPHENYLINDOLE TREATMENT, Histochemistry, 102(6), 1994, pp. 433-435
2 PRADER-WILLI-ANGELMAN-SYNDROME LOCI PRESENT IN AN ISODICENTRIC MARKER CHROMOSOME
Authors: LUKE S VERMA RS GIRIDHARAN R CONTE RA MACERA MJ
Citation: S. Luke et al., 2 PRADER-WILLI-ANGELMAN-SYNDROME LOCI PRESENT IN AN ISODICENTRIC MARKER CHROMOSOME, American journal of medical genetics, 51(3), 1994, pp. 232-233
MOLECULAR CHARACTERIZATION OF A RING CHROMOSOME-21 IN DOWN-SYNDROME
Authors: CONTE RA LUKE S VERMA RS
Citation: Ra. Conte et al., MOLECULAR CHARACTERIZATION OF A RING CHROMOSOME-21 IN DOWN-SYNDROME, American journal of human genetics, 53(3), 1993, pp. 536-536
MOLECULAR CHARACTERIZATION OF A MARKER CHROMOSOME IN AN INDIVIDUAL WITH HYPOTONIC AND GLOBAL DEVELOPMENTAL DELAY
Authors: GIRIDHARAN R CONTE RA LUKE S MACERA MJ VERMA RS
Citation: R. Giridharan et al., MOLECULAR CHARACTERIZATION OF A MARKER CHROMOSOME IN AN INDIVIDUAL WITH HYPOTONIC AND GLOBAL DEVELOPMENTAL DELAY, American journal of human genetics, 53(3), 1993, pp. 551-551
MOLECULAR TOPOGRAPHY OF THE SECONDARY CONSTRICTION REGION (QH) OF HUMAN CHROMOSOME-9 WITH AN UNUSUAL EUCHROMATIC BAND
Authors: VERMA RS LUKE S BRENNAN JP MATHEWS T CONTE RA MACERA MJ
Citation: Rs. Verma et al., MOLECULAR TOPOGRAPHY OF THE SECONDARY CONSTRICTION REGION (QH) OF HUMAN CHROMOSOME-9 WITH AN UNUSUAL EUCHROMATIC BAND, American journal of human genetics, 52(5), 1993, pp. 981-986
Risultati: 1-25 | 26-50 |