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Results:
1-15
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Results: 15
Authors:
GUIOLI S
SCHMITT K
CRITCHER R
BOUZYK M
SPURR NK
OGATA T
HOO JJ
PINSKY L
GIMELLI G
PASZTOR L
GOODFELLOW PN
Citation: S. Guioli et al., MOLECULAR ANALYSIS OF 9P DELETIONS ASSOCIATED WITH XY SEX REVERSAL - REFINING THE LOCALIZATION OF A SEX-DETERMINING GENE TO THE TIP OF THE CHROMOSOME, American journal of human genetics, 63(3), 1998, pp. 905-908
Authors:
ORTIGAS AP
STEIN CK
THOMSON LL
HOO JJ
Citation: Ap. Ortigas et al., DELINEATION OF 14Q32.3 DELETION SYNDROME, Journal of Medical Genetics, 34(6), 1997, pp. 515-517
Authors:
HOO JJ
Citation: Jj. Hoo, ACUPRESSURE FOR HYPEREMESIS GRAVIDARUM, American journal of obstetrics and gynecology, 176(6), 1997, pp. 1395-1396
Authors:
ISLAM MR
VERVOORT R
LISSENS W
HOO JJ
VALENTINO LA
SLY WS
Citation: Mr. Islam et al., BETA-GLUCURONIDASE P408S, P415L MUTATIONS - EVIDENCE THAT BOTH MUTATIONS COMBINE TO PRODUCE AN MPS-VII ALLELE IN CERTAIN MEXICAN PATIENTS, Human genetics, 98(3), 1996, pp. 281-284
Authors:
THOMSON LL
HOO JJ
Citation: Ll. Thomson et Jj. Hoo, LINEAR DISRUPTION OF UMBILICAL-CORD - A RARE ANOMALY OF THE CORD ASSOCIATED WITH ACUTE FETAL DISTRESS AND PERINATAL DEATH PROFOUND PSYCHOMOTOR RETARDATION, American journal of medical genetics, 62(4), 1996, pp. 348-349
Authors:
STEIN CK
STRED SE
THOMSON LL
SMITH FC
HOO JJ
Citation: Ck. Stein et al., INTERSTITIAL 6Q DELETION AND PRADER-WILLI-LIKE PHENOTYPE, Clinical genetics, 49(6), 1996, pp. 306-310
SUPERNUMERARY ISOCHROMOSOME 4P IN ANLL-M4 MYELOMONOCYTIC TYPE IS ASSOCIATED WITH FAVORABLE PROGNOSIS
Authors:
HOO JJ
GREGORY SA
JONES B
SZEGO K
Citation: Jj. Hoo et al., SUPERNUMERARY ISOCHROMOSOME 4P IN ANLL-M4 MYELOMONOCYTIC TYPE IS ASSOCIATED WITH FAVORABLE PROGNOSIS, Cancer genetics and cytogenetics, 79(2), 1995, pp. 127-129
Authors:
HOO JJ
CHAO M
SZEGO K
RAUER M
ECHIVERRI SC
HARRIS C
Citation: Jj. Hoo et al., 4 NEW CASES OF INVERTED TERMINAL DUPLICATION - A MODIFIED HYPOTHESIS OF MECHANISM OF ORIGIN, American journal of medical genetics, 58(4), 1995, pp. 299-304
Authors:
THOMSON LL
STEIN CK
KAWATU D
HOO JJ
Citation: Ll. Thomson et al., 2 CASES OF XP INTERSTITIAL TANDEM DUPLICATION - NO CORRELATION BETWEEN X-INACTIVATION PATTERN AND MENTAL STATUS IN 2 FEMALES OF ONE FAMILY,AND HYPOMELANOSIS OF ITO IN ANOTHER MOSAIC CASE, American journal of human genetics, 57(4), 1995, pp. 722-722
Authors:
HOO JJ
KREITER M
HALVERSON N
PERSZYK A
Citation: Jj. Hoo et al., 3C (CRANIO-CEREBELLO-CARDIAC) SYNDROME - A RECENTLY DELINEATED AND EASILY RECOGNIZABLE CONGENITAL-MALFORMATION SYNDROME, American journal of medical genetics, 52(1), 1994, pp. 66-69
Authors:
WEESEMAYER DE
SILVESTRI JM
MARAZITA ML
HOO JJ
Citation: De. Weesemayer et al., CONGENITAL CENTRAL HYPOVENTILATION SYNDROME - INHERITANCE AND RELATION TO SUDDEN-INFANT-DEATH-SYNDROME, American journal of medical genetics, 47(3), 1993, pp. 360-367
Authors:
HOO JJ
SZEGO K
WONG P
ROLAND B
Citation: Jj. Hoo et al., EVIDENCE OF CHROMOSOME-9 ORIGIN OF THE EUCHROMATIC VARIANT BAND WITHIN 9QH, Clinical genetics, 43(6), 1993, pp. 309-311
Authors:
SZEGO K
RAUER M
BARATTA E
HOO JJ
Citation: K. Szego et al., DE-NOVO CONCURRENT 5P DELETION AND DISTAL 17Q DUPLICATION IDENTIFIED BY FLUORESCENCE IN-SITU HYBRIDIZATION (FISH), Annales de genetique, 36(4), 1993, pp. 224-227
Authors:
HOO JJ
KREITER M
HALVERSON N
PERSZYK A
Citation: Jj. Hoo et al., 2 ADDITIONAL CASES OF 3-C (CRANIO-CEREBELLO-CARDIAC) SYNDROME - A RECENTLY DELINEATED AND EASILY RECOGNIZABLE CONGENITAL-MALFORMATION SYNDROME, American journal of human genetics, 53(3), 1993, pp. 449-449
Authors:
HOO JJ
Citation: Jj. Hoo, A NEW CHROMOSOME-9 VARIANT - AN EXTRA BAND WITHIN THE 9QH REGION, Clinical genetics, 41(3), 1992, pp. 157-158
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