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Results:
1-16
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Results: 16
Authors:
SHANSKE AL
GRUNWALD H
COOK P
HEISTERKAMP N
GROFFEN J
Citation: Al. Shanske et al., PHILADELPHIA-NEGATIVE CHRONIC MYELOGENOUS LEUKEMIA IN A PATIENT WITH A UNIQUE COMPLEX TRANSLOCATION - 46,XY,T(9-12-15)(Q34-Q12-Q21), Leukemia research, 22(7), 1998, pp. 645-648
Authors:
PATICOFF K
MARION RW
SHPRINTZEN RJ
SHANSKE AL
EISIG SB
Citation: K. Paticoff et al., HEMIMAXILLOFACIAL DYSPLASIA - A REPORT OF 2 NEW CASES AND FURTHER DELINEATION OF THE DISORDER, Oral surgery, oral medicine, oral pathology, oral radiology and endodontics, 83(4), 1997, pp. 484-488
Authors:
SHANSKE AL
BOGDANOW A
SHPRINTZEN RJ
MARION RW
Citation: Al. Shanske et al., THE MARSHALL-SYNDROME - REPORT OF A NEW FAMILY AND REVIEW OF THE LITERATURE, American journal of medical genetics, 70(1), 1997, pp. 52-57
Authors:
ELSCHAHAWI M
DEMUNAIN AL
SARRAZIN AM
SHANSKE AL
BASIRICO M
SHANSKE S
DIMAURO S
Citation: M. Elschahawi et al., 2 LARGE SPANISH PEDIGREES WITH NONSYNDROMIC SENSORINEURAL DEAFNESS AND THE MTDNA MUTATION AT NT-1555 IN THE 12S RIBOSOMAL-RNA GENE - EVIDENCE OF HETEROPLASMY, Neurology, 48(2), 1997, pp. 453-456
Authors:
HOFFMAN JD
SHANSKE AL
Citation: Jd. Hoffman et Al. Shanske, TRENDS IN FETAL-ALCOHOL-SYNDROME - ALBERT-EINSTEIN-COLLEGE-OF-MEDICINE AFFILIATED HOSPITALS, 1985-1996, American journal of human genetics, 61(4), 1997, pp. 2256-2256
Authors:
BERNSTEIN PS
GROSS SJ
COHEN DJ
TILLER GR
SHANSKE AL
BOMBARD AT
MARION RW
Citation: Ps. Bernstein et al., PRENATAL-DIAGNOSIS OF TYPE-2 PFEIFFER SYNDROME, Ultrasound in obstetrics & gynecology, 8(6), 1996, pp. 425-428
Authors:
CHIU NC
QIAN WH
SHANSKE AL
BROOKS SS
BOUSTANY RM
Citation: Nc. Chiu et al., A COMMON MUTATION SITE IN THE BETA-GALACTOSIDASE GENE ORIGINATES IN PUERTO-RICO, Pediatric neurology, 14(1), 1996, pp. 53-56
Authors:
SHANSKE AL
PRAKASHCHENG A
SHPRINTZEN RJ
Citation: Al. Shanske et al., THE OCCURRENCE OF VELOPHARYNGEAL INSUFFICIENCY IN PRIMARY MYOPATHIES, Pediatric research, 39(4), 1996, pp. 2268-2268
Authors:
SHANSKE AL
KALMAN A
GRUNWALD H
Citation: Al. Shanske et al., A MYELOPROLIFERATIVE DISORDER WITH EOSINOPHILIA ASSOCIATED WITH A UNIQUE TRANSLOCATION (3-5), British Journal of Haematology, 95(3), 1996, pp. 524-526
Authors:
SHANSKE AL
SEIMON LP
DORFMAN HD
HABERMAN ET
Citation: Al. Shanske et al., HEMIHYPERTROPHY IN A 10-YEAR OLD WITH OSTEOSARCOMA, Pediatric research, 37(4), 1995, pp. 165-165
Authors:
EISIG S
MARION R
SHPRINTZEN R
SHANSKE AL
Citation: S. Eisig et al., HEMIMAXILLOFACIAL DYSPLASIA - A REPORT OF 2 NEW CASES AND FURTHER DELINEATION OF THE DISORDER, American journal of human genetics, 57(4), 1995, pp. 478-478
Authors:
KIM ES
BOGDANOW A
MENASSEPALMER L
MARION R
SHANSKE AL
Citation: Es. Kim et al., CYSTIC HYGROMA AND MASSIVE HYDROPS IN A 45,X FETUS WITH OBSTRUCTIVE UROPATHY, American journal of human genetics, 57(4), 1995, pp. 1798-1798
Authors:
LEVY PA
SHANSKE AL
SCHMIDT R
Citation: Pa. Levy et al., DOUBLE ANEUPLOIDY - TRISOMY-21 AND CRI DU CHAT, American journal of human genetics, 57(4), 1995, pp. 1801-1801
Authors:
SHANSKE AL
LEE B
Citation: Al. Shanske et B. Lee, ABSENCE OF COL2A1 DEFECT IN THE MARSHALL SYNDROME (MIM NO.154780), American journal of human genetics, 57(4), 1995, pp. 1977-1977
Authors:
SHANSKE AL
SUN M
PARNES B
GATTI RA
Citation: Al. Shanske et al., SPONTANEOUS CHROMOSOME BREAKAGE IN ATAXIA-TELANGIECTASIA (A-T) HETEROZYGOTES, Pediatric research, 35(4), 1994, pp. 10000154-10000154
Authors:
SHANSKE AL
KROGH J
Citation: Al. Shanske et J. Krogh, BILATERAL TIBIAL APLASIA WITH FAMILIAL TRANSLOCATION AT CHROMOSOME-1Q41 AND CHROMOSOME-14Q13, Pediatric research, 35(4), 1994, pp. 10000154-10000154
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