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Results:
1-16
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Results: 16
Authors:
SCHULMAN JD
STERN HJ
Citation: Jd. Schulman et Hj. Stern, GENETIC PREDISPOSITION TESTING FOR BREAST-CANCER - REPLY, The cancer journal from Scientific American, 3(4), 1997, pp. 254-254
Authors:
HOPKIN RJ
SCHORRY E
BOFINGER M
MILATOVICH A
STERN HJ
JAYNE C
SAAL HM
Citation: Rj. Hopkin et al., NEW INSIGHTS INTO THE PHENOTYPES OF 6Q DELETIONS, American journal of medical genetics, 70(4), 1997, pp. 377-386
Authors:
RINALDO P
STANLEY CA
HSU BYL
SANCHEZ LA
STERN HJ
Citation: P. Rinaldo et al., SUDDEN NEONATAL DEATH IN CARNITINE TRANSPORTER DEFICIENCY, The Journal of pediatrics, 131(2), 1997, pp. 304-305
Authors:
BICK DP
STANLEY WS
STERN HJ
BERKOVITZ GD
MEYERS CM
KELLEY RI
Citation: Dp. Bick et al., PRENATAL-DIAGNOSIS OF SMITH-LEMLI-OPITZ-SYNDROME (SLO) IN A SEX-REVERSED FETUS, American journal of human genetics, 61(4), 1997, pp. 838-838
Authors:
STERN HJ
MADDALENA A
SCHULMAN JD
Citation: Hj. Stern et al., PITFALLS OF GENETIC TESTING, The New England journal of medicine, 335(16), 1996, pp. 1235-1235
Authors:
COHEN MS
SAMANGOSPROUSE C
STERN HJ
CUSTER DA
VAUGHT DR
SAAL HM
TIFFT CJ
ROSENBAUM KN
Citation: Ms. Cohen et al., NEURODEVELOPMENTAL PROFILE OF INFANTS AND TODDLERS WITH OCULO-AURICULO-VERTEBRAL SPECTRUM AND THE CORRELATION OF PROGNOSIS WITH PHYSICAL FINDINGS, American journal of medical genetics, 60(6), 1995, pp. 535-540
Authors:
STERN HJ
CARLOS RD
SCHUTZBANK TE
Citation: Hj. Stern et al., RAPID DETECTION OF THE DELTA-F508 DELETION IN CYSTIC-FIBROSIS BY ALLELE-SPECIFIC PCR AND ELECTROCHEMILUMINESCENT DETECTION, Clinical biochemistry, 28(4), 1995, pp. 470-473
Authors:
STERN HJ
NAYAR R
DEPALMA L
RIFAI N
Citation: Hj. Stern et al., PROLONGED SURVIVAL IN PYRUVATE-CARBOXYLASE DEFICIENCY - LACK OF CORRELATION WITH ENZYME-ACTIVITY IN CULTURED FIBROBLAST, Clinical biochemistry, 28(1), 1995, pp. 85-89
Authors:
SAAL HM
SCHORRY EK
LOVELL AM
BALL W
EGELHOFF J
KOCH B
SAMANGOSPROUSE A
ROSENBAUM KN
STERN HJ
TIFFT CJ
VEZINA LG
Citation: Hm. Saal et al., RACIAL-DIFFERENCES IN THE PREVALENCE OF OPTIC-NERVE GLIOMAS IN NEUROFIBROMATOSIS TYPE, American journal of human genetics, 57(4), 1995, pp. 280-280
Authors:
COHEN MS
SAMANGOSPROUSE CA
STERN HJ
ROSENBAUM KN
TIFFT CJ
Citation: Ms. Cohen et al., MACROCEPHALY IN NEUROFIBROMATOSIS TYPE-1, American journal of human genetics, 57(4), 1995, pp. 465-465
Authors:
HOPKIN RJ
SCHORRY EK
BOFINGER M
MILATOVICH T
STERN HJ
SAAL HM
Citation: Rj. Hopkin et al., NEW INSIGHTS INTO THE PHENOTYPES OF 6Q DELETIONS, American journal of human genetics, 57(4), 1995, pp. 647-647
Authors:
BULAS DI
STERN HJ
ROSENBAUM KN
FONDA JA
GLASS RBJ
TIFFT C
Citation: Di. Bulas et al., VARIABLE PRENATAL APPEARANCE OF OSTEOGENESIS IMPERFECTA, Journal of ultrasound in medicine, 13(6), 1994, pp. 419-427
Authors:
MOTT SH
SAMANGOSPROUSE CA
VENIZA LG
COHEN MS
TIFTT CJ
STERN HJ
SAUL HM
PACKER RJ
ROSENBAUM KN
Citation: Sh. Mott et al., NEUROFIBROMATOSIS TYPE-1 (NF-1) - CORRELATES BETWEEN NEURODEVELOPMENTAL PROFILE, HYPOTONIA AND FINDINGS IN MAGNETIC-RESONANCE-IMAGING (MR) IN YOUNG-CHILDREN, Neurology, 44(4), 1994, pp. 10000144-10000145
Authors:
STERN HJ
Citation: Hj. Stern, LACTIC-ACIDOSIS IN PEDIATRICS - CLINICAL AND LABORATORY EVALUATION, Annals of clinical biochemistry, 31, 1994, pp. 410-419
Authors:
STERN HJ
Citation: Hj. Stern, SCHIDROWITZ,PHILIP 1872-1960, Rubber chemistry and technology, 66(2), 1993, pp. 37-38
Authors:
MCLEAN SD
STERN HJ
ROSENBAUM KN
TIFFT CJ
SAAL HM
Citation: Sd. Mclean et al., THE NATURAL-HISTORY OF CAFE-AU-LAIT SPOTS IN YOUNG-CHILDREN WITH NEUROFIBROMATOSIS-1, American journal of human genetics, 53(3), 1993, pp. 474-474
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