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Results:
1-8
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Results: 8
Authors:
SALBERT BA
RADTKE HB
Citation: Ba. Salbert et Hb. Radtke, A REVIEW OF THE ROLE OF GENETICS IN CLEFT-LIP AND PALATE CLINIC, Journal of investigative medicine, 44(1), 1996, pp. 8-8
Authors:
SALBERT BA
SCHWARTZ ID
GRUNT JA
Citation: Ba. Salbert et al., SEX REVERSAL IN AN INFANT WITH SMITH-LEMLI-OPITZ SYNDROME, TYPE-II - EVIDENCE FOR 5-ALPHA REDUCTASE DEFICIENCY, Journal of pediatric endocrinology & metabolism, 9(1), 1996, pp. 67-69
Authors:
REYNOLDS JE
ARNOS KS
LANDA B
STEVENS CA
SALBERT BA
WRIGHT L
DUKE B
HUNT W
MARAZITA ML
PLOUGHMAN L
MACLEAN C
NANCE WE
DIEHL SR
Citation: Je. Reynolds et al., ANALYSIS OF LOCUS HETEROGENEITY IN WAARDENBURG-SYNDROME TYPE-1 AND TYPE-2 USING HIGHLY INFORMATIVE MICROSATELLITE MARKERS, Human heredity, 45(5), 1995, pp. 243-252
Authors:
COLE H
HUANG B
SALBERT BA
BROWN J
HOWARDPEEBLES PN
BLACK SH
DORFMANN A
FEBLES OR
STEVENS CA
JACKSONCOOK C
Citation: H. Cole et al., MENTAL-RETARDATION AND ULLRICH-TURNER SYNDROME IN CASES WITH 45,X 46,X,+MAR - ADDITIONAL SUPPORT FOR THE LOSS OF THE X-INACTIVATION CENTER HYPOTHESIS/, American journal of medical genetics, 52(2), 1994, pp. 136-145
Authors:
SALBERT BA
ASTRUC J
WOLF B
Citation: Ba. Salbert et al., OPHTHALMOLOGIC FINDINGS IN BIOTINIDASE DEFICIENCY, Ophthalmologica, 206(4), 1993, pp. 177-181
Authors:
SALBERT BA
PELLOCK JM
WOLF B
Citation: Ba. Salbert et al., CHARACTERIZATION OF SEIZURES ASSOCIATED WITH BIOTINIDASE DEFICIENCY, Neurology, 43(7), 1993, pp. 1351-1355
Authors:
EDDY MC
WINCHESTER P
FREEMAN JC
SALBERT BA
Citation: Mc. Eddy et al., LACRIMO-AURICULO-DENTO-DIGITAL SYNDROME WITH CHOANAL ATRESIA - EXPANDING THE PHENOTYPE, Clinical research, 41(4), 1993, pp. 10000790-10000790
Authors:
SALBERT BA
SOLOMON M
SPENCE JE
JACKSONCOOK C
BROWN J
BODURTHA J
Citation: Ba. Salbert et al., PARTIAL TRISOMY-19P - CASE-REPORT AND NATURAL-HISTORY, Clinical genetics, 41(3), 1992, pp. 143-146
Risultati:
1-8
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