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Results: 1-13 |
Results: 13
WEAVER-SYNDROME - AUTOSOMAL-DOMINANT INHERITANCE OF THE DISORDER
Authors: PROUD VK BRADDOCK SR COOK L WEAVER DD
Citation: Vk. Proud et al., WEAVER-SYNDROME - AUTOSOMAL-DOMINANT INHERITANCE OF THE DISORDER, American journal of medical genetics, 79(4), 1998, pp. 305-310
SYNDROME OF CORONAL CRANIOSYNOSTOSIS WITH BRACHYDACTYLY AND CARPAL TARSAL COALITION DUE TO PRO250ARG MUTATION IN FGFR3 GENE/
Authors: GRAHAM JM BRADDOCK SR MORTIER GR LACHMAN R VANDOP C JABS EW
Citation: Jm. Graham et al., SYNDROME OF CORONAL CRANIOSYNOSTOSIS WITH BRACHYDACTYLY AND CARPAL TARSAL COALITION DUE TO PRO250ARG MUTATION IN FGFR3 GENE/, American journal of medical genetics, 77(4), 1998, pp. 322-329
STEVENS-JOHNSON-SYNDROME AND RESPIRATORY-FAILURE IN A 9-YEAR-OLD BOY
Authors: SCHAMBERGER MS GOEL J BRADDOCK SR PARSONS DS TOBIAS JD
Citation: Ms. Schamberger et al., STEVENS-JOHNSON-SYNDROME AND RESPIRATORY-FAILURE IN A 9-YEAR-OLD BOY, Southern medical journal, 90(7), 1997, pp. 755-757
TRISOMY-21 - A CASE OF SEVERE GENOTYPE-PHENOTYPE DISCORDANCE
Authors: BRADDOCK SR WILLIAMSONKRUSE L PECKHAM D CHEN XN KORENBERG JR
Citation: Sr. Braddock et al., TRISOMY-21 - A CASE OF SEVERE GENOTYPE-PHENOTYPE DISCORDANCE, American journal of human genetics, 61(4), 1997, pp. 512-512
FURTHER DELINEATION OF RENAL-COLOBOMA SYNDROME IN PATIENTS WITH EXTREME VARIABILITY OF PHENOTYPE AND IDENTICAL PAX2 MUTATIONS
Authors: SCHIMMENTI LA CUNLIFFE HE MCNOE LA WARD TA FRENCH MC SHIM HH ZHANG YH PROESMANS W LEYS A BYERLY KA BRADDOCK SR MASUNO M IMAIZUMI K DEVRIENDT K ECCLES MR
Citation: La. Schimmenti et al., FURTHER DELINEATION OF RENAL-COLOBOMA SYNDROME IN PATIENTS WITH EXTREME VARIABILITY OF PHENOTYPE AND IDENTICAL PAX2 MUTATIONS, American journal of human genetics, 60(4), 1997, pp. 869-878
FRONTONASAL MALFORMATION AND THE OCULOAURICULOVERTEBRAL SPECTRUM - THE OCULOAURICULOFRONTONASAL SYNDROME
Authors: CASEY HD BRADDOCK SR HASKINS RC CAREY JC MORALES L
Citation: Hd. Casey et al., FRONTONASAL MALFORMATION AND THE OCULOAURICULOVERTEBRAL SPECTRUM - THE OCULOAURICULOFRONTONASAL SYNDROME, The Cleft palate-craniofacial journal, 33(6), 1996, pp. 519-523
ANTERIOR CERVICAL HYPERTRICHOSIS - A DOMINANTLY INHERITED ISOLATED DEFECT
Authors: BRADDOCK SR JONES KL BIRD LM VILLEGAS I JONES MC
Citation: Sr. Braddock et al., ANTERIOR CERVICAL HYPERTRICHOSIS - A DOMINANTLY INHERITED ISOLATED DEFECT, American journal of medical genetics, 55(4), 1995, pp. 498-499
DEVELOPMENT OF THE OLFACTORY NERVE - ITS RELATIONSHIP TO THE CRANIOFACIES
Authors: BRADDOCK SR GRAFE MR JONES KL
Citation: Sr. Braddock et al., DEVELOPMENT OF THE OLFACTORY NERVE - ITS RELATIONSHIP TO THE CRANIOFACIES, Teratology, 51(4), 1995, pp. 252-256
BILATERAL FIBULAR HYPOPLASIA - A DOMINANT DISORDER WITH VARIABLE EXPRESSIVITY
Authors: BRADDOCK SR JONES KL SALAFSKY IS MILLAR EA
Citation: Sr. Braddock et al., BILATERAL FIBULAR HYPOPLASIA - A DOMINANT DISORDER WITH VARIABLE EXPRESSIVITY, Clinical research, 42(1), 1994, pp. 10000050-10000050
HAIRY THROAT - A DOMINANTLY INHERITED ISOLATED DEFECT
Authors: BRADDOCK SR JONES KL BIRD LM VILLEGAS I JONES MC
Citation: Sr. Braddock et al., HAIRY THROAT - A DOMINANTLY INHERITED ISOLATED DEFECT, Clinical research, 42(1), 1994, pp. 10000065-10000065
RADIOLOGICAL FEATURES IN BRACHMANN-DELANGE SYNDROME
Authors: BRADDOCK SR LACHMAN RS STOPPENHAGEN CC CAREY JC IRELAND M MOESCHLER JB CUNNIFF C GRAHAM JM
Citation: Sr. Braddock et al., RADIOLOGICAL FEATURES IN BRACHMANN-DELANGE SYNDROME, American journal of medical genetics, 47(7), 1993, pp. 1006-1013
SAGITTAL CRANIOSYNOSTOSIS, DANDY-WALKER MALFORMATION, AND HYDROCEPHALUS - A UNIQUE MULTIPLE MALFORMATION SYNDROME
Authors: BRADDOCK SR JONES KL SUPERNEAU DW JONES MC
Citation: Sr. Braddock et al., SAGITTAL CRANIOSYNOSTOSIS, DANDY-WALKER MALFORMATION, AND HYDROCEPHALUS - A UNIQUE MULTIPLE MALFORMATION SYNDROME, American journal of medical genetics, 47(5), 1993, pp. 640-643
RETT-SYNDROME - AN UPDATE AND REVIEW FOR THE PRIMARY PEDIATRICIAN
Authors: BRADDOCK SR BRADDOCK BA GRAHAM JM
Citation: Sr. Braddock et al., RETT-SYNDROME - AN UPDATE AND REVIEW FOR THE PRIMARY PEDIATRICIAN, Clinical pediatrics, 32(10), 1993, pp. 613-626
Risultati: 1-13 |