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Results:
1-17
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Results: 17
Authors:
JACOBSON Z
GLICKSTEIN J
HENSLE T
MARION RW
Citation: Z. Jacobson et al., FURTHER DELINEATION OF THE OPITZ-G BBB-SYNDROME - REPORT OF AN INFANTWITH COMPLEX CONGENITAL HEART-DISEASE AND BLADDER EXSTROPHY, AND REVIEW OF THE LITERATURE/, American journal of medical genetics, 78(3), 1998, pp. 294-299
Authors:
ROBIN NH
SCOTT JA
ARNOLD JE
GOLDSTEIN JA
SHILLING BB
MARION RW
COHEN MM
Citation: Nh. Robin et al., FAVORABLE PROGNOSIS FOR CHILDREN WITH PFEIFFER-SYNDROME TYPE-2 AND TYPE-3 - IMPLICATIONS FOR CLASSIFICATION, American journal of medical genetics, 75(3), 1998, pp. 240-244
Authors:
SHANSKE A
BOGDANOW A
SHPRINTZEN RJ
MARION RW
Citation: A. Shanske et al., MARSHALL-SYNDROME AND A DEFECT AT THE COL11A1 LOCUS, American journal of human genetics, 63(5), 1998, pp. 1558-1559
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:
QUADERI NA
SCHWEIGER S
GAUDENZ K
FRANCO B
RUGARLI EI
BERGER W
FELDMAN GJ
VOLTA M
ANDOLFI G
GILGENKRANTZ S
MARION RW
HENNEKAM RCM
OPITZ JM
MUENKE M
ROPERS HH
BALLABIO A
Citation: Na. Quaderi et al., OPITZ G BBB SYNDROME, A DEFECT OF MIDLINE DEVELOPMENT, IS DUE TO MUTATIONS IN A NEW RING FINGER GENE ON XP22/, Nature genetics, 17(3), 1997, pp. 285-291
Authors:
SHANSKE A
CARIDE DG
MENASSEPALMER L
BOGDANOW A
MARION RW
Citation: A. Shanske et al., CENTRAL-NERVOUS-SYSTEM ANOMALIES IN SECKEL-SYNDROME - REPORT OF A NEWFAMILY AND REVIEW OF THE LITERATURE, American journal of medical genetics, 70(2), 1997, pp. 155-158
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:
MARION RW
Citation: Rw. Marion, PROBLEM OF OFFERING UNSOLICITED CLINICAL GENETIC ADVICE AND DIAGNOSESTO NONMEDICAL FRIENDS AND STRANGERS - RESPONSE TO DR HOOK, American journal of medical genetics, 68(4), 1997, pp. 486-486
Authors:
JACOBSON Z
GLICKSTEIN J
HENSEL T
MARION RW
Citation: Z. Jacobson et al., FURTHER DELINEATION OF THE OPITZ G BBB SYNDROME (OS) - REPORT OF A CHILD WITH COMPLEX CONGENITAL HEART-DISEASE (CCHD) AND BLADDER EXSTROPHY/, American journal of human genetics, 61(4), 1997, pp. 570-570
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:
MARION RW
Citation: Rw. Marion, THE CHRISTMAS PRESENT, American journal of medical genetics, 66(3), 1996, pp. 247-249
Authors:
MARION RW
Citation: Rw. Marion, GENETIC DRIFT - THE UNSOLVABLE PUZZLE, American journal of medical genetics, 62(4), 1996, pp. 327-329
Authors:
MARION RW
Citation: Rw. Marion, GENETIC DRIFT - THE SKELETON IN MR-ANDERSON-CLOSET, American journal of medical genetics, 59(1), 1995, pp. 1-3
Authors:
GLICKSTEIN J
KARASIK J
CARIDE DG
MARION RW
Citation: J. Glickstein et al., C TRIGONOCEPHALY SYNDROME - REPORT OF A CHILD WITH AGENESIS OF THE CORPUS-CALLOSUM AND TETRALOGY OF FALLOT, AND REVIEW, American journal of medical genetics, 56(2), 1995, pp. 215-218
Authors:
MARION RW
GARCIA DM
KARASIK JB
Citation: Rw. Marion et al., APPARENT DOMINANT TRANSMISSION OF THE RUBINSTEIN-TAYBI SYNDROME, American journal of medical genetics, 46(3), 1993, pp. 284-287
Authors:
SALOMON M
RAMASWAMY P
GARCIA D
MARION RW
Citation: M. Salomon et al., HYPERTHERMIA AS A COMPLICATION OF PRADER-WILLI-SYNDROME (PWS) - REPORT OF 2 ADDITIONAL PATIENTS, American journal of human genetics, 53(3), 1993, pp. 500-500
Authors:
MARION RW
Citation: Rw. Marion, DID NAPOLEON HAVE THE LATE-ONSET FORM OF 17-KETOSTEROID REDUCTASE DEFICIENCY, American journal of human genetics, 53(3), 1993, pp. 1674-1674
Risultati:
1-17
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