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ALANO A
ALMASHANU S
CHINSKY JM
COSTEAS P
BLITZER MG
WULFSBERG EA
COWAN TM
Citation: A. Alano et al., MOLECULAR CHARACTERIZATION OF A UNIQUE PATIENT WITH EPIMERASE-DEFICIENCY GALACTOSEMIA, Journal of inherited metabolic disease, 21(4), 1998, pp. 341-350
Authors:
BEATY TH
MAESTRI NE
HETMANSKI JB
WYSZYNSKI DF
VANDERKOLK CA
SIMPSON JC
MCINTOSH I
SMITH EA
ZEIGER JS
RAYMOND GV
PANNY SR
TIFFT CJ
LEWANDA AF
CRISTION CA
WULFSBERG EA
Citation: Th. Beaty et al., TESTING FOR INTERACTION BETWEEN MATERNAL SMOKING AND TGFA GENOTYPE AMONG ORAL CLEFT CASES BORN IN MARYLAND 1992-1996, The Cleft palate-craniofacial journal, 34(5), 1997, pp. 447-454
Authors:
LEE DH
SANDERS RC
MEYERS CM
WULFSBERG EA
SUN CCJ
Citation: Dh. Lee et al., THE OEIS COMPLEX (OMPHALOCELE-EXSTROPHY-IMPERFORATE ANUS-SPINAL DEFECTS) IN MONOZYGOTIC TWINS, Laboratory investigation, 76(1), 1997, pp. 12-12
Authors:
TRETTER AE
SAUNDERS RC
MEYERS CM
DUNGAN JS
GRUMBACH K
SUN CJ
CAMPBELL AB
WULFSBERG EA
Citation: Ae. Tretter et al., ANTENATAL DIAGNOSIS AND OUTCOME OF LETHAL SKELETAL DYSPLASIAS, American journal of human genetics, 61(4), 1997, pp. 650-650
Authors:
LEANACOX J
PANGKANON S
EANET KR
CURTIN MS
WULFSBERG EA
Citation: J. Leanacox et al., FAMILIAL DIGEORGE VELOCARDIOFACIAL SYNDROME WITH DELETIONS OF CHROMOSOME AREA 22Q11.2 - REPORT OF 5 FAMILIES WITH A REVIEW OF THE LITERATURE/, American journal of medical genetics, 65(4), 1996, pp. 309-316
Citation: Ea. Wulfsberg et al., WHATS IN A NAME - CHROMOSOME 22Q ABNORMALITIES AND THE DIGEORGE, VELOCARDIOFACIAL, AND CONOTRUNCAL ANOMALIES FACE SYNDROMES, American journal of medical genetics, 65(4), 1996, pp. 317-319
Citation: Ea. Wulfsberg, IS THE AUTOSOMAL-DOMINANT OPITZ GBBB SYNDROME PART OF THE DIGEORGE VELOCARDIOFACIAL SYNDROME WITH DELETIONS OF CHROMOSOME AREA 22Q11.2/, American journal of medical genetics, 64(3), 1996, pp. 523-524
Authors:
WULFSBERG EA
CAMPBELL AB
LURIE IW
EANET KR
Citation: Ea. Wulfsberg et al., CONFIRMATION OF THE CATANIA BRACHYDACTYLOUS TYPE OF ACROFACIAL DYSOSTOSIS - REPORT OF A 2ND FAMILY, American journal of medical genetics, 63(4), 1996, pp. 554-557
Citation: De. Hoffmann et Ea. Wulfsberg, TESTING CHILDREN FOR GENETIC PREDISPOSITIONS - IS IT IN THEIR BEST INTEREST, The Journal of law, medicine & ethics, 23(4), 1995, pp. 331-344
Authors:
LEANACOX J
PANGKANON S
SUPOVITZ KR
CURTIN MS
WULFSBERG EA
Citation: J. Leanacox et al., PHENOTYPIC VARIABILITY ASSOCIATED WITH DEL(22)(Q11.2) - A REPORT OF 5FAMILIAL CASES, American journal of human genetics, 57(4), 1995, pp. 523-523
Citation: Kr. Supovitz et Ea. Wulfsberg, 3 YEAR FOLLOW-UP OF A PATIENT WITH TORIELLO-CAREY-SYNDROME, American journal of human genetics, 57(4), 1995, pp. 574-574
Authors:
HOGGE WA
BLANK C
ROOCHVARG LB
HOGGE JS
WULFSBERG EA
RAFFEL LJ
Citation: Wa. Hogge et al., GORLIN SYNDROME (NEVOID BASAL-CELL CARCINOMA SYNDROME) - PRENATAL DETECTION IN A FETUS WITH MACROCEPHALY AND VENTRICULOMEGALY, Prenatal diagnosis, 14(8), 1994, pp. 725-727
Citation: Ea. Wulfsberg et al., ALPHA-1-ANTITRYPSIN DEFICIENCY - IMPACT OF GENETIC DISCOVERY ON MEDICINE AND SOCIETY, JAMA, the journal of the American Medical Association, 271(3), 1994, pp. 217-222
Authors:
LURIE IW
WULFSBERG EA
PRABHAKAR G
ROSENBLUMVOS LS
SUPOVITZ KR
COHEN MM
Citation: Iw. Lurie et al., COMPLEX CHROMOSOMAL REARRANGEMENTS - SOME BREAKPOINTS MAY HAVE CELLULAR ADAPTIVE SIGNIFICANCE, Clinical genetics, 46(3), 1994, pp. 244-247
Citation: Iw. Lurie et Ea. Wulfsberg, ON THE NOSOLOGY OF THE SCHINZEL-PHOCOMELIA AND AL-AWADI RAAS-ROTHSCHIELD SYNDROMES/, American journal of medical genetics, 47(8), 1993, pp. 1234-1234
Citation: Iw. Lurie et Ea. Wulfsberg, HOLOPROSENCEPHALY-POLYDACTYLY (PSEUDOTRISOMY-13) SYNDROME - EXPANSIONOF THE PHENOTYPIC SPECTRUM, American journal of medical genetics, 47(3), 1993, pp. 405-409
Citation: Kr. Supovitz et Ea. Wulfsberg, FAMILY SUPPORT GROUP INVOLVEMENT IN A RESEARCH STUDY, American journal of human genetics, 53(3), 1993, pp. 1638-1638