Authors:
MATSUOKA R
KIMURA M
SCAMBLER PJ
MORROW BE
IMAMURA S
MINOSHIMA S
SHIMIZU N
YAMAGISHI H
JOHO K
WATANABE S
OYAMA K
SAJI T
ANDO M
TAKAO A
MOMMA K
Citation: R. Matsuoka et al., MOLECULAR AND CLINICAL-STUDY OF 183 PATIENTS WITH CONOTRUNCAL ANOMALYFACE SYNDROME, Human genetics, 103(1), 1998, pp. 70-80
Authors:
FUNKE B
SAINTJORE B
PUECH A
SIROTKIN H
EDELMANN L
CARLSON C
RAFT S
PANDITA RK
KUCHERLAPATI R
SKOULTCHI A
MORROW BE
Citation: B. Funke et al., CHARACTERIZATION AND MUTATION ANALYSIS OF GOOSECOID-LIKE (GSCL), A HOMEODOMAIN-CONTAINING GENE THAT MAPS TO THE CRITICAL REGION FOR VCFS DGS ON 22Q11/, Genomics, 46(3), 1997, pp. 364-372
Authors:
MORROW BE
EDELMANN L
FERREIRA J
PANDITA RK
CARLSON CG
PROCTER JE
JACKSON M
WILSON D
GOLDBERG R
SHPRINTZEN R
KUCHERLAPATI R
Citation: Be. Morrow et al., A DUPLICATION ON CHROMOSOME 22Q11 IS THE BASIS FOR THE COMMON DELETION THAT OCCURS IN VELO-CARDIO-FACIAL SYNDROME PATIENTS, American journal of human genetics, 61(4), 1997, pp. 25-25
Authors:
SKOULTCHI AI
PUECH A
SAINTJORE B
FUNKE B
COPELAND N
JENKINS N
PANDITA R
CARLSON C
SIROTKIN H
KUCHERLAPATI R
MORROW BE
Citation: Ai. Skoultchi et al., COMPARATIVE MAPPING OF THE HUMAN AND MOUSE VCFS DGS SYNTENIC REGION DISCLOSES THE PRESENCE OF A LARGE INTERNAL REARRANGEMENT/, American journal of human genetics, 61(4), 1997, pp. 296-296
Authors:
SAINTJORE B
PUECH A
FUNKE B
SIROTKIN H
MORROW BE
KUCHERLAPATI R
SKOULTCHI AI
Citation: B. Saintjore et al., EMBRYONIC EXPRESSION OF SEVERAL GENES COMMONLY DELETED IN VCF DGS SYNDROME/, American journal of human genetics, 61(4), 1997, pp. 925-925
Authors:
FUNKE B
SAINTJORE B
PUECH A
SIROTKIN H
RAFT S
CARLSON C
PANDITA RK
KUCHERLAPATI R
SKOULTCHI A
MORROW BE
Citation: B. Funke et al., A NEW GOOSECOID GENE FAMILY MEMBER IS IN THE VCFS DGS CRITICAL REGION/, American journal of human genetics, 61(4), 1997, pp. 981-981
Authors:
CARLSON C
SIROTKIN H
PANDITA R
GOLDBERG R
MCKIE J
WADEY R
PATANJALI SR
WEISSMAN SM
ANYANEYEBOA K
WARBURTON D
SCAMBLER P
SHPRINTZEN R
KUCHERLAPATI R
MORROW BE
Citation: C. Carlson et al., MOLECULAR DEFINITION OF 22Q11 DELETIONS IN 151 VELO-CARDIO-FACIAL-SYNDROME PATIENTS, American journal of human genetics, 61(3), 1997, pp. 620-629