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Results: 1-15 |
Results: 15
X-LINKED FEMALE BAND HETEROTOPIA-MALE LISSENCEPHALY SYNDROME
Authors: BERG MJ SCHIFITTO G POWERS JM MARTINEZCAPOLINO C FONG CT MYERS GJ EPSTEIN LG WALSH CA
Citation: Mj. Berg et al., X-LINKED FEMALE BAND HETEROTOPIA-MALE LISSENCEPHALY SYNDROME, Neurology, 50(4), 1998, pp. 1143-1146
PRENATAL IDENTIFICATION OF DE-NOVO MARKER CHROMOSOMES USING MICRO-FISH APPROACH
Authors: XU J FONG CT CEDRONE E SULLIVAN J WANG N
Citation: J. Xu et al., PRENATAL IDENTIFICATION OF DE-NOVO MARKER CHROMOSOMES USING MICRO-FISH APPROACH, Clinical genetics, 53(6), 1998, pp. 490-496
MUTATION ANALYSIS OF PATIENTS WITH HERMANSKY-PUDLAK-SYNDROME - A FRAMESHIFT HOT-SPOT IN THE HPS GENE AND APPARENT LOCUS HETEROGENEITY
Authors: OH J HO LL ALAMELLO S AMATO D ARMSTRONG L BELLUCCI S CARAKUSHANSKY G ELLIS JP FONG CT GREEN JS HEON E LEGIUS E LEVIN AV NIEUWENHUIS HK PINCKERS A TAMURA N WHITEFORD ML YAMASAKI H SPRITZ RA
Citation: J. Oh et al., MUTATION ANALYSIS OF PATIENTS WITH HERMANSKY-PUDLAK-SYNDROME - A FRAMESHIFT HOT-SPOT IN THE HPS GENE AND APPARENT LOCUS HETEROGENEITY, American journal of human genetics, 62(3), 1998, pp. 593-598
THE 2ND-GENERATION GLOBAL FORECAST SYSTEM AT THE CENTRAL WEATHER BUREAU IN TAIWAN
Authors: LIOU CS CHEN JH TERNG CT WANG FJ FONG CT ROSMOND TE KUO HC SHIAO CH CHENG MD
Citation: Cs. Liou et al., THE 2ND-GENERATION GLOBAL FORECAST SYSTEM AT THE CENTRAL WEATHER BUREAU IN TAIWAN, Weather and forecasting, 12(3), 1997, pp. 653-663
BRACHYDACTYLY SHORT STATURE HYPERTENSION (BILGINTURAN)-SYNDROME - REPORT ON 2 FAMILIES
Authors: CHITAYAT D GRIX A BALFE JW ABRAMOWICZ JS GARZA J FONG CT SILVER MM SALLER DN BRESNICK GH GIEDION A LACHMAN RS RIMOIN DL
Citation: D. Chitayat et al., BRACHYDACTYLY SHORT STATURE HYPERTENSION (BILGINTURAN)-SYNDROME - REPORT ON 2 FAMILIES, American journal of medical genetics, 73(3), 1997, pp. 279-285
OROFACIODIGITAL SYNDROME TYPE-IV WITH TIBIAL APLASIA
Authors: FONG CT SALLER DN KLIONSKY N DICKSON J MILLER RK METLAY LA
Citation: Ct. Fong et al., OROFACIODIGITAL SYNDROME TYPE-IV WITH TIBIAL APLASIA, American journal of human genetics, 61(4), 1997, pp. 544-544
OBJECTIVE ASSESSMENT OF OB GYN RESIDENT EDUCATION IN GENETICS/
Authors: SALLER DN GARZA J HARTMANN DM FONG CT
Citation: Dn. Saller et al., OBJECTIVE ASSESSMENT OF OB GYN RESIDENT EDUCATION IN GENETICS/, American journal of human genetics, 61(4), 1997, pp. 1107-1107
DE-NOVO MARKER CHROMOSOME IDENTIFICATION BY CHROMOSOME MICRODISSECTION, PCR, AND FISH (MICRO-FISH)
Authors: WANG N XU J ARNOLD G FONG CT HO JJ CEDRONE E
Citation: N. Wang et al., DE-NOVO MARKER CHROMOSOME IDENTIFICATION BY CHROMOSOME MICRODISSECTION, PCR, AND FISH (MICRO-FISH), Pediatric research, 39(4), 1996, pp. 877-877
SUCCESSFUL TRANSFER OF YEAST ARTIFICIAL CHROMOSOMES INTO HUMAN NEUROBLASTOMA CELL-LINES
Authors: FONG CT FOX E JOHNSON TM
Citation: Ct. Fong et al., SUCCESSFUL TRANSFER OF YEAST ARTIFICIAL CHROMOSOMES INTO HUMAN NEUROBLASTOMA CELL-LINES, Journal of cellular biochemistry, 1995, pp. 392-392
A PATIENT WITH THE VELOCARDIOFACIAL SYNDROME AND AN UNBALANCED 1-22 CHROMOSOMAL TRANSLOCATION
Authors: GARZA J FONG CT CLARK E BUZZARD C WANG N
Citation: J. Garza et al., A PATIENT WITH THE VELOCARDIOFACIAL SYNDROME AND AN UNBALANCED 1-22 CHROMOSOMAL TRANSLOCATION, American journal of human genetics, 57(4), 1995, pp. 489-489
YEAST ARTIFICIAL CHROMOSOMES AS VECTORS FOR GENE-TRANSFER INTO HUMAN NEUROBLASTOMA-CELLS
Authors: FONG CT POLLOCK S DOSTMAN H FRENCH B
Citation: Ct. Fong et al., YEAST ARTIFICIAL CHROMOSOMES AS VECTORS FOR GENE-TRANSFER INTO HUMAN NEUROBLASTOMA-CELLS, American journal of human genetics, 57(4), 1995, pp. 1956-1956
CLINICAL-DIAGNOSIS OF GENETIC-DISEASES
Authors: FONG CT
Citation: Ct. Fong, CLINICAL-DIAGNOSIS OF GENETIC-DISEASES, Pediatric annals, 22(5), 1993, pp. 277-281
MOLECULAR DIAGNOSIS OF GENETIC-DISEASES
Authors: FONG CT
Citation: Ct. Fong, MOLECULAR DIAGNOSIS OF GENETIC-DISEASES, Pediatric annals, 22(5), 1993, pp. 304-310
OTO-ONYCHO-PERONEAL SYNDROME - REPORT OF A 3RD CASE
Authors: HART PS FONG CT
Citation: Ps. Hart et Ct. Fong, OTO-ONYCHO-PERONEAL SYNDROME - REPORT OF A 3RD CASE, American journal of human genetics, 53(3), 1993, pp. 1547-1547
LOSS OF HETEROZYGOSITY FOR CHROMOSOME-1 OR CHROMOSOME-14 DEFINES SUBSETS OF ADVANCED NEUROBLASTOMAS
Authors: FONG CT WHITE PS PETERSON K SAPIENZA C CAVENEE WK KERN SE VOGELSTEIN B CANTOR AB LOOK AT BRODEUR GM
Citation: Ct. Fong et al., LOSS OF HETEROZYGOSITY FOR CHROMOSOME-1 OR CHROMOSOME-14 DEFINES SUBSETS OF ADVANCED NEUROBLASTOMAS, Cancer research, 52(7), 1992, pp. 1780-1785
Risultati: 1-15 |