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Results: 1-4 |
Results: 4
NOVEL MUTATION IN THE FGFR2 GENE AT THE SAME CODON AS THE CROUZON-SYNDROME MUTATIONS IN A SEVERE PFEIFFER-SYNDROME TYPE-2 CASE
Authors: SCHAEFER F ANDERSON C CAN B SAY B
Citation: F. Schaefer et al., NOVEL MUTATION IN THE FGFR2 GENE AT THE SAME CODON AS THE CROUZON-SYNDROME MUTATIONS IN A SEVERE PFEIFFER-SYNDROME TYPE-2 CASE, American journal of medical genetics, 75(3), 1998, pp. 252-255
2 SISTERS WITH DIFFERENT CHROMOSOMAL MICRODELETIONS - RUBINSTEIN-TAYBI-SYNDROME AND 22Q DELETION SYNDROME
Authors: CAN B QU Y JACKSON LG FLOYD M SAY B
Citation: B. Can et al., 2 SISTERS WITH DIFFERENT CHROMOSOMAL MICRODELETIONS - RUBINSTEIN-TAYBI-SYNDROME AND 22Q DELETION SYNDROME, Clinical genetics, 54(4), 1998, pp. 371-372
PRENATAL GROWTH-RETARDATION ASSOCIATED WITH MICROCEPHALY, MICROPHTHALMOS IRIS COLOBOMA AND OTHER CONGENITAL-MALFORMATIONS IN 3 SIBLINGS
Authors: CAN B
Citation: B. Can, PRENATAL GROWTH-RETARDATION ASSOCIATED WITH MICROCEPHALY, MICROPHTHALMOS IRIS COLOBOMA AND OTHER CONGENITAL-MALFORMATIONS IN 3 SIBLINGS, Clinical genetics, 52(4), 1997, pp. 250-250
HEMOPERFUSION IN AMANITA-PHALLOIDES POISONING
Authors: AJI DY CALISKAN S NAYIR A MAT A CAN B YASAR Z OZSAHIN H CULLU F SEVER L
Citation: Dy. Aji et al., HEMOPERFUSION IN AMANITA-PHALLOIDES POISONING, Journal of tropical pediatrics, 41(6), 1995, pp. 371-374
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