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F C Fraser

Showing results (101-110 of 172) with videos related to

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Teratology|April 1, 1974
Cleft palate lateral synechia syndrome without the lateral synechia (CP plus or minus LS syndrome)M Preus, F C Fraser, W Fuhrmann
Birth Defects Original Article Series|January 1, 1974
Inheritance of the Aarskog syndromeP Berman, C Desjardins, F C Fraser
Genetic Counseling (Geneva, Switzerland)|January 1, 1990
Recurrence risks for near relatives of children with sensori-neural deafnessD Koehn, K Morgan, F C Fraser
American Journal of Medical Genetics|April 12, 2001
A man, a syndrome, a gene: Clouston's hidrotic ectodermal dysplasia (HED)F C Fraser, V M Der Kaloustian
Lancet (London, England)|July 17, 1982
Increased frequency of neural tube defects in sibs of children with other malformationsF C Fraser, A Czeizel, C Hanson
The Journal of Cell Biology|March 1, 1971
A new chondrodystrophic mutant in mice. Electron microscopy of normal and abnormal chondrogenesisR Seegmiller, F C Fraser, H Sheldon
The Journal of Pediatrics|August 1, 1976
A "community" of face-limb malformation syndromesP Kaplan, C Cummings, F C Fraser
The Journal of Pediatrics|June 1, 1975
The inheritance of the Aarskog facial-digital-genital syndromeP Berman, C Desjardins, F C Fraser
American Journal of Medical Genetics|April 6, 1999
Decreased proportion of female newborn infants homozygous for the 677 C-->T mutation in methylenetetrahydrofolate reductaseR Rozen, F C Fraser, G Shaw
Birth Defects Original Article Series|January 1, 1975
Internipple distance and hand measurements in various syndromesM Preus, M Feingold, F C Fraser
Pageof 18

Showing results (101-110 of 172) with videos related to

Sort By:
Pageof 18
Teratology|April 1, 1974
Cleft palate lateral synechia syndrome without the lateral synechia (CP plus or minus LS syndrome)M Preus, F C Fraser, W Fuhrmann
Birth Defects Original Article Series|January 1, 1974
Inheritance of the Aarskog syndromeP Berman, C Desjardins, F C Fraser
Genetic Counseling (Geneva, Switzerland)|January 1, 1990
Recurrence risks for near relatives of children with sensori-neural deafnessD Koehn, K Morgan, F C Fraser
American Journal of Medical Genetics|April 12, 2001
A man, a syndrome, a gene: Clouston's hidrotic ectodermal dysplasia (HED)F C Fraser, V M Der Kaloustian
Lancet (London, England)|July 17, 1982
Increased frequency of neural tube defects in sibs of children with other malformationsF C Fraser, A Czeizel, C Hanson
The Journal of Cell Biology|March 1, 1971
A new chondrodystrophic mutant in mice. Electron microscopy of normal and abnormal chondrogenesisR Seegmiller, F C Fraser, H Sheldon
The Journal of Pediatrics|August 1, 1976
A "community" of face-limb malformation syndromesP Kaplan, C Cummings, F C Fraser
The Journal of Pediatrics|June 1, 1975
The inheritance of the Aarskog facial-digital-genital syndromeP Berman, C Desjardins, F C Fraser
American Journal of Medical Genetics|April 6, 1999
Decreased proportion of female newborn infants homozygous for the 677 C-->T mutation in methylenetetrahydrofolate reductaseR Rozen, F C Fraser, G Shaw
Birth Defects Original Article Series|January 1, 1975
Internipple distance and hand measurements in various syndromesM Preus, M Feingold, F C Fraser
Pageof 18