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Teratology
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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 syndrome
P Berman, C Desjardins, F C Fraser
Genetic Counseling (Geneva, Switzerland)
|
January 1, 1990
Recurrence risks for near relatives of children with sensori-neural deafness
D 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 malformations
F 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 chondrogenesis
R Seegmiller, F C Fraser, H Sheldon
The Journal of Pediatrics
|
August 1, 1976
A "community" of face-limb malformation syndromes
P Kaplan, C Cummings, F C Fraser
The Journal of Pediatrics
|
June 1, 1975
The inheritance of the Aarskog facial-digital-genital syndrome
P 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 reductase
R Rozen, F C Fraser, G Shaw
Birth Defects Original Article Series
|
January 1, 1975
Internipple distance and hand measurements in various syndromes
M Preus, M Feingold, F C Fraser
Page
of 18
Search research articles
Search
Showing results (101-110 of 172) with videos related to
Sort By:
Page
of 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 syndrome
P Berman, C Desjardins, F C Fraser
Genetic Counseling (Geneva, Switzerland)
|
January 1, 1990
Recurrence risks for near relatives of children with sensori-neural deafness
D 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 malformations
F 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 chondrogenesis
R Seegmiller, F C Fraser, H Sheldon
The Journal of Pediatrics
|
August 1, 1976
A "community" of face-limb malformation syndromes
P Kaplan, C Cummings, F C Fraser
The Journal of Pediatrics
|
June 1, 1975
The inheritance of the Aarskog facial-digital-genital syndrome
P 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 reductase
R Rozen, F C Fraser, G Shaw
Birth Defects Original Article Series
|
January 1, 1975
Internipple distance and hand measurements in various syndromes
M Preus, M Feingold, F C Fraser
Page
of 18