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American Journal of Medical Genetics
|
May 1, 1988
Simpson-Golabi-Behmel syndrome: follow-up of the Michigan family
J M Opitz, J Herrmann, E F Gilbert, et al.
American Journal of Medical Genetics
|
December 14, 1999
Blaschkolinear malformation syndrome in complex trisomy-7 mosaicism
E Magenis, M J Webb, B Spears, et al.
Pediatrics
|
August 1, 1989
Selected midline defect associations: a population study
M J Khoury, J F Cordero, J Mulinare, et al.
Birth Defects Original Article Series
|
January 1, 1974
The campomelic syndrome--comments
J M Opitz, M Feingold, M J Bull, et al.
American Journal of Medical Genetics
|
December 18, 1996
Autosomal recessive severe dwarfism in a Sicilian girl: a new form of osteodysplastic primordial dwarfism?
G Corsello, A Albanese, M Piccione, et al.
American Journal of Medical Genetics
|
November 6, 1995
Arthur G. Steinberg: an appreciation
F C Fraser, T Jenkins, A G Bearn, et al.
Zeitschrift Fur Kinderheilkunde
|
July 1, 1975
Syndrome of mental retardation, seizures, hypotonic cerebral palsy and megalocorneae, recessively inherited
G Neuhäuser, E G Kaveggia, T D France, et al.
Clinical Genetics
|
January 1, 1974
A woman with multiple congenital anomalies, mental retardation and mosaicism for an unusual translocation chromosome t(6;19)
P D Pallister, K Patau, S L Inhorn, et al.
Zeitschrift Fur Kinderheilkunde
|
January 1, 1972
The pathologic anatomy of the G-syndrome
E F Gilbert, C Viseskul, H W Mossman, et al.
American Journal of Medical Genetics
|
May 1, 1988
Simpson-Golabi-Behmel syndrome: an X-linked encephalo-tropho-schisis syndrome
G Neri, R Marini, M Cappa, et al.
Page
of 34
Search research articles
Search
Showing results (181-190 of 338) with videos related to
Sort By:
Page
of 34
American Journal of Medical Genetics
|
May 1, 1988
Simpson-Golabi-Behmel syndrome: follow-up of the Michigan family
J M Opitz, J Herrmann, E F Gilbert, et al.
American Journal of Medical Genetics
|
December 14, 1999
Blaschkolinear malformation syndrome in complex trisomy-7 mosaicism
E Magenis, M J Webb, B Spears, et al.
Pediatrics
|
August 1, 1989
Selected midline defect associations: a population study
M J Khoury, J F Cordero, J Mulinare, et al.
Birth Defects Original Article Series
|
January 1, 1974
The campomelic syndrome--comments
J M Opitz, M Feingold, M J Bull, et al.
American Journal of Medical Genetics
|
December 18, 1996
Autosomal recessive severe dwarfism in a Sicilian girl: a new form of osteodysplastic primordial dwarfism?
G Corsello, A Albanese, M Piccione, et al.
American Journal of Medical Genetics
|
November 6, 1995
Arthur G. Steinberg: an appreciation
F C Fraser, T Jenkins, A G Bearn, et al.
Zeitschrift Fur Kinderheilkunde
|
July 1, 1975
Syndrome of mental retardation, seizures, hypotonic cerebral palsy and megalocorneae, recessively inherited
G Neuhäuser, E G Kaveggia, T D France, et al.
Clinical Genetics
|
January 1, 1974
A woman with multiple congenital anomalies, mental retardation and mosaicism for an unusual translocation chromosome t(6;19)
P D Pallister, K Patau, S L Inhorn, et al.
Zeitschrift Fur Kinderheilkunde
|
January 1, 1972
The pathologic anatomy of the G-syndrome
E F Gilbert, C Viseskul, H W Mossman, et al.
American Journal of Medical Genetics
|
May 1, 1988
Simpson-Golabi-Behmel syndrome: an X-linked encephalo-tropho-schisis syndrome
G Neri, R Marini, M Cappa, et al.
Page
of 34