Search research articles
Contact Us
Filters
Showing results (31-40 of 1,120) with videos related to
Page
of 112
Sort By:
American Journal of Medical Genetics
|
January 10, 1997
Major central nervous system malformation in "micromelic dwarfism with cone epiphyses, metaphyseal dysplasia and vertebral segmentation defects"
J P Fryns
American Journal of Medical Genetics
|
July 3, 1995
Microcephaly/lymphedema and terminal deletion of the long arm of chromosome 13
J P Fryns
American Journal of Medical Genetics
|
August 23, 1996
Previously apparently undescribed syndrome: shallow orbits, ptosis, coloboma, trigonocephaly, gyral malformations, and mental and growth retardation
J P Fryns
Genetic Counseling (Geneva, Switzerland)
|
January 1, 1995
Screening for the fragile X syndrome: the necessity of international guidelines for molecular genetics predictive testing in general
J P Fryns
Annales De Genetique
|
January 1, 1992
The cardio-facio-cutaneous (CFC) syndrome and Robertsonian 15/22 translocation
J P Fryns
American Journal of Medical Genetics
|
February 1, 1994
Acalvaria and occipital scalp defects
J P Fryns
American Journal of Medical Genetics
|
April 1, 1992
Aarskog syndrome: the changing phenotype with age
J P Fryns
Genetic Counseling (Geneva, Switzerland)
|
October 20, 1998
Trisomy 9p and tetrasomy 9p: a unique, clinically recognisable syndrome
J P Fryns
American Journal of Medical Genetics
|
December 1, 1990
Follow-up of 16q deletions
J P Fryns
Progress in Clinical and Biological Research
|
January 1, 1985
X-linked mental retardation
J P Fryns
Page
of 112
Search research articles
Search
Showing results (31-40 of 1,120) with videos related to
Sort By:
Page
of 112
American Journal of Medical Genetics
|
January 10, 1997
Major central nervous system malformation in "micromelic dwarfism with cone epiphyses, metaphyseal dysplasia and vertebral segmentation defects"
J P Fryns
American Journal of Medical Genetics
|
July 3, 1995
Microcephaly/lymphedema and terminal deletion of the long arm of chromosome 13
J P Fryns
American Journal of Medical Genetics
|
August 23, 1996
Previously apparently undescribed syndrome: shallow orbits, ptosis, coloboma, trigonocephaly, gyral malformations, and mental and growth retardation
J P Fryns
Genetic Counseling (Geneva, Switzerland)
|
January 1, 1995
Screening for the fragile X syndrome: the necessity of international guidelines for molecular genetics predictive testing in general
J P Fryns
Annales De Genetique
|
January 1, 1992
The cardio-facio-cutaneous (CFC) syndrome and Robertsonian 15/22 translocation
J P Fryns
American Journal of Medical Genetics
|
February 1, 1994
Acalvaria and occipital scalp defects
J P Fryns
American Journal of Medical Genetics
|
April 1, 1992
Aarskog syndrome: the changing phenotype with age
J P Fryns
Genetic Counseling (Geneva, Switzerland)
|
October 20, 1998
Trisomy 9p and tetrasomy 9p: a unique, clinically recognisable syndrome
J P Fryns
American Journal of Medical Genetics
|
December 1, 1990
Follow-up of 16q deletions
J P Fryns
Progress in Clinical and Biological Research
|
January 1, 1985
X-linked mental retardation
J P Fryns
Page
of 112