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J-P Fryns

Showing results (31-40 of 1,120) with videos related to

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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 13J 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 retardationJ 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 generalJ P Fryns
Annales De Genetique|January 1, 1992
The cardio-facio-cutaneous (CFC) syndrome and Robertsonian 15/22 translocationJ P Fryns
American Journal of Medical Genetics|February 1, 1994
Acalvaria and occipital scalp defectsJ P Fryns
American Journal of Medical Genetics|April 1, 1992
Aarskog syndrome: the changing phenotype with ageJ P Fryns
Genetic Counseling (Geneva, Switzerland)|October 20, 1998
Trisomy 9p and tetrasomy 9p: a unique, clinically recognisable syndromeJ P Fryns
American Journal of Medical Genetics|December 1, 1990
Follow-up of 16q deletionsJ P Fryns
Progress in Clinical and Biological Research|January 1, 1985
X-linked mental retardationJ P Fryns
Pageof 112

Showing results (31-40 of 1,120) with videos related to

Sort By:
Pageof 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 13J 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 retardationJ 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 generalJ P Fryns
Annales De Genetique|January 1, 1992
The cardio-facio-cutaneous (CFC) syndrome and Robertsonian 15/22 translocationJ P Fryns
American Journal of Medical Genetics|February 1, 1994
Acalvaria and occipital scalp defectsJ P Fryns
American Journal of Medical Genetics|April 1, 1992
Aarskog syndrome: the changing phenotype with ageJ P Fryns
Genetic Counseling (Geneva, Switzerland)|October 20, 1998
Trisomy 9p and tetrasomy 9p: a unique, clinically recognisable syndromeJ P Fryns
American Journal of Medical Genetics|December 1, 1990
Follow-up of 16q deletionsJ P Fryns
Progress in Clinical and Biological Research|January 1, 1985
X-linked mental retardationJ P Fryns
Pageof 112