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J J Hoo

Showing results (11-20 of 93) with videos related to

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Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|September 1, 1980
[Two further cases of faciodigitogenital syndrome (author's transl)]J J Hoo
Human Genetics|September 1, 1979
A note on the XpJ J Hoo
Annales De Genetique|December 1, 1976
12P trisomy: a syndrome?J J Hoo
Clinical Genetics|June 1, 1986
Critical segment for 9p deletion syndromeJ J Hoo
Clinical Genetics|December 1, 1984
Cytogenetics of Prader-Willi syndromeJ J Hoo
Clinical Genetics|October 1, 1979
The Aarskog (facio-digito-genital) syndromeJ J Hoo
Annales De Genetique|January 1, 1986
Karyotype-phenotype analysis: 9p deletion versus 10q2 duplicationJ J Hoo
Clinical Genetics|March 1, 1986
High resolution pattern of an inverted duplication (15)J J Hoo
Human Genetics|February 15, 1979
Clinical consequence of Xp-J J Hoo
American Journal of Medical Genetics|May 9, 2001
New syndrome characterized by sparse hair, prominent nose, small mouth, micrognathia, cleft palate, crumpled upper helices, digit anomaly, and mild developmental delayF Bacha, J J Hoo
Pageof 10

Showing results (11-20 of 93) with videos related to

Sort By:
Pageof 10
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|September 1, 1980
[Two further cases of faciodigitogenital syndrome (author's transl)]J J Hoo
Human Genetics|September 1, 1979
A note on the XpJ J Hoo
Annales De Genetique|December 1, 1976
12P trisomy: a syndrome?J J Hoo
Clinical Genetics|June 1, 1986
Critical segment for 9p deletion syndromeJ J Hoo
Clinical Genetics|December 1, 1984
Cytogenetics of Prader-Willi syndromeJ J Hoo
Clinical Genetics|October 1, 1979
The Aarskog (facio-digito-genital) syndromeJ J Hoo
Annales De Genetique|January 1, 1986
Karyotype-phenotype analysis: 9p deletion versus 10q2 duplicationJ J Hoo
Clinical Genetics|March 1, 1986
High resolution pattern of an inverted duplication (15)J J Hoo
Human Genetics|February 15, 1979
Clinical consequence of Xp-J J Hoo
American Journal of Medical Genetics|May 9, 2001
New syndrome characterized by sparse hair, prominent nose, small mouth, micrognathia, cleft palate, crumpled upper helices, digit anomaly, and mild developmental delayF Bacha, J J Hoo
Pageof 10