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American Journal of Medical Genetics
|
September 1, 1994
DK-phocomelia syndrome in a child with a long follow-up
M Urioste, L Paisán, M L Martínez-Frías
Colorectal Disease : the Official Journal of the Association of Coloproctology of Great Britain and Ireland
|
January 29, 2010
Importance of family history in colorectal cancer clinical practice
J Perea, M Ortiz, M Hidalgo, et al.
Colorectal Disease : the Official Journal of the Association of Coloproctology of Great Britain and Ireland
|
May 12, 2010
SMAD4 in early onset colorectal cancer
J Perea, M García-Nebreda, M Hidalgo, et al.
American Journal of Medical Genetics
|
March 1, 1996
Clinical/epidemiological analysis of congenital anomalies associated with diaphragmatic hernia
M L Martínez-Frías, L Prieto, M Urioste, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology
|
June 1, 2004
Concurrence of germline mutations in the APC and PTEN genes in a colonic polyposis family member
L Valle, R Rodríguez-López, M Robledo, et al.
American Journal of Medical Genetics
|
June 1, 1992
Pseudotrisomy 13 syndrome
M L Martínez-Frías, M Urioste, M Martin, et al.
Clinical Genetics
|
November 1, 1990
Endoreduplications in a family with a reciprocal translocation (9q;16p)
I Pinel, M Urioste, M L Martinez-Frias, et al.
American Journal of Medical Genetics
|
June 1, 1992
Tetra-phocomelia with multiple malformations: X-linked amelia, or Roberts syndrome, or DK-phocomelia syndrome?
J I Rodríguez, J Palacios, M Urioste, et al.
Lancet (London, England)
|
March 21, 1992
Methimazole in animal feed and congenital aplasia cutis
M L Martínez-Frías, A Cereijo, E Rodríguez-Pinilla, et al.
American Journal of Medical Genetics
|
January 30, 1995
De novo interstitial deletion q16.2q21 on chromosome 6
A Villa, M Urioste, J M Bofarull, et al.
Page
of 8
Search research articles
Search
Showing results (11-20 of 78) with videos related to
Sort By:
Page
of 8
American Journal of Medical Genetics
|
September 1, 1994
DK-phocomelia syndrome in a child with a long follow-up
M Urioste, L Paisán, M L Martínez-Frías
Colorectal Disease : the Official Journal of the Association of Coloproctology of Great Britain and Ireland
|
January 29, 2010
Importance of family history in colorectal cancer clinical practice
J Perea, M Ortiz, M Hidalgo, et al.
Colorectal Disease : the Official Journal of the Association of Coloproctology of Great Britain and Ireland
|
May 12, 2010
SMAD4 in early onset colorectal cancer
J Perea, M García-Nebreda, M Hidalgo, et al.
American Journal of Medical Genetics
|
March 1, 1996
Clinical/epidemiological analysis of congenital anomalies associated with diaphragmatic hernia
M L Martínez-Frías, L Prieto, M Urioste, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology
|
June 1, 2004
Concurrence of germline mutations in the APC and PTEN genes in a colonic polyposis family member
L Valle, R Rodríguez-López, M Robledo, et al.
American Journal of Medical Genetics
|
June 1, 1992
Pseudotrisomy 13 syndrome
M L Martínez-Frías, M Urioste, M Martin, et al.
Clinical Genetics
|
November 1, 1990
Endoreduplications in a family with a reciprocal translocation (9q;16p)
I Pinel, M Urioste, M L Martinez-Frias, et al.
American Journal of Medical Genetics
|
June 1, 1992
Tetra-phocomelia with multiple malformations: X-linked amelia, or Roberts syndrome, or DK-phocomelia syndrome?
J I Rodríguez, J Palacios, M Urioste, et al.
Lancet (London, England)
|
March 21, 1992
Methimazole in animal feed and congenital aplasia cutis
M L Martínez-Frías, A Cereijo, E Rodríguez-Pinilla, et al.
American Journal of Medical Genetics
|
January 30, 1995
De novo interstitial deletion q16.2q21 on chromosome 6
A Villa, M Urioste, J M Bofarull, et al.
Page
of 8