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N H Robin

Showing results (11-20 of 61) with videos related to

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American Journal of Medical Genetics|July 27, 2001
Disorganization in mice and humansN H Robin, J H Nadeau
Teratology|August 1, 1994
Unusual craniofacial dysmorphia due to prenatal alcohol and cocaine exposureN H Robin, E H Zackai
Postgraduate Medicine|March 23, 2000
Genetic counseling in primary care. What questions are patients likely to ask, and how should they be answered?J J Facher, N H Robin
Pediatrics in Review|April 29, 1998
Hypermobility syndromeD B Everman, N H Robin
American Journal of Medical Genetics|March 29, 1996
Opitz G/BBB syndrome: clinical comparisons of families linked to Xp22 and 22q, and a review of the literatureN H Robin, J M Opitz, M Muenke
Seminars in Pediatric Neurology|July 24, 2001
Genetic advances in central nervous system malformations in the fetus and neonateL B Jeng, R Tarvin, N H Robin
Archives of Pediatrics & Adolescent Medicine|May 30, 1998
Deletion 22q11: a newly recognized cause of behavioral and psychiatric disordersS E McCandless, J A Scott, N H Robin
Clinical Genetics|July 18, 2015
Sixteenth-century German woodcut of a male infant with possible disorganizationT F Heyne, N H Robin, A E Lin
Journal of Child Neurology|December 11, 1999
Agenesis of the corpus callosum associated with DiGeorge-velocardiofacial syndrome: a case report and review of the literatureN C Kraynack, R W Hostoffer, N H Robin
American Journal of Medical Genetics|March 15, 1996
Craniosynostosis, Philadelphia type: a new autosomal dominant syndrome with sagittal craniosynostosis and syndactyly of the fingers and toesN H Robin, B Segel, G Carpenter, et al.
Pageof 7

Showing results (11-20 of 61) with videos related to

Sort By:
Pageof 7
American Journal of Medical Genetics|July 27, 2001
Disorganization in mice and humansN H Robin, J H Nadeau
Teratology|August 1, 1994
Unusual craniofacial dysmorphia due to prenatal alcohol and cocaine exposureN H Robin, E H Zackai
Postgraduate Medicine|March 23, 2000
Genetic counseling in primary care. What questions are patients likely to ask, and how should they be answered?J J Facher, N H Robin
Pediatrics in Review|April 29, 1998
Hypermobility syndromeD B Everman, N H Robin
American Journal of Medical Genetics|March 29, 1996
Opitz G/BBB syndrome: clinical comparisons of families linked to Xp22 and 22q, and a review of the literatureN H Robin, J M Opitz, M Muenke
Seminars in Pediatric Neurology|July 24, 2001
Genetic advances in central nervous system malformations in the fetus and neonateL B Jeng, R Tarvin, N H Robin
Archives of Pediatrics & Adolescent Medicine|May 30, 1998
Deletion 22q11: a newly recognized cause of behavioral and psychiatric disordersS E McCandless, J A Scott, N H Robin
Clinical Genetics|July 18, 2015
Sixteenth-century German woodcut of a male infant with possible disorganizationT F Heyne, N H Robin, A E Lin
Journal of Child Neurology|December 11, 1999
Agenesis of the corpus callosum associated with DiGeorge-velocardiofacial syndrome: a case report and review of the literatureN C Kraynack, R W Hostoffer, N H Robin
American Journal of Medical Genetics|March 15, 1996
Craniosynostosis, Philadelphia type: a new autosomal dominant syndrome with sagittal craniosynostosis and syndactyly of the fingers and toesN H Robin, B Segel, G Carpenter, et al.
Pageof 7