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J G Hall

Showing results (381-390 of 426) with videos related to

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American Journal of Medical Genetics|January 1, 1981
Comments on the Neu-Laxova syndrome and CAD complexC I Scott, J M Louro, K M Laurence, et al.
The Journal of Pediatrics|January 1, 1974
A pattern of craniofacial and limb defects secondary to aberrant tissue bandsK L Jones, D W Smith, B D Hall, et al.
Human Genetics|June 1, 1991
Deletion of chromosome 21 and normal intelligence: molecular definition of the lesionJ R Korenberg, D K Kalousek, G Anneren, et al.
Animal Genetics|November 13, 2015
Inbreeding and purging at the genomic Level: the Chillingham cattle reveal extensive, non-random SNP heterozygosityJ L Williams, S J G Hall, M Del Corvo, et al.
American Journal of Medical Genetics|October 1, 1988
Bleeding diathesis in Noonan syndrome: a common associationD R Witt, B C McGillivray, J E Allanson, et al.
Journal of Medical Genetics|January 1, 1993
Arthrogryposis, ophthalmoplegia, and retinopathy: confirmation of a new type of arthrogryposisC T Schrander-Stumpel, C J Höweler, A D Reekers, et al.
Birth Defects Original Article Series|January 1, 1978
Hydrocephalus, agyria, retinal dysplasia, encephalocele (HARD +/- E) syndrome: an autosomal recessive conditionR A Pagon, J W Chandler, W R Collie, et al.
Annals of Human Genetics|May 1, 1989
Chromosome maps of man and mouse. IVA G Searle, J Peters, M F Lyon, et al.
Annals of the New York Academy of Sciences|June 30, 1983
Comparative aspects of the hepatobiliary transport of IgAE Orlans, J V Peppard, A W Payne, et al.
American Journal of Medical Genetics|August 1, 1990
Apparent postnatal onset of some manifestations of the Wiedemann-Beckwith syndromeD Chitayat, A Rothchild, E Ling, et al.
Pageof 43

Showing results (381-390 of 426) with videos related to

Sort By:
Pageof 43
American Journal of Medical Genetics|January 1, 1981
Comments on the Neu-Laxova syndrome and CAD complexC I Scott, J M Louro, K M Laurence, et al.
The Journal of Pediatrics|January 1, 1974
A pattern of craniofacial and limb defects secondary to aberrant tissue bandsK L Jones, D W Smith, B D Hall, et al.
Human Genetics|June 1, 1991
Deletion of chromosome 21 and normal intelligence: molecular definition of the lesionJ R Korenberg, D K Kalousek, G Anneren, et al.
Animal Genetics|November 13, 2015
Inbreeding and purging at the genomic Level: the Chillingham cattle reveal extensive, non-random SNP heterozygosityJ L Williams, S J G Hall, M Del Corvo, et al.
American Journal of Medical Genetics|October 1, 1988
Bleeding diathesis in Noonan syndrome: a common associationD R Witt, B C McGillivray, J E Allanson, et al.
Journal of Medical Genetics|January 1, 1993
Arthrogryposis, ophthalmoplegia, and retinopathy: confirmation of a new type of arthrogryposisC T Schrander-Stumpel, C J Höweler, A D Reekers, et al.
Birth Defects Original Article Series|January 1, 1978
Hydrocephalus, agyria, retinal dysplasia, encephalocele (HARD +/- E) syndrome: an autosomal recessive conditionR A Pagon, J W Chandler, W R Collie, et al.
Annals of Human Genetics|May 1, 1989
Chromosome maps of man and mouse. IVA G Searle, J Peters, M F Lyon, et al.
Annals of the New York Academy of Sciences|June 30, 1983
Comparative aspects of the hepatobiliary transport of IgAE Orlans, J V Peppard, A W Payne, et al.
American Journal of Medical Genetics|August 1, 1990
Apparent postnatal onset of some manifestations of the Wiedemann-Beckwith syndromeD Chitayat, A Rothchild, E Ling, et al.
Pageof 43