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Clinical Dysmorphology|June 3, 2005
Two brothers with 22q13 deletion syndrome and features suggestive of the Clark-Baraitser syndromeElisabetta Tabolacci, Marcella Zollino, Rosetta Lecce, et al.
Avian Diseases|April 1, 1992
Molecular characterization of Salmonella enteritidis isolates from Maine poultry and poultry farm environmentsJ T Singer, H M Opitz, M Gershman, et al.
Clinical Genetics|November 1, 1976
Hypertrichosis lanuginosa in a mother and sonN Freire-Maia, J Felizali, A C de Figueiredo, et al.
Nuclear Medicine Communications|March 16, 2000
67Ga-citrate and 99Tcm-MDP for estimating the severity of vertebral osteomyelitisS Gratz, J Dörner, J W Oestmann, et al.
Fetal and Pediatric Pathology|March 17, 2005
Probable second fetus with Marles-Chudley syndrome: cardiac calcifications with ulnar deficiency and absent/hypoplastic thumbsDavid A Wada, Juliana Szakacs, Anne M Kennedy, et al.
American Journal of Medical Genetics|January 1, 1980
Multiple pterygium syndromeH Chen, C H Chang, R P Misra, et al.
Clinical Genetics|January 11, 1976
Essential tremor, nystagmus and duodenal ulceration. A "new" dominantly inherited conditionG Neuhäuser, R F Daly, N C Magnelli, et al.
American Journal of Medical Genetics. Part A|February 5, 2008
X-linked congenital ataxia: a new locus maps to Xq25-q27.1Ginevra Zanni, Enrico Bertini, Cecelia Bellcross, et al.
European Journal of Pediatrics|September 1, 1976
Chondrodysplasia punctata--rhizomelic form. Pathologic and radiologic studies of three infantsE F Gilbert, J M Opitz, J W Spranger, et al.
Nature Methods|August 17, 2010
High-resolution mapping of protein sequence-function relationshipsDouglas M Fowler, Carlos L Araya, Sarel J Fleishman, et al.
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