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M A Patton

Showing results (51-60 of 110) with videos related to

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Journal of Medical Genetics|June 1, 1986
Tel Hashomer camptodactyly syndrome: report of a case with myopathic featuresM A Patton, K D McDermot, B D Lake, et al.
Journal of Medical Genetics|January 1, 1992
Autosomal dominant palmoplantar hyperkeratosis and sensorineural deafness in three generationsM Sharland, N R Bleach, P D Goberdhan, et al.
Clinical Genetics|June 1, 1986
A family with craniofrontonasal dysplasia, and fragile site 12q13 segregating independentlyD Kumar, J W Clark, C E Blank, et al.
Journal of Medical Genetics|February 1, 1987
An oculocerebral hypopigmentation syndrome: a case report with clinical, histochemical, and ultrastructural findingsM A Patton, M Baraitser, A H Heagerty, et al.
Journal of Medical Genetics|June 1, 1989
Hypertrichosis cubiti (hairy elbows) and short stature: a recognisable associationK D MacDermot, M A Patton, M J Williams, et al.
Journal of Medical Genetics|May 1, 1989
A new syndrome of autosomal recessive nephropathy, deafness, and hyperparathyroidismB D Edwards, M A Patton, S A Dilly, et al.
Developmental Medicine and Child Neurology|February 3, 2005
Psychological profile of children with Noonan syndromeD A Lee, S Portnoy, P Hill, et al.
Prenatal Diagnosis|March 1, 1986
Prenatal treatment of fetal hydrops associated with the hypertelorism-dysphagia syndrome (Opitz-G syndrome)M A Patton, M Baraitser, K Nickolaides, et al.
American Journal of Medical Genetics|September 22, 1999
Social, communicational, and behavioral deficits associated with ring X turner syndromeS El Abd, M A Patton, J Turk, et al.
American Journal of Obstetrics and Gynecology|September 19, 2000
Transcervical sampling as a means of detection of fetal cells during the first trimester of pregnancyY P Daryani, G H Barker, L K Penna, et al.
Pageof 11

Showing results (51-60 of 110) with videos related to

Sort By:
Pageof 11
Journal of Medical Genetics|June 1, 1986
Tel Hashomer camptodactyly syndrome: report of a case with myopathic featuresM A Patton, K D McDermot, B D Lake, et al.
Journal of Medical Genetics|January 1, 1992
Autosomal dominant palmoplantar hyperkeratosis and sensorineural deafness in three generationsM Sharland, N R Bleach, P D Goberdhan, et al.
Clinical Genetics|June 1, 1986
A family with craniofrontonasal dysplasia, and fragile site 12q13 segregating independentlyD Kumar, J W Clark, C E Blank, et al.
Journal of Medical Genetics|February 1, 1987
An oculocerebral hypopigmentation syndrome: a case report with clinical, histochemical, and ultrastructural findingsM A Patton, M Baraitser, A H Heagerty, et al.
Journal of Medical Genetics|June 1, 1989
Hypertrichosis cubiti (hairy elbows) and short stature: a recognisable associationK D MacDermot, M A Patton, M J Williams, et al.
Journal of Medical Genetics|May 1, 1989
A new syndrome of autosomal recessive nephropathy, deafness, and hyperparathyroidismB D Edwards, M A Patton, S A Dilly, et al.
Developmental Medicine and Child Neurology|February 3, 2005
Psychological profile of children with Noonan syndromeD A Lee, S Portnoy, P Hill, et al.
Prenatal Diagnosis|March 1, 1986
Prenatal treatment of fetal hydrops associated with the hypertelorism-dysphagia syndrome (Opitz-G syndrome)M A Patton, M Baraitser, K Nickolaides, et al.
American Journal of Medical Genetics|September 22, 1999
Social, communicational, and behavioral deficits associated with ring X turner syndromeS El Abd, M A Patton, J Turk, et al.
American Journal of Obstetrics and Gynecology|September 19, 2000
Transcervical sampling as a means of detection of fetal cells during the first trimester of pregnancyY P Daryani, G H Barker, L K Penna, et al.
Pageof 11