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Journal of Medical Genetics
|
June 1, 1986
Tel Hashomer camptodactyly syndrome: report of a case with myopathic features
M 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 generations
M Sharland, N R Bleach, P D Goberdhan, et al.
Clinical Genetics
|
June 1, 1986
A family with craniofrontonasal dysplasia, and fragile site 12q13 segregating independently
D 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 findings
M 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 association
K 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 hyperparathyroidism
B D Edwards, M A Patton, S A Dilly, et al.
Developmental Medicine and Child Neurology
|
February 3, 2005
Psychological profile of children with Noonan syndrome
D 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 syndrome
S 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 pregnancy
Y P Daryani, G H Barker, L K Penna, et al.
Page
of 11
Search research articles
Search
Showing results (51-60 of 110) with videos related to
Sort By:
Page
of 11
Journal of Medical Genetics
|
June 1, 1986
Tel Hashomer camptodactyly syndrome: report of a case with myopathic features
M 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 generations
M Sharland, N R Bleach, P D Goberdhan, et al.
Clinical Genetics
|
June 1, 1986
A family with craniofrontonasal dysplasia, and fragile site 12q13 segregating independently
D 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 findings
M 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 association
K 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 hyperparathyroidism
B D Edwards, M A Patton, S A Dilly, et al.
Developmental Medicine and Child Neurology
|
February 3, 2005
Psychological profile of children with Noonan syndrome
D 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 syndrome
S 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 pregnancy
Y P Daryani, G H Barker, L K Penna, et al.
Page
of 11