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M Baraitser

Showing results (141-150 of 194) with videos related to

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American Journal of Medical Genetics|May 1, 1987
Proteus syndrome: an expanded phenotypeR D Clark, D Donnai, J Rogers, et al.
Clinical Dysmorphology|July 1, 1993
An apparently new syndrome of bowed tibiae, radial anomalies, osteopenia, multiple fractures and developmental delayL S Chitty, C M Hall, P J Webb, et al.
Developmental Medicine and Child Neurology|April 1, 1990
An extended family with a dominantly inherited speech disorderJ A Hurst, M Baraitser, E Auger, et al.
Clinical Dysmorphology|May 8, 1998
Rapadilino syndrome--a non-Finnish caseS G Kant, M Baraitser, P J Milla, et al.
Clinical Dysmorphology|April 1, 1997
Selective IgG2 subclass deficiency--a marker for the syndrome of pre/postnatal growth retardation, developmental delay, hypotrophy of distal extremities, dental anomalies and eczemaS B Ainsworth, M Baraitser, R F Mueller, 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.
Neuropediatrics|August 1, 1990
Megalencephaly with dysmyelination, spasticity, ataxia, seizures and distinctive neurophysiological findings in two siblingsM G Harbord, A Harden, B Harding, et al.
Clinical Genetics|May 1, 1987
The Angelman (Happy Puppet) syndrome: is it autosomal recessive?M Baraitser, M Patton, S T Lam, et al.
Journal of Medical Genetics|January 1, 1990
De novo deletion of Xp22.2-pter in a female with linear skin lesions of the face and neck, microphthalmia, and anterior chamber eye anomaliesI K Temple, J A Hurst, S Hing, 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.
Pageof 20

Showing results (141-150 of 194) with videos related to

Sort By:
Pageof 20
American Journal of Medical Genetics|May 1, 1987
Proteus syndrome: an expanded phenotypeR D Clark, D Donnai, J Rogers, et al.
Clinical Dysmorphology|July 1, 1993
An apparently new syndrome of bowed tibiae, radial anomalies, osteopenia, multiple fractures and developmental delayL S Chitty, C M Hall, P J Webb, et al.
Developmental Medicine and Child Neurology|April 1, 1990
An extended family with a dominantly inherited speech disorderJ A Hurst, M Baraitser, E Auger, et al.
Clinical Dysmorphology|May 8, 1998
Rapadilino syndrome--a non-Finnish caseS G Kant, M Baraitser, P J Milla, et al.
Clinical Dysmorphology|April 1, 1997
Selective IgG2 subclass deficiency--a marker for the syndrome of pre/postnatal growth retardation, developmental delay, hypotrophy of distal extremities, dental anomalies and eczemaS B Ainsworth, M Baraitser, R F Mueller, 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.
Neuropediatrics|August 1, 1990
Megalencephaly with dysmyelination, spasticity, ataxia, seizures and distinctive neurophysiological findings in two siblingsM G Harbord, A Harden, B Harding, et al.
Clinical Genetics|May 1, 1987
The Angelman (Happy Puppet) syndrome: is it autosomal recessive?M Baraitser, M Patton, S T Lam, et al.
Journal of Medical Genetics|January 1, 1990
De novo deletion of Xp22.2-pter in a female with linear skin lesions of the face and neck, microphthalmia, and anterior chamber eye anomaliesI K Temple, J A Hurst, S Hing, 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.
Pageof 20