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B R Elejalde

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Journal of the American Academy of Dermatology|October 1, 1994
Linear facial skin defects associated with microphthalmia and other malformations, with chromosome deletion Xp22.1A Eng, R R Lebel, B R Elejalde, et al.
Prenatal Diagnosis|December 1, 1993
45,X/46,XX/47,XXX phenotypeR R Lebel, B R Elejalde, M M de Elejalde, et al.
American Journal of Medical Genetics|July 1, 1983
Prenatal diagnosis in two pregnancies of an achondroplastic womanB R Elejalde, M M de Elejalde, P R Hamilton, et al.
Journal of Clinical Ultrasound : JCU|October 1, 1983
Diagnosis of twin to twin transfusion syndrome at 18 weeks of gestationB R Elejalde, M Mercedes de Elejalde, A M Wagner, et al.
American Journal of Medical Genetics|July 1, 1985
Prenatal diagnosis of Weyers syndrome (deficient ulnar and fibular rays with bilateral hydronephrosis)B R Elejalde, M M de Elejalde, C Booth, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|June 1, 1994
Gazali-Temple syndromeS D McLeod, J Sugar, B R Elejalde, et al.
American Journal of Medical Genetics|January 1, 1977
The trisomy 4p syndrome: case report and reviewC H Gonzalez, A Sommer, L F Meisner, et al.
American Journal of Medical Genetics|January 1, 1983
Prenatal diagnosis of cyclopiaB R Elejalde, M M de Elejalde, P R Hamilton, et al.
American Journal of Medical Genetics|August 1, 1984
Manifestations of pseudoxanthoma elasticum during pregnancy: a case report and review of the literatureB R Elejalde, M M de Elejalde, T Samter, et al.
American Journal of Medical Genetics|February 1, 1990
Prospective study of amniocentesis performed between weeks 9 and 16 of gestation: its feasibility, risks, complications and use in early genetic prenatal diagnosisB R Elejalde, M M de Elejalde, J M Acuña, et al.
Pageof 5

Showing results (31-40 of 48) with videos related to

Sort By:
Pageof 5
Journal of the American Academy of Dermatology|October 1, 1994
Linear facial skin defects associated with microphthalmia and other malformations, with chromosome deletion Xp22.1A Eng, R R Lebel, B R Elejalde, et al.
Prenatal Diagnosis|December 1, 1993
45,X/46,XX/47,XXX phenotypeR R Lebel, B R Elejalde, M M de Elejalde, et al.
American Journal of Medical Genetics|July 1, 1983
Prenatal diagnosis in two pregnancies of an achondroplastic womanB R Elejalde, M M de Elejalde, P R Hamilton, et al.
Journal of Clinical Ultrasound : JCU|October 1, 1983
Diagnosis of twin to twin transfusion syndrome at 18 weeks of gestationB R Elejalde, M Mercedes de Elejalde, A M Wagner, et al.
American Journal of Medical Genetics|July 1, 1985
Prenatal diagnosis of Weyers syndrome (deficient ulnar and fibular rays with bilateral hydronephrosis)B R Elejalde, M M de Elejalde, C Booth, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|June 1, 1994
Gazali-Temple syndromeS D McLeod, J Sugar, B R Elejalde, et al.
American Journal of Medical Genetics|January 1, 1977
The trisomy 4p syndrome: case report and reviewC H Gonzalez, A Sommer, L F Meisner, et al.
American Journal of Medical Genetics|January 1, 1983
Prenatal diagnosis of cyclopiaB R Elejalde, M M de Elejalde, P R Hamilton, et al.
American Journal of Medical Genetics|August 1, 1984
Manifestations of pseudoxanthoma elasticum during pregnancy: a case report and review of the literatureB R Elejalde, M M de Elejalde, T Samter, et al.
American Journal of Medical Genetics|February 1, 1990
Prospective study of amniocentesis performed between weeks 9 and 16 of gestation: its feasibility, risks, complications and use in early genetic prenatal diagnosisB R Elejalde, M M de Elejalde, J M Acuña, et al.
Pageof 5