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American Journal of Medical Genetics
|
January 2, 1995
Unique de novo interstitial deletion of chromosome 17, del(17) (q23.2q24.3) in a female newborn with multiple congenital anomalies
M L Levin, L G Shaffer, Lewis RAp6, et al.
Neurology
|
June 1, 1997
DMD-specific FISH probes are diagnostically useful in the detection of female carriers of DMD gene deletions
A Voskova-Goldman, A Peier, C T Caskey, et al.
American Journal of Medical Genetics
|
December 1, 1993
Further characterization of 19 cases of rea(21q21q) and delineation as isochromosomes or Robertsonian translocations in Down syndrome
L G Shaffer, C McCaskill, V Haller, et al.
American Journal of Medical Genetics
|
April 5, 2000
Deletion (9) (p13.1 p21.1)
F Scaglia, O A Bodamer, S A Berend, et al.
American Journal of Human Genetics
|
April 1, 1992
Identification of DNA sequences flanking the breakpoint of human t(14q21q) Robertsonian translocations
E Earle, L G Shaffer, P Kalitsis, et al.
American Journal of Human Genetics
|
August 1, 1997
Is there an abnormal phenotype associated with maternal isodisomy for chromosome 2 in the presence of two isochromosomes?
L G Shaffer, C McCaskill, C A Egli, et al.
American Journal of Medical Genetics
|
September 19, 1997
Prenatal diagnosis of a fetus with a homologous Robertsonian translocation of chromosomes 15
S W Cheung, L G Shaffer, C S Richards, et al.
Clinical Genetics
|
September 17, 2003
Population data suggest that deletions of 1p36 are a relatively common chromosome abnormality
H A Heilstedt, B C Ballif, L A Howard, et al.
Human Molecular Genetics
|
September 1, 1996
Breakpoint diversity illustrates distinct mechanisms for Robertsonian translocation formation
S L Page, J C Shin, J Y Han, et al.
Prenatal Diagnosis
|
November 1, 1995
Mosaicism for trisomy 12: four cases with varying outcomes
F Z Bischoff, J Zenger-Hain, D Moses, et al.
Page
of 14
Search research articles
Search
Showing results (61-70 of 133) with videos related to
Sort By:
Page
of 14
American Journal of Medical Genetics
|
January 2, 1995
Unique de novo interstitial deletion of chromosome 17, del(17) (q23.2q24.3) in a female newborn with multiple congenital anomalies
M L Levin, L G Shaffer, Lewis RAp6, et al.
Neurology
|
June 1, 1997
DMD-specific FISH probes are diagnostically useful in the detection of female carriers of DMD gene deletions
A Voskova-Goldman, A Peier, C T Caskey, et al.
American Journal of Medical Genetics
|
December 1, 1993
Further characterization of 19 cases of rea(21q21q) and delineation as isochromosomes or Robertsonian translocations in Down syndrome
L G Shaffer, C McCaskill, V Haller, et al.
American Journal of Medical Genetics
|
April 5, 2000
Deletion (9) (p13.1 p21.1)
F Scaglia, O A Bodamer, S A Berend, et al.
American Journal of Human Genetics
|
April 1, 1992
Identification of DNA sequences flanking the breakpoint of human t(14q21q) Robertsonian translocations
E Earle, L G Shaffer, P Kalitsis, et al.
American Journal of Human Genetics
|
August 1, 1997
Is there an abnormal phenotype associated with maternal isodisomy for chromosome 2 in the presence of two isochromosomes?
L G Shaffer, C McCaskill, C A Egli, et al.
American Journal of Medical Genetics
|
September 19, 1997
Prenatal diagnosis of a fetus with a homologous Robertsonian translocation of chromosomes 15
S W Cheung, L G Shaffer, C S Richards, et al.
Clinical Genetics
|
September 17, 2003
Population data suggest that deletions of 1p36 are a relatively common chromosome abnormality
H A Heilstedt, B C Ballif, L A Howard, et al.
Human Molecular Genetics
|
September 1, 1996
Breakpoint diversity illustrates distinct mechanisms for Robertsonian translocation formation
S L Page, J C Shin, J Y Han, et al.
Prenatal Diagnosis
|
November 1, 1995
Mosaicism for trisomy 12: four cases with varying outcomes
F Z Bischoff, J Zenger-Hain, D Moses, et al.
Page
of 14