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X monosomy and balanced Robertsonian translocation in a girl with Turner Syndrome
(Sociedade Brasileira de Genética, 2006-01-01)
We describe a case of X monosomy associated with a maternally inherited t(13;14) Robertsonian translocation in a girl with Turner syndrome. The girl's X chromosome was demonstrated to be maternally inherited, ruling out ...
X monosomy and balanced Robertsonian translocation in a girl with Turner Syndrome
(Sociedade Brasileira de Genética, 2006-01-01)
We describe a case of X monosomy associated with a maternally inherited t(13;14) Robertsonian translocation in a girl with Turner syndrome. The girl's X chromosome was demonstrated to be maternally inherited, ruling out ...
X monosomy and balanced Robertsonian translocation in a girl with Turner Syndrome
(Sociedade Brasileira de Genética, 2014)
Estudo citogenético em equinos para detecção de portadores de monossomia do cromossomo X
(Arquivo Brasileiro Medicina Veterinaria Zootecnia, 1996-08-01)
A cytogenetic study of 22 mares with fertility has showed that four of them had 63,X/64,XX mosaicism. The X-chromosome has presented the expected interstitial heterochromatic C - banding located in the long arm, besides ...
Estudo citogenético em equinos para detecção de portadores de monossomia do cromossomo X
(Arquivo Brasileiro Medicina Veterinaria Zootecnia, 1996-08-01)
A cytogenetic study of 22 mares with fertility has showed that four of them had 63,X/64,XX mosaicism. The X-chromosome has presented the expected interstitial heterochromatic C - banding located in the long arm, besides ...
Estudo citogenético em eqüinos para detecção de portadores de monossomia do cromossomo X
(1996-08-01)
A cytogenetic study of 22 mares with fertility has showed that four of them had 63,X/64,XX mosaicism. The X-chromosome has presented the expected interstitial heterochromatic C - banding located in the long arm, besides ...
Estudo citogenético em equinos para detecção de portadores de monossomia do cromossomo X
(Arquivo Brasileiro Medicina Veterinaria Zootecnia, 2014)
Lack of evidence for monosomy 1p36 in patients with Prader-Willi-like phenotype
(Associação Brasileira de Divulgação Científica, 2008)
Monosomy 1p36 is the most common subtelomeric microdeletion syndrome with an incidence rate estimated to be 1 in 5000 births. A hypothesis of a similarity between patients with 1p36 deletion and those with Prader-Willi ...