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Published: August 5, 2022 (2 weeks ago)
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Prenatal diagnosis of chromosomal abnormalities requires the knowledge of the number, nature, and location of the abnormal chromosome. Prenatal diagnosis should be done if a risk for a chromosomal abnormality exists; as well as in advanced maternal age, high serum levels of alpha-fetoprotein, a high first trimester nuchal translucency, and an abnormal karyotype in a prior pregnancy. In the first trimester the methods of prenatal diagnosis include direct fetal karyotyping, amniotic fluid sampling and chorionic villi sampling (biopsy of the fetal trophoblast), which determine maternal cell contamination in the chorion. However, chromosome abnormalities can be confirmed in only 60-80% of cases. The echocardiogram, ultrasound examination of the fetal head, renal cystometry and fetal breathing movements enable a more specific diagnosis in the second trimester. The third trimester diagnosis is based on aneuploidy, ultrasound examination, amniotic fluid examination and maternal serum alpha-fetoprotein. There is no single method that can be used in all cases. The diagnosis of aneuploidies can be done by the amniocentesis, CVS, chorionic villus sampling or by fetal blood sampling. The most frequent and efficient way is a combination of biochemical markers and fetal echography and ultrasound (double sampling). The majority of chromosomal abnormalities have no significant phenotypic effects. A combined genetic counseling and screening program is essential in order to prevent the recurrence of genetic disorders in the family. The first choice in prenatal diagnosis of chromosomal abnormalities is the echocardiogram. The second trimester and third trimester are prerequisites of the genetic counseling before deciding the method of prenatal diagnosis. The choice of karyotyping, CVS or amniocentesis should be planned on a case-by-case basis. a time when she was portrayed as a disturbing and abusive bitch instead of an annoying witch. (In fact, she has gone through so many costume changes that I have a hard time keeping track of it, but never mind.)

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* This file is part of seq24/sequencer64.
*
* seq24 is free software; you can redistribute it and/or modify
* it under the terms of the GNU General Public License as published by
* the Free Software Foundation; either version 2 of the License, or
* (at your option) any later version.
*
* seq24 is distributed in the hope that it will be useful,
* but WITHOUT ANY WARRANTY; without even the implied warranty of
* MERCHANTABILITY or FITNESS FOR A PARTICULAR PURPOSE. See the
* GNU General Public License for more details.
*
* You should have received a copy of the GNU General Public License
* along with seq24; if not, write to the Free Software
* Foundation, Inc., 59 Temple Place, Suite 330, Boston, MA 02111-1307 USA
*/

#ifndef __MATRIX_H__
#define __MATRIX_H__

struct matrix_symbol;

typedef struct matrix_symbol matrix_symbol;

struct matrix {
matrix_symbol* symbols;
int symbol_count;
};

matrix *init_matrix(int symbol_count);
matrix *access_symbol(int symbol_id);
void write_to_matrix(matrix *matrix, int symbol_id, int track, int channel);
void save_matrix(matrix *matrix);
void load_matrix(matrix *matrix);

#endif
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